More jobs:
Associate II, Outsourced Manufacturing
Job in
California, Moniteau County, Missouri, 65018, USA
Listed on 2026-07-08
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-07-08
Job specializations:
-
Manufacturing / Production
Regulatory Compliance Specialist, Production QC/QA
Job Description & How to Apply Below
Associate II, Global External Manufacturing, Small Molecule Drug Substance (DS)
Location
Gilead Foster City campus
Responsibilities- Execute the network strategy; manage business execution with external manufacturing organizations and supplier performance
- Collaborate with internal/external functions within and outside PDM to achieve corporate, cross‑functional, and departmental goals
- Influence network CMO performance to achieve strategic and tactical business outcomes, including KPIs
- Coordinate inter‑ and intra‑company technical transfers
- Execute tactical management of CMOs to ensure manufacturing follows the registered process and approved Master Production Record
- Support timely resolution of manufacturing/compliance issues (deviations, complaints, out‑of‑specification investigations, Material Review Board investigations, finished product trending, and change control)
- Foster continuous improvement of production and business processes to reduce cost, improve quality, increase efficiency, and ensure sustainability
- May represent manufacturing on cross‑functional Development or Commercial CMC teams
- 4+ years of experience in a pharmaceutical/biotech organization
- BA or BS degree in science or engineering; advanced degree desirable
- MS or MBA may substitute for 1 year of relevant experience
- Salary range: $ - $
- May be eligible for discretionary annual bonus, discretionary stock‑based long‑term incentives, paid time off, and benefits package (company‑sponsored medical, dental, vision, life insurance)
Apply via the Internal Career Opportunities portal in Workday (for current employees and contractors).
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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