Quality Documentation Associate
Pharmaceutical / Medical Device Industry
The Quality Documentation Associate will support change control documentation for pharmaceutical & medical device products in accordance with company policy and procedures. Individual will be working cross-functionally with Regulatory, Documentation, Labeling, Scientist, and Validation groups.
- Experience within the pharmaceutical or medical device industries is required.
- Bachelor's degree in life science or related field preferred.
- Prior work experience managing QA Documentation.
- Prior experiencing working in a GMP environment.
- Experience with Electronic Document Management systems.
Experis is an Equal Opportunity Employer (EOE/AA)