Job Description
Fantastic opportunity for the right person to join a dynamic company in Limerick, with excellent rate and conditions. Plenty of opportunities for contract extensions.
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:
1. Proficient in process validation requirements on new manufacturing processes, equipment introductions and process changes.
2. Responsibility for carrying out process validation (IQ,OQ & PQ) by following approved standard operating procedures.
3. Experience with Good Manufacturing Practices along with all other regulatory requirements.
4. Write, and carry out reviews on all validation documentation.
Qualifications and Preferred Experience:
5. Experience in Temp Mapping, Cleaning Validation,HVAC/Utility Validation or Process Validation desirable.
6. Bachelor of Sciences degree, or higher, in a technical discipline is required.
7. 3+ years experience in a cGMP regulated manufacturing environment is essential.
8. Knowledge of equipment and utility validation, and laboratory systems / validation preferred.
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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