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Senior Project Manager

Company

Quanta part of QCS Staffing

Location

Central London, United Kingdom

Type

Contract

Key responsibilities

:
  • The final review of clinical batch records to ensure compliance with GMP and conformance with regulatory filings.
  • Compilation and approval data packs and presentation to the QP for final release.
  • Work closely with global functions supporting the clinical supply chain, as well as clinical manufacturing sites internally and externally.

    • Experience required:
  • Excellent communication skills
  • An ability to manage issue resolution
  • Confidence to work with minimal supervision
  • Existing experience in a QA role in a GMP environment

    • If this role is of interest to you, please apply now! 

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