At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuel…
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…
Job Description: At Editas, we're driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unm…
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…
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…
Do you have leadership skills and an in depth knowledge within Regulatory Affairs? Do you want to work on innovative projects of importance for our early Respiratory and Immunology…
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…