The Role: The Associate Director of Regulatory Affairs-International will play a key role in shaping the strategic direction of regulatory affairs in the LATAM region. With a focus on messenger RNA therapeutics, this individual will work with multiple teams ensuring the integration
Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries
About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to
About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with over 85 years’ experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of
Job Description Job Description The Regulatory Affairs (RA) Associate Director, Labeling will be responsible for labeling activities across programs and stages of development, with specific responsibility for the United States and the Americas and supporting global needs as required. The
Who You Are The Associate Director, Regulatory Affairs (CMC) works closely with the manufacturing department and individual program teams to ensure CMC compliance and promote overall regulatory success. The Associate Director, Regulatory Affairs (CMC) possesses strong leadership skills, broad knowledge of multiple aspects of regulatory affairs (beyond
Innova Solutions is immediately hiring for an Associate Director, Regulatory Affairs Position type: Full time Contract Duration: 6 months Location: San Rafael, CA As a Associate Director, Regulatory Affairs , you will: Job Description: Regulatory Strategy Development Lead the development, integration, execution and maintenance of
Johnson and Johnson Medical Device Companies is recruiting for an Associate Director, Regulatory Affairs - Special Projects. The preferred location for this role is Raynham, MA however remote options within United States will be considered on a case by case
Associate Director, Regulatory Labeling Remote for East Coast Candidates Meet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director of Regulatory Labeling to support their P3/commercial products.
Job Description Job Description Company Description AbbVies 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
Job Description Job Description Company Description At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care,
Job Description Job Description Company Description AbbVies 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
Job Description Job Description Company Description AbbVies 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
Job Description Job Description Company Description AbbVies 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
Role Title: Senior Manager/Associate Director, Regulatory Affairs CMC Department: Regulatory Affairs FLSA Exempt CORE VALUES Respect ● Passion ● Teamwork ● Integrity ● Honesty ● Commitment ● Collaboration ROLE SUMMARY In this role you will provide CMC strategy input, authoring, and oversight
Software Guidance & Assistance, Inc., (SGA), is searching for an Associate Director Regulatory Affairs for a FULL TIME assignment with one of our premier Pharmaceutical clients in Hawthorne, NY . US Agent for all Client products, responsible for communication between
Associate Director, Regulatory Strategy Inozyme Pharma is searching for an Associate Director, Regulatory Strategy to join their growing Regulatory Affairs team. As an Associate Director, Regulatory Strategy, this individual will be responsible for guiding regulatory strategy and leading global health authority interactions to support global development from early
Job Description Job Description The Regulatory Affairs (RA) Associate Director, Labeling will be responsible for labeling activities across programs and stages of development, with specific responsibility for the United States and the Americas and supporting global needs as required. The
Job Description Job Description About SpringWorks Therapeutics SpringWorks is a commercial-stage biopharmaceutical company applying a precision medicine approach to developing and delivering life-changing medicines for people with severe rare diseases and cancer. SpringWorks has a diversified
Job Description Job Description Company Overview Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio