- Merck (Boston, MA)
- **Job Description** We are seeking a dynamic and experienced Quality & Compliance Director to lead GMP compliance across our global network of internal and ... matter expert (SME) on current good manufacturing practices (CGMP) for pharmaceutical manufacturing, including large molecule manufacturing, guiding compliance … more
- Takeda Pharmaceuticals (Boston, MA)
- …the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the ... Management and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and… more
- Takeda Pharmaceuticals (Boston, MA)
- …and other complex diseases. The Head of Global Regulatory Affairs Operations, Compliance & Process Excellence is accountable for overseeing Global Regulatory Affairs ... PDT BU portfolio of products. As the Head of Global Regulatory Affairs Operations, Compliance & Process Excellence, you will: + Play a key strategic role in… more
- Takeda Pharmaceuticals (Boston, MA)
- …Management and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and ... monitor the health of the QMS including the identification of systematic quality compliance risks and implementation of robust mitigation plans + Engage with CPMQ… more
- Merck (Boston, MA)
- **Job Description** The Global Medical Excellence Director (GMED) reports to the Sr. Director , Global Medical Excellence, and is an experienced leader/subject ... Internal strategic excellence: In coordination with those in Executive Director Medical Affairs (EDMA), Global Director Medical...+ Extensive experience (at least 5 years) in the pharmaceutical or biotechnology industry in Medical Affairs or a… more
- Takeda Pharmaceuticals (Boston, MA)
- …of scientific communications strategy and deliverables, the **Associate Director , Scientific Communications Lead, Hematology** proactively defines and drives ... in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and implements strategic publications and… more
- Bayer (Cambridge, MA)
- …and diverse minds to make a real difference, there's only one choice.** ** Director R&D Reg Data Mgmt Expert DSAI** **YOUR TASKS AND RESPONSIBILITIES** The primary ... responsibilities of this role, Director , R&D Data Management Expert, DSAI are to: This...Chain etc. by way product data lifecycle management and compliance with evolving standards beyond 2025. Such streamlining will… more
- Sumitomo Pharma (Boston, MA)
- …of SOPs, business rules and training + In depth knowledge of pharmaceutical manufacturer compliance , patient confidentiality, product reimbursement and product ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations...highly motivated, and experienced individual for the position of ** Director , Patient & HUB Operations, Rare Disease** . The… more
- Sanofi Group (Cambridge, MA)
- …including email monitoring, live monitoring activities, and other projects in compliance with pharmaceutical industry regulations and company policies. As ... **Job Title** : Director of Monitoring, Ethics and Business Integrity **Location:**...& Business Integrity department at Sanofi, you will lead compliance monitoring activities within the US Monitoring Team. This… more
- Merck (Boston, MA)
- …decision-making at our company, this position offers an opportunity for the Director to drive pipeline impact and mentor/coach a talented group of ... pharmacometricians. The Director -Pharmacometrics will work with scientists within QP2 by proactively...increasing responsibility and independence in a similar role in pharmaceutical drug development or academia + Educational background in… more