- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the compliance ... in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Location: Cambridge, MA** **About the role:** As a Process Scientist (Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), you will provide ... Sciences + Global Manufacturing Supply, Global Quality and Global Regulatory Affairs . + SME for Takeda drug product manufacturing organization and network.… more
- Takeda Pharmaceuticals (Boston, MA)
- …submissions, ensure compliance, and enhance operational efficiency This role will coordinate with Business Systems Owners to identify value and business cases at ... level strategy and vision in collaboration with stakeholders, aligning with business goals and technology directions. Maintains and communicates the integrated… more
- Olympus Corporation of the Americas (Westborough, MA)
- …Americas. Ensures the QMS design maintenance execution and governance supports business objectives through: proactive monitoring and application of global regulatory ... + Ability to assess and develop teamtalent to support business objects and personal objects of employees. + Prioritize...local law. Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs … more
- Edwards Lifesciences (Boston, MA)
- …at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based ... with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to… more
- Pfizer (Cambridge, MA)
- …such as project leaders, research units, biostatistics, regulatory affairs , clinical pharmacology, human genetics, translational oncology, precision medicine, ... of other colleagues to achieve meaningful outcomes and create business impact. **PHYSICAL/MENTAL REQUIREMENTS** Perform complex data analysis **NON-STANDARD WORK… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …external regulations. This position reports directly to the Associate Director , CNS Scientific Communications. **Job Description** **Key Responsibilities Include:** ... Content Development** + Under the guidance of the Associate Director , Medical Communications, draft and maintain high-priority, foundational scientific communication… more
- Takeda Pharmaceuticals (Lexington, MA)
- …a technical and/or operational resource, upon the request of internal and external business partners, health care professionals (HCPs) and consumers. As part of the ... US Medical team, you will report to the Director , US Medical Information and Review. This is a.../ clinical expertise for assigned products to internal (Medical Affairs strategy teams, Therapeutic Area Units within R&D, commercial… more
- Amgen (Boston, MA)
- …team, within the Regional Medical Value Access Liaisons (MVAL) group in Scientific Affairs , reporting to a Director . Geographic region for this position is ... within the US business and majority regional accounts and select payer integrated...protocol opportunities to appropriate audiences. + Represent Amgen Scientific Affairs to designated payer & select IDN accounts. +… more
- State of Massachusetts (Boston, MA)
- …Division of Occupational Licensure (DOL), an agency within the Office of Consumer Affairs and Business Regulation (OCABR), protects consumers by making sure the ... internal progress by all state inspectors and related programs. Assist with business process assessment and software improvements to increase the collection of… more