What are the responsibilities and job description for the QC Chemist position at EPM Scientific?
A leading CDMO in Wisconsin is seeking three QC Chemists on a contract basis to provide extra support with product release testing and end product quality control activities. These positions ensure compliance with regulatory standards and contribute to the timely release of raw materials, intermediates, and finished products. Applicants must be U.S. residents - no visa sponsorship is available.
Key Responsibilities
- Conduct routine and complex analytical testing on raw materials, intermediates, and finished products
- Utilize techniques including HPLC, GC, UV‑Vis, IR, dissolution, and titration
- Review and approve analytical data generated by junior chemists
- Perform method transfer, verification, and validation activities
- Investigate OOS and OOT results, prepare technical reports, and implement CAPAs
- Ensure compliance with GMP and CDMO quality standards for product release testing
Candidate Profile
- Strong background in QC chemistry within a CDMO or pharmaceutical environment
- Hands‑on experience with analytical instrumentation and method validation
- Knowledge of GMP regulations and quality systems
- Ability to interpret complex data and provide clear, actionable conclusions
- Effective communicator with attention to detail and problem‑solving skills
Contract & Eligibility
- 6- and 12-month contracts available
- Location: Wisconsin, USA
- Must be U.S. residents - no visa sponsorship available for this role