- Regeneron Pharmaceuticals (Tarrytown, NY)
- …**In this role, a typical day might include the following:** + Lead CMC /CP product development activities from a regulatory standpoint during early phase, ... + Represent CMC /CP RA at program meetings and independently provide regulatory interpretation, position, and strategy for global CMC /CP portfolios covering… more
- AbbVie (Florham Park, NJ)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: The Associate Director in CMC Statistics is responsible for providing ... + Participate in the planning/design, conduct, analysis, and interpretation of CMC studies and regulatory submissions. Participate in establishing departmental… more
- Bristol Myers Squibb (Summit, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Title: Associate Director , Cell Therapy Comparability** **Location: Summit, NJ or ... and the ability to help patients are incredible. The ** Associate Director , Cell Therapy Comparability** will lead...outcomes, conclusions, and other critical information. + Collaborate with Regulatory CMC and other key functions to… more
- Bristol Myers Squibb (Summit, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Title: Sr. Manager / Associate Director , Global Sterility Assurance CTTO** **Location: Seattle, ... BMS with our Cell Therapy team. T he **Sr Manager/ Associate Director - Sterility Assurance, Cell therapy...they apply to Cell Therapy . + Experience with regulatory inspections and CMC + Experience with… more
- Bristol Myers Squibb (Summit, NJ)
- …. **Position Summary:** Bristol-Myers Squibb is seeking a Product Quality Leader (PQL), Associate Director of Global Product Quality to support early development ... stage development programs (vector, gene editing and cell therapy projects) to ensure regulatory compliance of GMP operations in support of the program. The PQL must… more