Job Description
I have a new exciting opportunity in Limerick for a CSV Engineer on a 12 month contract with a leading Pharmaceutical company that has plenty of work in the pipeline.
You will need to have the below to be considered for this role:
1. GMP experience is essential
2. A BS/BA in Engineering, Chemistry, or Life Sciencesor 4+ years relevant experience in a similar role that will substitute relevant education
This is an hourly rate contract offering a competitive rate.
Essential Duties and Responsibilities include, but are not limited to, the following:
3. Prepare & Review validation documentation.
4. Manage change controls and non-conformances.
5. Participate in the review of CSV procedures and polices
6. Analyze the testing results against the predetermined criteria.
7. Manage compliant computerized operations and suggests methods for the identification, implementation, and maintenance of the procedures to ensure compliance within the operation.
8. Coordinate with other departments and contractors/vendors to complete validation tasks.
9. Participate in internal and external audits.
10. Manage projects and prepares status reports using Microsoft project and other communication tools.
Education and Experience:
11. Requires BS/BA in Engineering, Chemistry, or Life Sciences with 4+ years of related experience within the fields of Automation and Computer systems and IT Infrastructure Qualification/validation; will substitute relevant experience for education.
12. Experience in a GMP environment essential.
13. Biologics experience highly desirable
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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