Cmc Regulatory Affairs Jobs in Lexington, MA

Accede Solutions Inc - Lexington, Massachusetts

Hybrid Role The Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health

from: resume-library.com - 15 days ago

Keros Therapeutics - Lexington, MA

Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, race, color...

from: Pharmadiversityjobboard.com - 22 days ago

Novo Nordisk - Lexington, MA

, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and external stakeholders including KOLs and Principal Investigators. Essential Functions

from: Pharmadiversityjobboard.com - 12 days ago

Takeda - Boston, MA, United States

Vaccines CMC where you will provide program leadership and develop CMC regulatory strategy for global vaccine programs in various stages of development. You will represent the vaccine regulatory affairs team

from: linkedin.com - 7 days ago

Novo Nordisk - Lexington, MA

, , Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal TRU and Novo Nordisk global development leadership, and external stakeholders including KOLs

from: Pharmadiversityjobboard.com - 25 days ago

Novo Nordisk - Lexington, MA

with the VP Medical/Scientific Development, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and external

from: Pharmadiversityjobboard.com - 29 days ago

Takeda - Cambridge, MA, United States

of the Regulatory Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs – Pharmaceuticals. How you will contribute: Leads the Early Development Pharmaceuticals GRA CMC

from: linkedin.com - 23 days ago

HireMinds - Watertown, MA, United States

and CMC teams and related functions, including discovery, non-clinical development, Formulation, Analytical Development, QA, and CMC Regulatory Affairs. Formal descriptions can be supplied for interested

from: linkedin.com - 10 days ago

Katalyst Healthcares & Life Sciences - Cambridge, Massachusetts

Participate in CMC project team meetings and provide Regulatory CMC support as needed, including update to the teams on follow-up actions...

from: resume-library.com - Yesterday

MapLight Therapeutics, Inc. - Burlington, MA, United States

Collaborate with CMC, Program & Portfolio Management, Clinical, and Regulatory Affairs to develop program-specific strategies for appropriate data generation in support of development candidate nomination, IND

from: linkedin.com - 29 days ago