Temp Pharma QA Associate – GMP & Documentation

A leading pharmaceutical company in Ohio is seeking a Temp-QA Associate for a temporary position in Quality Assurance. The role involves managing GxP documentation, supporting the documentation lifecycle, and developing quality-related procedures. Candidates should have a Bachelor's degree in a scientific field and 0-2 years of QA experience. Strong communication skills and knowledge of GMP regulations are essential. This is an entry-level role, ideal for motivated individuals.
The Temp Pharma QA Associate – GMP & Documentation role at Alkermes is now open for applications in Wilmington, OH, United States. The advertised compensation is 27.552 - 34.440. We aim to respond to suitable candidates as soon as possible. Full responsibilities and requirements are described in the listing above. Learn more about the Temp Pharma QA Associate – GMP & Documentation role in the description above.