Document Control Specialist at BioTalent in Beverly, Massachusetts

Posted in Other 1 day ago.

Type: full-time





Job Description:

Job Duties:
  • Manage the document control process, including creation, revision, approval, distribution, and archiving of controlled documents
  • Assign document numbers, ensure timely review and approval of documents and monitor document workflows
  • Ensure all documents are accurate, up-to-date, and readily accessible.
  • Assist in preparing and maintaining quality records, ensuring completeness, traceability, and accuracy.
  • Support internal and external audits by providing controlled documents, quality records, and other required information.
  • Collaborate with cross-functional teams to identify document gaps and recommend improvements to meet regulatory standards.
  • Manage and monitor employee training records related to controlled documents and QMS processes.
  • Facilitate training sessions to educate employees on document control policies and procedures.
  • Perform receiving and inspections of incoming materials and equipment to verify conformance with specifications and quality standards.
  • Document inspection results and initiate Non-Conformance Material Reports (NCMRs) for any discrepancies.
  • Assist with shipping, labeling, and documentation of outgoing product for traceability and accuracy
  • Participate in other quality activities as time allows, including non-product software validation, CAPAs, supplier control, equipment IQ/OQ, registration, and calibration activities
  • Professionally interacts and maintains effective and open communication with all personnel, vendors, manufacturers, and customers.
  • Adheres to all applicable department, production, and company related Operational, Safety and Human Resources policies and procedures.

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