Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an ex…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed…
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 co…
Director – Global Regulatory Affairs, CMC ** Fully Remote ** IND/CTA/NDA/BLA/MAAs ** Growing Biotech, Collaborative Culture, Good Pipeline! Location: Fully Remote, with the Globa…
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 divers…
Location: Boston, United States Job reference: R-194648 Date posted: 03/13/2024 This is what you will do: The Senior Director of Regulatory Affairs Chemistry, Manufacturing, an…
Overview The Director, RA CMC Combination Products will work cross-functionally to lead development and implementation of global combination product/Medical Devices regulatory st…
Become a member of the BioNTech Family! Based in Cambridge, MA and Gaithersburg, MD. We are committed to improving the health of people worldwide with our fundamental research an…
Location: Remote, with the Global HQ in Greater Boston, so EST or Central working hours. This role would suit an experienced RA CMC professional who wants to work in a smaller te…
Description : Location: REMOTE Overview: This role provides leadership to Invicro's Regulatory Affairs function, and will be responsible for aligning the capabilities of the …
RA CMC Director ** Remote ** Lead regulatory-CMC strategy from early- to late-phase development and NDA/MAA preparations ** SM and/or Bio Location: Full remote if in Eastern or C…
Job Description General Summary: The Director, Regulatory CMC (Chemistry Manufacturing Controls) leads a cell therapy combination product program from development through comme…
Position Summary: ultraimpact - Make a difference for those who need it most The Director, CMC QA will report to the Executive Director of CMC QA and be responsible for maintai…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed…
Location: Fully Remote (HQ on the East Coast) from most East Coast or Central Time Zone Locations including New Jersey, Pennsylvania, Massachusetts, New Hampshire, Ohio, Florida, S…
Location: Fully Remote (HQ on the East Coast) from most East Coast or Central Time Zone Locations including New Jersey, Pennsylvania, Massachusetts, New Hampshire, Ohio, Florida, S…
Main responsibilities: Leads the US regulatory activities. As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the R…
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About the Department Our Boston Research & Development hub, anchored in the greater Boston area, brings together the best minds in life science innovation. The teams located in f…
Location: Boston, United States Job reference: R-186487 Date posted: 04/01/2024 Position Summary The Senior Director of Cell Line Development (CLD) will lead and direct the pro…