Job Summary
A company is looking for a Document Control Manager to oversee GxP documentation processes across multiple sites.
Key Responsibilities
- Manage electronic document processes and ensure adherence to company policies and regulatory requirements
- Coordinate with departments to review and revise documents within specified timeframes
- Provide support and training for users of the Quality Management System (QMS) and assist during audits
Required Qualifications
- 5 or more years of relevant pharmaceutical industry experience
- Experience with regulated document control in a multi-site organization
- Familiarity with electronic QMS (MasterControl and/or TrackWise) is required
- Experience as a system manager or administrator in document management platforms
- Associates or Bachelor's Degree preferred or equivalent work experience
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