Validation Specialist: I am currently seeking an experienced Validation Engineer to join a Pharmaceutical company based in Limerick. You will be responsible for the execution, review, and approval of validation activities in a GMP regulated environment. This is an hourly rate contract position. Key Responsibilities: Proficient in process validation requirements on new manufacturing processes, equipment introductions, and process changes. Responsibility for carrying out process validation (IQ, OQ & PQ) by following approved standard operating procedures. Experience with Good Manufacturing Practices along with all other regulatory requirements. Write and carry out reviews on all validation documentation. Qualifications and Preferred Experience: Experience in Temp Mapping, Cleaning Validation, HVAC/Utility Validation, or Process Validation desirable. Bachelor of Sciences degree, or higher, in a technical discipline is required.3+ years experience in a c GMP regulated manufacturing environment is essential. Knowledge of equipment and utility validation, and laboratory systems/validation preferred. Morgan Mc Kinley is acting as an Employment Agency.
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