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Document Control Coordinator
•30 days ago
| Hours | Full-time, Part-time |
|---|---|
| Location | Saint Louis, MO Saint Louis, Missouri |
About this job
Aerotek is seeking a Quality Assurance-Document Control Specialist to work for our client in St. Louis, MO.
Job Description:
- Review batch records and SOP's for accuracy, and take careful notes/edits for all identified.
- Responsible for filling SOP's and general organization of information.
- Will be responsible for edit and review of SOP's for errors, and request revisions.
- Input SOP's into their internal database, as well as utilization of Microsoft Excel and Word.
- Review proposed or actual changes that may affect the validated status of product and process.
- Enter in data to spreadsheets and make necessary adjustments.
- Ensure that all are entered in accordance with FDA and GMP regulations.
Requirements:
- Prior document control experience, preferably within the pharmaceutical industry and GMP environment.
- Strong data entry, Microsoft Excel and Microsoft Word skills
- Knowledge of GMP and FDA regulations.
- Ability to work as part of a team and self-motivate.
About Aerotek:
Aerotek, headquartered in Hanover, Md., is a leading provider of technical, professional and industrial staffing services. Established in 1983, Aerotek is an operating company of Allegis Group, the largest provider of staffing services in the U.S. Aerotek operates a network of more than 200 non-franchised offices throughout the U.S., Canada and Europe. For more information, visit .
Aerotek is acting as an Employment Agency in relation to this vacancy.