- Fresenius Medical Center (Waltham, MA)
- …the development of global regulatory strategies for the company's pharmaceutical portfolio, including IND/CTAs, NDAs, NDSs, MAAs, etc..and other key regulatory ... Compliance: + Identify and manage regulatory risks associated with the global development and commercialization of pharmaceutical products. + Ensure compliance… more
- AbbVie (North Chicago, IL)
- …understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. ... of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-functional teams to generate, deliver,… more
- AbbVie (Irvine, CA)
- …understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. ... business strategy. Responsibilities: *Serves as an in-house expert in identification and development of consumer eye care products. As required by program needs, in… more
- University of Utah (Salt Lake City, UT)
- Details **Open Date** 08/15/2025 **Requisition Number** PRN42843B **Job Title** Director IT **Working Title** Director , Technical Projects **Job Grade** I **FLSA ... Review Date (Note - Posting may close at any time)** **Job Summary** The Director of Technical Projects will coordinate and streamline the development of Project… more
- Takeda Pharmaceuticals (Boston, MA)
- …skills to effectively collaborate with cross-functional teams + Strong knowledge of drug discovery and development processes, including preclinical and clinical ... empower you to shine? Join us as an Associate Director , Process Design & Improvement in our Cambridge office....our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being… more
- Lilly (Indianapolis, IN)
- …Active Pharmaceutical Ingredient (API) manufactured within Indianapolis Active Pharmaceutical Ingredient (IAPI) manufacturing site. The Associate Director - ... for people around the world. #WeAreLilly **Responsibilities:** The Associate Director - Quality Assurance (QA) is responsible for managing...QA is primarily responsible for the productivity and development of the QA employees, the quality of the… more
- ThermoFisher Scientific (Greenville, NC)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Position: Director , Manufacturing Science and Technology (MSAT)** **Reports To: Site ... NC** **How will you make an impact?** The MSAT Director provides scientific leadership to ensure compliance, resilience &...Subject Matter Expert (SME) in Large and Small Molecule Drug Products and directs a team of Molecular Biologists,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …position to be a Product Quality Lead (PQL), Quality Assurance, in the Pharmaceutical Development and Manufacturing (PDM) organization. The PQL is a strategic ... Quality Team. The candidate should have a scientific and technical understanding of drug development and commercialization and be able to provide effective… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- …passion for quality control and a desire to make an impact in the pharmaceutical and biotech industries? Regeneron is seeking an Associate Director / Director ... focuses on incoming component testing, functional testing for combination drug products, and raw material testing. If you thrive...we'd love to hear from you! As an Associate Director / Director , a typical day might include: +… more
- ManpowerGroup (Crystal, MN)
- We are seeking a highly experienced **Senior Pharmaceutical R&D Director ** to lead scientists and complex development programs in **oral solid dosage forms** ... development , providing leadership in technical due diligence for business development opportunities. **Qualifications** + Advanced degree in ** Pharmaceutical … more