JVT Advisors

Document Control Specialist

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Location: Milford, Massachusetts
Employment Type: Contract

Job Description

Contract Length:  6+ months

Job Summary:   Coordinates the review and revision of procedures, specifications, and forms within the electronic records system, ensuring compliance with internal procedures, and has oversight of electronic record workflows and internal archiving of GMP documents.

Responsibilities:

  • Administers, uploads, and archives training documentation in MasterControl as well as hard copies.
  • Reviewer/revisor of documents
  • Administers and maintains relevant databases, preparing and issuing reports as defined by the area as well as developing custom reports as needed
  • Provides support to site personnel to ensure documentation requirements are effectively communicated, understood and met, and that governing procedures are followed
  • Supports Regulatory Inspections and Corporate Audits

Requirements:

 

  • Associates degree in business/science or equivalent, or certification in Biotechnology
  • 1-3 years’ experience in Quality with a GMP biotech/pharmaceutical company or other similarly regulated industry
  • Strong GMP knowledge
  • Full competence with Microsoft Office, particularly Word and Excel as well as electronic document management systems

Trevor Hoffman

Technical Recruiter

Trevor recruits for JVT's Life Sciences and Technology Practices where he specializes in finding, screening, and placing top-tier industry innovators at companies across multiple markets and verticals.

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