- Abbott (Alameda, CA)
- …or technical discipline. * Minimum 8-10 years of experience in Quality Systems, Regulatory Affairs , or Quality Assurance within the medical device industry. * ... with FDA, ISO 13485, EU MDR, and other global regulatory standards. The Director will provide strategic leadership, oversee medical event reporting processes,… more
- Takeda Pharmaceuticals (Boston, MA)
- …functions across Takeda Oncology including Translational Medicine, Clinical Sciences, Global Regulatory Affairs , the Oncology Business Unit (Commercial and ... and empower you to shine? Join us as a Director , Global Program Management in our Cambridge office. At...external diagnostic partners, and supporting health authority meetings and regulatory submissions (PMAs etc). This role will partner closely… more
- Takeda Pharmaceuticals (Boston, MA)
- …Japan Payer Marketing and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global ... + Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10, EUCAN, GEM… more
- JBS USA (Greeley, CO)
- **Description** Director of Food Safety and Quality Assurance Purpose and Scope/General Summary: The JBS Fed Beef team is seeking a Director of Food Safety and ... direction for quality assurance/quality control and food safety functions. The Director interfaces, directs, advises, and supports operations at all production and… more
- Ascendis Pharma (Princeton, NJ)
- …a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR Management ... create Corrective Action and Preventative action (CAPA) as applicable. + Oversee regulatory and departmental compliance by ensuring timely processing of ICSRs in the… more
- AbbVie (North Chicago, IL)
- …of the overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's ... deliver, and disseminate high-quality clinical data supporting overall product scientific and business strategy. Responsibilities: + With appropriate supervision,… more
- AbbVie (Mettawa, IL)
- …matrixed team, which includes (but not limited to): market access, medical affairs , finance, regulatory , legal, supply operations, health economics, clinical ... development, R&D, public affairs , medical and regulatory review, patient relations,...strategic prioritization, resource distribution, and governance, taking into account regulatory and scientific nuances unique to immunology… more
- Gilead Sciences, Inc. (Foster City, CA)
- …stakeholders to establish strong working relationships with quality groups, colleagues in Regulatory Affairs , Global Trade Ops, Global Commercial Operations & ... critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as...across the US, Canada & LATAM regions. The Senior Director , Quality Assurance - Distribution will sit on the… more
- Merck (Rahway, NJ)
- …(PMO); and Administrative Professionals. **Position Description/Summary:** The GPAM Associate Director , Value & Implementation Project Manager (VIPM), is a core ... progress the R&D pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive cross-functional… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …new products. Preferred **Knowledge and skills** + Solid understanding of pharmaceutical regulatory affairs , global labeling regulatory requirements and ... (MSc, PhD or PharmD) preferred. + 10+ years of relevant pharmaceutical Labeling/ Regulatory experience. + Thorough understanding of scientific principals and … more