Job Description
Join a leading Pharmaceutical company based in Cork to support Computer System Validation on a 12 month hourly rate contract.
Key Responsibilities:
1. Accountable for maintaining full knowledge of company policies/procedures, 21 CFR Part 11, Data Integrity, GAMP
2. IQ, OQ, PQ
3. Generating Validation master plans
4. Perform all aspects of Quality Systems Management (QSM) processes (Change Control, Deviation, Corrective and Preventable Actions) as well as Validation Maintenance of computerised systems.
5. Participate in audits and inspections as a Subject Matter Expert.
6. Own, revise and maintainSOPs
7. Mentor and induct junior members of the department.
Key Requirement s:
8. Degree or Masters in computer science, engineering, or other sciences.
9. 3+ years experience in CSV
10. CAPAs and deviations experience preferred
11. Experience in a GMp environment
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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