- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Contract Management will be the site-level single point of ... catering, office coffee, vending, special events, reception, etc.) housekeeping, pest control , mail, shipping and receiving, space planning and lab services (where… more
- Regeneron Pharmaceuticals (Troy, NY)
- …with multi-cloud strategy, domain expertise in batch genealogy tracking, bioprocess monitoring, quality control data flows, process control platforms ... The Associate Director , Data Architecture will lead the design, implementation...field and/or 3+ years as Lead/Senior Data Architect in pharmaceutical /life sciences. Does this sound like you? Apply now… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , RWE Statistics Date: Oct 30, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: 64221 **Who we ... new people to make a difference with. **The opportunity** The Associate Director , Real-World Evidence (RWE) Statistics sits within Global Statistics & Data Science… more
- Lilly (Indianapolis, IN)
- …and regulatory requirements. **Basic Requirements:** + 10+ years' experience in the pharmaceutical industry in business or quality operational roles across ... better for people around the world. **Overview of Role:** The Senior Director , QMS Operational Controls will provide central oversight of Operational Controls… more
- Lilly (Glen Allen, VA)
- …startup into GMP manufacturing operations._ **Position Overview** The Senior Director is responsible for leading the site's process-facing engineering functions ... As a member of the Lilly Site Lead Team, the Senior Director contributes to shaping the site's strategic direction, building organizational capability, and… more
- Gilead Sciences, Inc. (Foster City, CA)
- … Pharmaceutical Development & Manufacturing (PDM) and partner with Quality , Supply Chain, Manufacturing, CMC Regulatory Affairs, Clinical Development and ... **Job Description:** **We are seeking a talented and highly motivated Director for our Structural Characterization team in Biologics Pivotal and Commercial… more
- Lilly (Glen Allen, VA)
- …startup into GMP manufacturing operations._ **Position Overview** The **Senior Director , Operations** is responsible for leading manufacturing operations -either ... a member of the **Lilly Site Lead Team** , the Senior Director contributes to strategic direction, organizational development, and cross-functional issue resolution.… more
- ThermoFisher Scientific (Greenville, NC)
- …of decisions and minutes. + Manage global labeling compliance activities, including quality control , FDA-508 compliance, and annual reporting requirements (US ... approvals. + **Regulatory & Cross-Functional Support** + Prepare change control documentation and deviation reports for foundational and non-foundational markets.… more
- Merck (Rahway, NJ)
- …Pharmaceutical Biology, Process Analytical Technology (PAT), Professional Networking, Quality Control Management, Regulatory Affairs Compliance, Regulatory ... and chromatography. + Collaborate with cross-functional teams, including research, development, quality control , and regulatory affairs, to ensure comprehensive… more
- GRAIL (Durham, NC)
- …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... and other relevant documentation. The role collaborates cross-functionally with Quality , Lab Operations, and other stakeholders to support regulatory strategy… more