QA Specialist (Document Control)
Want to be part of a growing, global Pharmaceutical company? This is an 11-month contract, based in Cork.
- 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
- 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 / firstname.lastname@example.org REF DocCork
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