CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions…
Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis; assessment for Annex 3 comparative table with reference EU Member States Manage exe…
Job Description Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create a…
Innova Solutions is immediately hiring a Global Regulatory CMC Manager Job Title: Global Regulatory CMC Manager Position type: Full-time Contract Duration: 09 Months Location:…
SUMMARY OF POSITION Independently authors, compiles, reviews, schedules, and submits high-quality regulatory submissions in adherence with technical document standards that are fu…
Responsibilities: Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions. These submissions include health auth…
Innova Solutions is immediately hiring for an Global Regulatory CMC Manager Tittle: Global Regulatory CMC Manager Duration: 9 months Contract Location: Lawrenceville ,NJ (onsite…
Experic is an industry-leading contract development and manufacturing organization (CDMO) and clinical trial supply services company. Our vision is to deliver innovative and scalab…
PMV Pharmaceuticals Inc. Job Description: Executive Director, Head of Regulatory Affairs Reports to: Chief Development Officer Location: Hybrid (2 days a week in Princeton, NJ o…
Job Title: Sr. Specialist, Regulatory Affairs Location: Columbus, OH Job Type: Full time Req ID: 5929 About Us: As a developer, manufacturer, and supplier of essential me…
SUMMARY OF POSITION The Sr. Manager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug developm…
SUMMARY OF POSITION The Director, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development…
About the job Our team The team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages and post marketing to support the Diab…
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About the Department Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro, NJ. We suppo…
Job Description The Biologics Analytical Research & Development department of our Company Research Laboratories Division is seeking applicants for a Principal Scientist position …
At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of …