Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Nov 15, 2019
Primary responsibilities
● Perform daily donor record file review.
● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual.
● Perform a review of donor center records.
● Perform weekly review of equipment incident logs.
● Verification and release of sample shipment.
● Perform Staging of plasma for shipment.
● Inspection and release of incoming supplies.
● Perform Weekly employee observations.
● Participate in the Quality Assurance meetings and be part of the Quality Assurance team.
● Assist the Center Quality Manager to ensure that cGMP regulations are followed.
● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met.
● Performs a review of the documentation of unsuitable test results and the disposition of the associated units.
● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties:
● Performs all product release activities.
● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
● Review of equipment records and DMS information if applicable to approve out of service machines for use.
● Review and approval of deferred donor reinstatement activities.
● Perform a review of lookback information
● Waste shipment review
● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use.
● Perform a review of medical incident reports and the applicable related documentation.
Primary Requirements
Additional Responsibilities
Is certified and maintains certification in the donor processing area.
Education
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience
Typically requires no previous related experience.
Occupational Demands
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Nov 13, 2019
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Nov 13, 2019
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Nov 13, 2019
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Nov 13, 2019
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Nov 13, 2019
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Nov 13, 2019
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
Nov 13, 2019
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors.
Main Responsibilities
1. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. 5. Ensures samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. 6. Conducts daily calibration of equipment according to SOP. Resolves calibration issues. 7. Troubleshoots equipment failures. Creates incident documentation, removes and/or replaces equipment from service. 8. Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly. Record variances. Responds to and resolves freezer and/or refrigerator alarms. 9. May provide guidance and technical training about processes and procedures to Processing Technicians and other staff as required. 10. Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. 11. Understands the policies and procedures associated with hyper immune programs at the center if applicable. 12. Maintains clean efficient work environment, and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct routine audits of these internal procedures and documentation. 13. Maintains confidentiality of all personnel, donor and center information. 14. May be cross-trained in other areas to meet the needs of the business. 15. Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. 16. Perform job-related duties as assigned. Education • High school diploma or equivalent required Experience • Minimum of three (3) months’ work experience, preferably in medical or health provider environment or equivalent combination of education and experience • Must be able to perform basic math calculations Working Conditions (physical & mental requirements) • Ability to understand, remember and apply oral and/or written instructions • Understands, remembers and communicates routine, factual information • Must be able to see and speak with customers and observe equipment operation. • Occasionally perform tasks while standing and walking up to 100% of time • Reach, bend, kneel and have high level of manual dexterity • Occasionally be required to lift and carry up to 25 pounds • Fast paced environment with frequent interruptions • Frequently exposed to hazardous chemicals, extreme temperatures and to blood borne pathogens. • Required to wear Personal Protective Equipment while performing specific tasks or in certain areas • Required to work overtime and extended hours to support center operational needs
