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