- Sanofi Group (Cambridge, MA)
- …plans. **About You** **Qualifications:** + Bachelor's degree required + 5+ years of experience in the pharmaceutical /biotech industry and/or previous leadership ... **Job Title:** Associate Director , Patient Support Services Strategy, Oncology **Location:** Cambridge, MA **About the Job** Sanofi recognizes the incredible burden… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Minimum** **Requirements/Qualifications:** + BSc Degree, preferred. BA accepted. + 8+ years of pharmaceutical industry experience. This is inclusive of ... in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment… more
- Takeda Pharmaceuticals (Boston, MA)
- …(eg MSc, PhD, PharmD, MD). BA acceptable with significant Industry experience. + Sr Director 12+ years of pharmaceutical industry experience inclusive of ... representing the regulatory function on cross-functional Global Program Teams. The Senior Director also will lead discussions of regulatory strategy with senior… more
- Sanofi Group (Cambridge, MA)
- …in life sciences, pharmacy, or a medically related field. + Minimum 10 years of experience in the pharmaceutical or biotechnology industry, including 5-6 years ... **Job Title:** Director , Global Regulatory Affairs - Global Labeling Strategy...the Job** Are you ready to shape the future of medicine? The race is on to speed up… more
- Takeda Pharmaceuticals (Lexington, MA)
- … of analytical controls and compliance + Global CMC program oversight of Pharmaceutical Sciences (PS) with management and oversight of all ... in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment… more
- Takeda Pharmaceuticals (Lexington, MA)
- …excellence within the USM. * Ensure that defined processes for development of USM-sponsored publications are implemented to ensure compliance , good publication ... productivity and efficiency, and establish business relationships to increase the value of the department work product while keeping Director , US Publications… more
- Bristol Myers Squibb (Devens, MA)
- … Director ,** **Process Implementation Lead l** eads the transition of hybrid automated cell therapy manufacturing processes from Development to operations ... people manager role drives project milestones, operational readiness, and regulatory compliance , overseeing reports in support of advanced manufacturing… more
- Takeda Pharmaceuticals (Lexington, MA)
- …BU and enterprise policies and procedures. Oversees market research regulatory and compliance guidelines and responsible for the development of processes to ... my knowledge. **Job Description** **About the role:** The Director , Customer & Business Insights leads and manages a...gastroenterology preferred + Experience on client or supplier side of industry + Experience in consulting in pharmaceutical… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership for all late-stage and commercial manufacturing processes for ... overall MSAT strategy supporting the company's portfolio, focusing on technical oversight of CDMO manufacturing operations. + Build, lead, mentor, and manage the… more
- Takeda Pharmaceuticals (Boston, MA)
- …in identifying competitive strengths, weaknesses, opportunities and threats. Advanced understanding of CI processes, methods, industry ethics and compliance , and ... experience in the healthcare industry with exposure to pharmaceutical product development. + Sound knowledge of ...are essential. + This role requires an advanced understanding of CI processes, methods, industry ethics and compliance… more