Vacancy expired!
- Will work directly with Operations, R & D, Clinical and Vendors to process, revise, issue, track, and archive GMP and Google Cloud Platform controlled documents in the electronic Document Management System (DMS).
- Manage the routing, review, approval, distribution and archival of new and revised standard operating procedures (SOPs), manufacturing batch records, Quality Control test methods/specifications and other related controlled documents in the DMS to support Operations and Quality departments.
- Oversee and manage all controlled document training and the Quality System Training records
- Provide status updates and reminders when necessary, regarding document status for new, revised and those under annual review.
- Support and maintain all Quality System documentation within the DMS for GMP and Google Cloud Platform compliance.
- Support regulatory chronologies and source document files.
- Bachelor's Degree preferred.
- Minimum 1 year of hands-on experience in performing Document Control and archival functions in the pharmaceutical/Biotech industry.
- Must have excellent computer skills and be proficient in Microsoft Office tools such as Word, Excel, Adobe Acrobat.
- Health insurance
- Casual Dress code
- 401k match
Vacancy expired!