Document Control Specialist

The Document Controls Specialist will be responsible for overseeing the administration and control of cGMP documents to ensure their accuracy, quality and integrity. Responsibilities include adhering to record retention policies, safeguarding information and retrieving data more effectively and efficiently.

• Manage and maintain document control systems and databases.
• Ensure all documents are properly stored and easily accessible.
• Coordinate with various departments to ensure document accuracy and completeness.
• Monitoring of SOPs revision status.
• Review and update documents for accuracy and completeness.
• Maintain records of document requests and retrievals.
• Assist with SIR documentation of non-conformances associated with deviations, CAPAs, investigations, customer complaints.
• Ensure proper documentation retrieval for customer requests, certifications, regulatory etc.
• Maintain consistent and documented compliance will all relevant Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements.
• Other job duties as required.