Job Description
I have an amazing opportunity for a Cleaning Validation Specialist to join a leading pharmaceutical company on a 12 month contract based in Limerick.
You will get the chance to work in a dynamic team and will need to be experienced in executing activities for cleaning validation on site and experienced in writing and approving deviations/investigations.
Key Responsibilities:
1. Generate, execute and review master cleaning validation protocols, summary reports and associated data for conformance to regulations.
2. Create and design cleaning procedures for products and manufacturing equipment
3. Lead the cleaning validation program and activities
4. Organise and carry out activities in compliance with various regulations, procedures and EHS&S requirements.
5. Initiate and apply change control activities in accordance with company procedures.
6. Create and approve appropriate documentation as required.
7. Compile documentation from contractors, suppliers, and other departments for inclusion in reports
8. Ensure Protocols have reports prepped for review and approval.
9. Track and execute exceptions, events & deviations during all activities.
10. Maintain and Update Cleaning / SIP Validation Plans
11. Generate relevant GMP documentation (e.g Protocols / SOPs, Technical Documents, Investigations)
Qualifications & Preferred Experience:
12. Bachelor's Degree in a Science / Technical discipline is required
13. 3+ years of relevant industry experience.
14. Extensive experience on writing and approving Deviations
15. Experience in GDP
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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