Job Description
Join a leader in the field of pharmaceutical science as a Quality Systems Specialist, this is a 12 month hourly rate contract based in Cork, offering a hybrid working model.
Main Responsibilities:
1. Support the digitization and automation of existing & new quality systems
2. Participate in internal audits
3. Managing the non conformances and CAPAs
4. Manage change controls
5. Supporting site inspections
6. Supporting site inductions
7. Generate metrics & reports from the quality systems
8. Ensure & support GMP compliance
Required:
9. Degree in Science or engineering
10. 3+ years experience in pharma/biotech/med device industry
11. Experience in GMP environment & working within HPRA/FDA regulated environment
12. Experience across data analytics techniques/tools such as Tableau, Spotfire, Google Analytics, Rapid Minor, or Python, and intermediate/advanced Excel will be a distinct advantage.
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
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