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70 associate director regulatory affairs jobs found

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associate director regulatory affairs
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Bausch Health
May 23, 2025
Full time
Associate Director, Regulatory Affairs
Bausch Health Bridgewater, NJ, USA
Bausch Health Companies Inc. is a global, diversified pharmaceutical company whose mission is to improve people’s lives with our pharmaceutical products. We develop, manufacture and market a range of products primarily in gastroenterology, hepatology, neurology, dermatology, dentistry, aesthetics, and international pharmaceuticals. With our leading durable brands, we are delivering on our commitments to patients, health care providers, other stakeholders and society as we build an innovative company dedicated to advancing global health.
Gilead
May 20, 2025
Full time
Associate Director, Regulatory Affairs Advertising and Promotion
Gilead Foster City, CA, USA
As a worldwide workforce we are deeply committed to helping solve some of today’s biggest healthcare challenges, offering solutions for patients suffering from life-threatening diseases such as HIV/AIDS, liver disease, oncology and respiratory disease. At our core lies a corporate culture committed to science and patients, and an employee environment that fosters innovation, diversity and a commitment to the personal and professional development of all our colleagues.       As we grow, we are continually looking to connect with outstanding individuals who are interested in joining our intellectually stimulating and socially responsible team. Successful colleagues at Gilead come from all backgrounds, have a range of perspectives and thrive in an agile and rapidly evolving environment.
AbbVie
May 13, 2025
Full time
Associate Director, Regulatory Affairs
AbbVie South San Francisco, CA, USA
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
AbbVie
May 13, 2025
Full time
Associate Director, Regulatory Affairs, Strategic Global Labeling
AbbVie North Chicago, IL, USA
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
AbbVie
May 13, 2025
Full time
Associate Director, Regulatory Affairs, Strategic Global Labeling - Combination Products and Devices
AbbVie North Chicago, IL, USA
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
Teva Pharmaceutical Industries Ltd.
May 06, 2025
Full time
Associate Director, Regulatory Affairs - West Chester, PA
Teva Pharmaceutical Industries Ltd. West Chester, PA, USA
Teva Pharmaceutical Industries Ltd. is a leading global pharmaceutical company that delivers high-quality, patient-centric healthcare solutions to millions of patients every day.
Merck
May 01, 2025
Full time
Associate Director, Regulatory Affairs Liaison- Vaccines and Infectious Disease
Merck North Wales, PA, USA
At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. 
Mayne Pharma
May 01, 2025
Full time
Associate Director, Regulatory Affairs
Mayne Pharma Raleigh, NC, USA
Mayne Pharma is seeking a self-motivated sales professional to drive the adoption of key Women’s Health products through effective relationship building with prescribers.
Zoetis
May 01, 2025
Manager/Associate Director, Regulatory Affairs - CMC
Zoetis Kalamazoo, MI, USA
Join Zoetis – and build your career with a global animal health company dedicated to supporting its customers and their businesses. Why Zoetis Zoetis has more than 60 years of experience in delivering innovative, high-quality products and services that benefit our customers. Zoetis work environment At Zoetis, we take pride in a collaborative spirit and high-performing environment where every colleague is given room to learn and grow. Your opportunities at Zoetis We invest in our people and offer diverse and exciting opportunities to make a difference in a growing global industry while shaping the future of animal health. Results that matter Our colleagues make an impact by working hand-in-hand with those who raise and care for animals to better understand and address the unique real-world challenges they face. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to...
Regeneron
May 01, 2025
Associate Director, Regulatory Affairs
Regeneron Tarrytown, NY, USA
At Regeneron, we believe in the power of original thinking. Our company is built on breakthrough ideas; which is why we foster a spirit of openness, and strive to inspire from within. We are collaborative by design and driven by curiosity. Each one of us plays an active role in transforming people’s lives through our work. Regeneron’s people make us who we are, and we are truly more than a company – we’re a community. Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the...
GlaxoSmithKline
May 20, 2025
Full time
Manager/Associate Director, CMC Regulatory Affairs
GlaxoSmithKline Waltham, MA, USA
We are a focused biopharma company. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and advanced technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/immunology and oncology).
GlaxoSmithKline
May 20, 2025
Full time
Manager/Associate Director, CMC Regulatory Affairs
GlaxoSmithKline Collegeville, PA, USA
We are a focused biopharma company. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and advanced technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/immunology and oncology).
GlaxoSmithKline
May 20, 2025
Full time
Associate Director, Global Regulatory Affairs
GlaxoSmithKline Rockville, MD, USA
We are a focused biopharma company. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and advanced technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/immunology and oncology).
Gilead
May 20, 2025
Full time
Associate Director, Analytical Regulatory Sciences, Systems & Operations in CMC Regulatory Affairs
Gilead Foster City, CA, USA
As a worldwide workforce we are deeply committed to helping solve some of today’s biggest healthcare challenges, offering solutions for patients suffering from life-threatening diseases such as HIV/AIDS, liver disease, oncology and respiratory disease. At our core lies a corporate culture committed to science and patients, and an employee environment that fosters innovation, diversity and a commitment to the personal and professional development of all our colleagues.       As we grow, we are continually looking to connect with outstanding individuals who are interested in joining our intellectually stimulating and socially responsible team. Successful colleagues at Gilead come from all backgrounds, have a range of perspectives and thrive in an agile and rapidly evolving environment.
Daiichi Sankyo Company
May 13, 2025
Full time
Associate Director, Global Regulatory Affairs Labeling
Daiichi Sankyo Company Bernards, NJ, USA
Established in 2006 by the merger of two 100-year-old Japanese pharmaceutical companies, Daiichi Sankyo, Inc. is headquartered in New Jersey. The organization includes U.S. commercial operations and global drug development. We offer a unique blend of an entrepreneurial environment and a collaborative culture, and the innovation that propels us forward comes from all corners of our company. At Daiichi Sankyo, good ideas don't just happen in the lab, but also in conference rooms, at desks and in the field, contributed both by individuals and groups.
Shionogi Pharmaceutical
May 06, 2025
Full time
Associate Director/Director, Regulatory Affairs - GDP
Shionogi Pharmaceutical Florham Park, NJ, USA
Shionogi Inc. is the U.S. subsidiary of Shionogi & Co., Ltd., a 145-year-old global pharmaceutical company with headquarters in Osaka, Japan.
Sanofi
May 01, 2025
Full time
Associate Director, US Advertising and Promotion, Global Regulatory Affairs
Sanofi Cambridge, MA, USA
Sanofi is comprised of three core business units: Specialty Care, Vaccines and General Medicines. Consumer Healthcare will become a standalone business unit. Around the world, more than 100,000 people at Sanofi are dedicated to making a difference in patients' daily lives, wherever they live, and enabling them to enjoy a healthier life.
Vertex
May 01, 2025
Associate Director/Senior Director, Regulatory Affairs Strategy
Vertex Boston, MA, USA
Vertex is a global biotechnology company that invests in scientific innovation. Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. The company has three approved medicines that treat the underlying cause of cystic fibrosis (CF) – a rare, life-threatening genetic disease — and has several ongoing clinical and research programs in CF. Beyond CF, Vertex has a robust pipeline of investigational medicines in other serious diseases where it has deep insight into causal human biology, such as sickle cell disease, beta thalassemia, pain, alpha-1 antitrypsin deficiency, Duchenne muscular dystrophy and APOL1-mediated kidney disease. The diversity and authenticity of our people is part of what makes Vertex unique, and we recognize that each employee brings diverse perspectives and strengths. By embracing those strengths and celebrating differences, we are fostering an inclusive...
Vertex
May 01, 2025
Associate Director/Director, Global Regulatory Affairs Strategy - DMD
Vertex Boston, MA, USA
Vertex is a global biotechnology company that invests in scientific innovation. Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. The company has three approved medicines that treat the underlying cause of cystic fibrosis (CF) – a rare, life-threatening genetic disease — and has several ongoing clinical and research programs in CF. Beyond CF, Vertex has a robust pipeline of investigational medicines in other serious diseases where it has deep insight into causal human biology, such as sickle cell disease, beta thalassemia, pain, alpha-1 antitrypsin deficiency, Duchenne muscular dystrophy and APOL1-mediated kidney disease. The diversity and authenticity of our people is part of what makes Vertex unique, and we recognize that each employee brings diverse perspectives and strengths. By embracing those strengths and celebrating differences, we are fostering an inclusive...
Amedisys
May 06, 2025
Clinical Manager, RN
Amedisys Covington, GA, USA
Responsible for the supervision, management, coordination and provision of quality patient care while demonstrating fiscal responsibility and maintaining the highest standards of care and ensuring compliance with all policies, procedures, and regulatory requirements. Accountable for measuring, monitoring, and managing quality of patient care, achievement of key performance indicators and organizational clinical performance. Participates in interviewing and hiring of clinical staff and responsible for management/development of the clinical staff. Assist other disciplines in coordinating activities when necessary, assuming responsibility for continuity, appropriateness and quality of services delivered. Develops, plans, implements, analyzes and organizes clinical operations for the care center. Reviews requests for services and determines patient eligibility and suitability for home care services. Works with intake in coordinating patient referrals and...
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