Located at our large molecule headquarters in RTP, North Carolina, the Senior Specialist, Quality Assurance provides essential day‑to-day QA support to the analytical laboratories. This onsite role focuses on the practical execution of core Quality Management System activities—partnering closely with laboratory teams to uphold GMP expectations, ensure compliant documentation practices, and maintain a strong state of operational control. As a key QA resource for CoA approvals, review of OOS and deviation records, and support of change activities, this position strengthens routine quality operations. The Senior Specialist contributes directly to timely, accurate quality deliverables while collaborating with existing SMEs. Solvias is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life sciences industry. Our expert team combines decades of experience with regulatory expertise across small molecules, biologics, and cell and gene therapies. Solvias offers end-to-end solutions from raw material testing to drug product release and API development for small molecules. Headquartered near Basel, Switzerland, Solvias operates six global Centers of Excellence, all adhering to the highest ISO, GMP, GLP, and FDA standards
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
251-500 employees