Job Title: CMC Demand & Supply Leader Location: Framingham, MA About the Job Within CMC function, in the Global... CMC Project Management department, the ambition is to expand a strong End to End R&D Supply Demand integrating Demand...
Lugar:
Framingham, MA | 21/08/2026 17:08:56 PM | Salario: S/. $122250 - 176583.33 per year | Empresa:
SanofiManager, CMC Regulatory Affairs - Biologics At Regeneron, we use science and innovation to develop life-changing... medicines for people with serious diseases. We are seeking a Manager, CMC Regulatory Affairs - Biologics to join our CMC...
Manager, CMC Regulatory Affairs - Biologics At Regeneron, we use science and innovation to develop life-changing... medicines for people with serious diseases. We are seeking a Manager, CMC Regulatory Affairs - Biologics to join our CMC...
. We are seeking a Manager, CMC Regulatory Affairs - Biologics to join our CMC Regulatory Affairs team, supporting our biologics... across development, submissions, and post-market programs while collaborating with Global Regulatory Affairs and CMC collaborators...
. We are seeking a Manager, CMC Regulatory Affairs - Biologics to join our CMC Regulatory Affairs team, supporting our biologics... across development, submissions, and post-market programs while collaborating with Global Regulatory Affairs and CMC collaborators...
Manager, CMC Regulatory Affairs - Biologics At Regeneron, we use science and innovation to develop life-changing... medicines for people with serious diseases. We are seeking a Manager, CMC Regulatory Affairs - Biologics to join our CMC...
degree with 3+ years related experience in pharmaceutical or biotechnology, settings. 2-4 years of CMC Regulatory Affairs... experience supporting worldwide regulations. Strong understanding of global CMC Regulatory Affairs requirements, including...
strategies with Regulatory Affairs. Review CMC sections of regulatory submissions (IND, BLA/NDA, MAA) related to DP...
products at ORIC. In this role, you will collaborate closely with colleagues across regulatory operations, quality, CMC... and track regulatory submission timelines. Collaborate cross-functionally with regulatory operations, quality, CMC, nonclinical...
of GxP quality systems across QA, Clinical Ops, CMC, and Research, ensuring full compliance with 21 CFR Part 11 and modern...