What are the responsibilities and job description for the Validation Engineer position at Technical Source?
Technical Source is currently in search of a Validation Engineer for our pharmaceutical manufacturing client in the Petersburg, VA area. The qualified candidate will have experience writing and executing validation protocols for API manufacturing equipment such as Bioreactors, Filtration, and Clean Utility systems.
Responsibilities of the Validation Engineer include:
- Execution of validation protocols (IQ/OQ) for PLC based controls systems
- 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 Engineer include:
- 5 years of experience in the qualification of Upstream and Downstream process and lab equipment
- Experience with cGMP documentation review and execution
- Bachelor’s or Associates degree in related field preferred
Salary : $100,000 - $140,000
