Job Title: Validation Specialist
We are seeking an experienced Validation Engineer to join our team at a Pharmaceutical company in Limerick. As a Validation Specialist, you will be responsible for executing, reviewing and approving validation activities in a GMP regulated environment.
About the Role:
* Proficient in process validation requirements on new manufacturing processes, equipment introductions and process changes.
* Responsible 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.
Requirements:
* 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 cGMP regulated manufacturing environment is essential.
* Knowledge of equipment and utility validation, and laboratory systems / validation preferred.
This is an hourly rate contract position offering excellent conditions and opportunities for contract extensions.