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 the Raleigh, NC area. This is a long-term, on-site contract position with potential for full-time conversion. The ideal candidate will have equipment validation experience writing and executing validation / qualification protocols for automated manufacturing equipment and lab 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 :
No C2C or Sponsorship is available at this time
Compensation will scale based on experience and fit
