This job listing has expired and the position may no longer be open for hire.

Document Control Specialist, Quality - 2nd Shift at Amneal Pharmaceuticals LLC (J0P)

Posted in Manufacturing 30+ days ago.

Type: Full-Time
Location: Piscataway, New Jersey





Job Description:

Job Summary

The document control specialist is responsible for administering the processes and practices which support documentation compliance. The Specialist will work in a pharmaceutical production facility and in close collaboration with Quality Assurance, Quality Control and Production with a key-focus on documentation accuracy, quality and integrity.

Essential Functions


  • Manage document control processes thru electronic systems and/ or paper base systems. Distribute approved documentation to appropriate personnel, track receipt of documentation and notebooks.

  • Maintaining lists and postings required for both electronic and hard copy; maintain specific databases in Document Control Department and training records.

  • Perform data entry and management in systems (Document Compliance and Process Compliance) and maintain the print/soft copies for all documents.

  • Collaborate with teams to complete, maintain an up-to-date Document Control Systems.

  • Store, archive, and retrieve the version documents such as certificate of analysis of materials and products, specifications, methods, protocols, and report files.

  • Prepare and distribute PBRs, Packaging Batch Records, SOPs, methods and protocols, and other controlled documents.

  • Distribute approved documentation to appropriate personnel, track receipt of documentation and notebooks. Track document approvals and any related activities and ensure on-line documents are updated and accurate.

  • Work with other departments to clarify and correct documentation to ensure compliance.

  • Organize and maintain the work area and keep up-to-date files

Additional Responsibilities


  • Prepare documentation for third party inspection/audits.

  • Assist validation and regulatory department for documentation and for their various requirements.

Education


  • Associate Degree - Preferred

Work Experience


  • Less than one year in manufacturing - Preferred

Skills and Abilities


  • 2 years of QA Documentation - Intermediate

  • cGMP and computer skills (MS Word, Access and Excel) - Advanced

  • Multitasking and flexibility to accommodate changing priorities. - Advanced

Specialized Knowledge


  • cGMP, Computer Skills (MS Word, Excel, Access)





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