What are the responsibilities and job description for the Validation Engineer position at Technical Source?
Technical Source is actively seeking a Validation Engineer for our pharmaceutical manufacturing client in Marion, North Carolina . This is a long-term, on-site contract position with the potential for full-time conversion. The ideal candidate will have experience in equipment validation, including writing and executing validation and qualification protocols for automated manufacturing and laboratory equipment.
Responsibilities of the Validation Engineers can include :
- Execution of validation protocols (IQ / OQ / PQ) for automated manufacturing equipment and lab equipment
- Authors cGMP risk assessments, user requirements & functional specifications, validation plans, protocols (i.e. IQ, OQ, PQ), traceability matrices, reports, addendums, decommissioning plans and other validation deliverables as required by the site validation SOPs.
- Complete appropriate cGMP documentation throughout validation life cycle
Qualifications of the Validation Engineers should include :
