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QA Specialist (Document Control)

Job description

QA Specialist  (Document Control)

Want to be part of a growing, global Pharmaceutical company? This is an 11-month contract, based in Cork.

Job responsibilities:

  • Responsible for the QC Labs Documentation System including Issuance, reconciliation, storage, archiving of cGMP documentation to support testing
  • Complete documentation audits
  • Responds to non-standard requests from customer needs
  • Ability to collate and control GMP documentation

Job requirements:

  • Qualification in a quality discipline is required
  • 1-2 years pharmaceutical documentation experience

If you would like to discuss this role, reach out to Louise Whitty on 021 2359140 / lwhitty@sigmar.ie REF DocCork

 

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