Reference Code
CK2565

Due to large scale project wins we now wish to recruit a QA Validation Lead to join a highly skilled PM Group team based onsite with a Biotech client in Cork

Due to large scale project wins we now wish to recruit a QA Validation Lead to join a highly skilled PM Group team based onsite with a Biotech client in Cork.  The successful candidate will have a QA background with a strong knowledge of cGMP and 21 CFR part 11 regulations to assist with C&Q documentation

Responsibilities will include:

  • Review and approval of C&Q protocols
  • Ensure highest industry standards are incorporated into C&Q activities and documentation
  • Where necessary, highlight non-compliance within C&Q documentation to ensure industry best practices and PM Group standards are maintained

Requirements:

  • Educated to Degree level in Engineering or Science related area
  • 5+ years’ experience in the pharmaceutical sector 
  • Signification experience in a QA / document  review role
  • Excellent oral and written communication skills in English
  • High level of customer orientation/understanding

Please Note

All CV’s are treated in the strictest confidence.
Recruitment agencies need not apply.

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CK2565 QA Validation Lead - CK2565

Cork, Ireland

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