- Takeda Pharmaceuticals (Lexington, MA)
- …all information I submit in my employment application is true to the best of my knowledge. **Job Description** **Associate Director , Clinical Research, Value & ... applicable. **_DIMENSIONS AND ASPECTS_** **Technical/Functional Expertise** + Comprehensive understanding of the pharmaceutical industry and regulations governing… more
- Takeda Pharmaceuticals (Boston, MA)
- …2 years in PV/safety OR clinical development preferred + Minimum 3 years of pharmaceutical industry/drug development experience + Pharmaceutical industry ... shine? Join us as a PV Risk Management Scientist/Associate Director . At Takeda, we are transforming the pharmaceutical...for excellence in everything we do. As an Associate Director / PV Risk Management Scientist, being part of… more
- Merck (Boston, MA)
- …+ In-depth expertise in local regulatory frameworks, ethical standards, and pharmaceutical compliance requirements. + Proven capability to cultivate and ... Executive Leadership, Medical Affairs, Oncology, People Leadership, People Management, Pharmaceutical Compliance , Scientific Communications, Scientific Exchange, Strategic… more
- Sumitomo Pharma (Boston, MA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of Executive Director , Commercial Manufacturing. This role is responsible for ... the successful delivery of SMPA's commercial portfolio of products. The Executive Director will lead...expert in regulatory interactions. + Maintain a high level of safety, compliance , and efficiency to drive… more
- Sumitomo Pharma (Boston, MA)
- …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Director , Regulatory Advertising & Promotion** . The Director ... Compliance , and Medical Affairs. + Provide appropriate oversight of promotional material review and ensure on-time and accurate...+ 8 - 12 years experience in biotech or pharmaceutical industry with minimum of 8 years… more
- Takeda Pharmaceuticals (Lexington, MA)
- … of comparator drugs within Global Clinical Supply Chain (GCSC). Under the direction of the Director of Centralized Ancillary and Commercial Drug Product, ... processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information...empower you to shine? Join us as an Associate Director , Vendor Management (Commercial Product Sourcing) based in Lexington,… more
- Fresenius Medical Center (Waltham, MA)
- …Identify and manage regulatory risks associated with the global development and commercialization of pharmaceutical products. + Ensure compliance with local ... **PURPOSE AND SCOPE:** Responsible for leading the strategic direction and execution of regulatory strategies for our global pharmaceutical portfolio. This… more
- Bristol Myers Squibb (Devens, MA)
- …+ Expertise in GMP compliance , global regulations, and strong understanding of pharmaceutical product development lifecycle, with specific emphasis on gene ... The Sr. Director m onitors commercial operations through periodic reviews of process and method performance, including Annual Product Quality Reviews as well as… more
- AbbVie (Waltham, MA)
- …devices to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies ... partnership with senior leadership to develop a clear picture of overall compliance state and linking this...interaction with regulatory inspectors. Direct Plant experience in a pharmaceutical setting with a minimum of 5… more
- United Therapeutics (Boston, MA)
- …details are as follows:** Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our ... provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that...appropriately respond to those needs + Facilitate a culture of accountability and compliance through ongoing cadence… more
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