Job Description

 
  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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Senior Project Manager

Job Description

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