- Sanofi Group (Cambridge, MA)
- About the Role The Associate Director , US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the ... for the advertising and promotion of prescription drugs and biologics . Essential Functions + Represents Global Regulatory ...and biologics . Essential Functions + Represents Global Regulatory Affairs (US RA AdPromo) as a member of… more
- Sanofi Group (Cambridge, MA)
- … environment and updating of standards and processes related to drug and biologics regulations + Ensure that respective regulatory team members have the ... the job** **Our team** The team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages and post marketing to… more
- Sanofi Group (Cambridge, MA)
- … environment and updating of standards and processes related to drug and biologics regulations + Ensure that respective regulatory team members have the ... **Main responsibilities:** + Leads the US regulatory activities. + As a key member of...+ Understanding of clinical development of drugs and/or innovative biologics products + Demonstrated significant leadership experience with driving… more
- Sanofi Group (Cambridge, MA)
- The Associate Director RA serves as the regulatory lead on Review Committees (RCs). As the RC RA representative, work with brands on competitively ... Industry Guidelines for the advertising and promotion of prescription drugs, biologics , and devices. **ESSENTIAL FUNCTIONS** + Provide regulatory leadership… more
- Bristol Myers Squibb (Cambridge, MA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Scientific Associate Director , DMPK Project Representative** Challenging. Meaningful. ... across the globe. PCO is looking for a Scientific Associate Director to join the Dev DMPK...activities of multiple projects; be responsible for preparation of regulatory dossier/responses; and assist in developing strategy for the… more
- AbbVie (Worcester, MA)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Quality Control provides leadership and direction to the ... Quality Function they are responsible for within Operations. This Associate Director , Quality Control is responsible for the effective implementation of AbbVie… more
- Bristol Myers Squibb (Devens, MA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director (AD) Quality Product Lead (eg, QPL, Quality ... Quality representative for the lifecycle of commercial products/brands for the Biologics /Sterile Fill and Pharma business units. The QPL, Product Quality, will… more
- Merck (Boston, MA)
- …Pharmacology and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global Clinical ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- AbbVie (Worcester, MA)
- …YouTube and LinkedIn. Job Description AbbVie Bioresearch Center (ABC) is hiring an Associate Director Automation & Manufacturing Systems position to lead the ... working in a proactive and motivating team environment. The Associate Director Automation & Manufacturing position will...opportunity to lead a technical team within a multi-product biologics manufacturing facility. In this role, as head of… more
- Sanofi Group (Framingham, MA)
- …Culture Development department within CCD located in Framingham, MA in the role of Associate Director . We are looking for a candidate with excellent scientific, ... and high productivity cell culture processes for Sanofi's very diverse early and late-stage biologics pipeline. Sanofi is looking for a leader in the field of cell… more
- Takeda Pharmaceuticals (Boston, MA)
- …help manage departmental and cross-functional teams occasionally. You will report to The Associate Director of QC Support. **How you will contribute:** + ... lead technical rigor + Knowledge of cGMP and other regulatory requirements related to manufacturing of biologics ...other regulatory requirements related to manufacturing of biologics and monoclonal antibodies. + Strong technical skills and… more