Validation Engineer | Roscommon | 2-Year FTC
About Your New Employer
An established pharmaceutical manufacturing company in Co. Roscommon is looking to recruit a Validation Engineer on a 2-year fixed-term contract.
This is a hands-on role within a regulated GMP pharmaceutical environment, with responsibility across a broad range of site validation activities.
About Your New Job
As a Validation Engineer, you will:
- Support and manage equipment qualification (IQ/OQ/PQ) activities, including protocols and reports.
- Coordinate process and cleaning validation activities.
- Support Computer System Validation (CSV) activities.
- Maintain validation documentation, including the Validation Master Plan, protocols, reports and SOPs.
- Support the site's calibration programme and associated documentation.
- Investigate validation-related deviations and support CAPA and change control.
- Support qualification of new equipment and periodic equipment reviews.
- Provide validation support during regulatory and customer audits.
- Work with Quality, Engineering and Production to deliver validation activities to agreed timelines.
What You Need
- Previous Validation Engineer experience within a pharmaceutical GMP environment.
- Strong knowledge of equipment, process and cleaning validation, including IQ/OQ/PQ.
- Good understanding of GMP, validation documentation and calibration.
- Strong technical writing, organisational and communication skills.
What’s Next?
For more information on this 2-year FTC Validation Engineer opportunity in Co. Roscommon, contact Tina at Sigmar Recruitment for a confidential discussion.
