- Teva Pharmaceuticals (West Chester, PA)
- CMC Biologics Quality Control Director, Physichemical Testing Date: Nov 15, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... CMC organization Design, plan, organize, analyze, and evaluate key elements of Biologics CMC QC strategy Specialized Knowledge: LIMS, TrackWise or VEEVA … more
- Merck (Rahway, NJ)
- …(DCT) leader is accountable for delivering a fully integrated stage-appropriate CMC development and commercialization strategy which yields the target commercial ... product. The specific role will be responsible for advancing the company's biologics portfolio. Correspondingly, the DCT leader will be responsible for delivering… more
- Gilead Sciences, Inc. (Foster City, CA)
- …+ Recruit and hire new talent. + Accountable for: + Defining critical quality attributes (CQAs) across the late-phase biologics portfolio and building deep ... across Gilead Pharmaceutical Development & Manufacturing (PDM) and partner with Quality , Supply Chain, Manufacturing, CMC Regulatory Affairs, Clinical… more
- AbbVie (North Chicago, IL)
- …transfer. + Experience in managing third party manufacturers. + Experience with quality risk management and drug product control strategies. Additional ... Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Biologics Drug Product Development (Bio DPD), a part of Development… more
- Genentech (Oceanside, CA)
- …related discipline. + 15+ years of experience in the bio-pharmaceutical industry, ie biologics manufacturing, development or related CMC functions, with at least ... **The Position** The PTD Global Biologics organization plays a pivotal role in the...DS/DP Process Equipment, Analytical Instrumentation for Process Monitoring and Control , AI applications, and Process Modeling. The role also… more
- Parexel (Providence, RI)
- …and post-approval changes Cross-Functional Collaboration * Partner with manufacturing, quality , and external organizations to address CMC -related issues ... highly motivated professional to join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior/Consultant. This role is critical to ensure our client's… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …Regulatory Submission support for US FDA and other Health Authorities. + Ensures all Quality by Design (QbD) and Design Control activities related to drug ... support of company clinical trials. + Collaborates with other external functions on CMC matters (eg, Quality , Commercial, Regulatory Affairs, etc.). Ensures the … more
- Boehringer Ingelheim (Duluth, GA)
- …alignment with corporate goals. + Defines, plans, and oversees the development of high- quality CMC regulatory submissions, with a focus on securing timely ... with Quality , R&D and Operations/Manufacturing. The Director, Scientific Expert CMC provides subject matter expertise in functional areas related to, and driven… more
- AbbVie (North Chicago, IL)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description AbbVie Biologics Analytical Research & Development ( Biologics ARD) is a ... global analytical sciences organization responsible for all CMC analytical activities related to the development of AbbVie's therapeutic biologic products. Our scope… more
- Amgen (Thousand Oaks, CA)
- …patients while transforming your career. **Process Development Senior Scientist - Pivotal Biologics Drug Substance Technology** **What you will do** Let's do this. ... at Amgen develops, characterizes and supports the commercialization of biologics drug substance manufacturing processes for all late-stage programs across… more
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