- Location
- Holly Springs, NC
- Job Type
- Contract
- Duration
About the Role
Technical Source is currently in search of a CQV Engineer for a biopharmaceutical manufacturing client in the Holly Springs, NC area. This is a long-term contract position that requires on-site work. The qualified candidate will support the Commissioning, Qualification and Validation of process equipment, utilities and facility systems in a cGMP environment.
Responsibilities of the CQV Engineer include
- Develop and execute commissioning and qualification protocols (IQ/OQ/PQ) for process equipment, utilities and HVAC
- Perform field walkdowns, punch lists and turnover package reviews
- Conduct temperature mapping and support automation (BAS/DeltaV) testing
- Manage deviations and discrepancies and write summary reports
- Use paperless validation software (KNEAT or similar)
- Work with Engineering, Quality and Operations to meet project milestones
Qualifications of the CQV Engineer include
- Bachelor's degree in Engineering or a related field
- 3+ years of CQV experience in pharmaceutical or biotech manufacturing
- Working knowledge of cGMP, GDP and the validation life cycle (ASTM E2500 a plus)
- Experience with KNEAT or another paperless validation system preferred
*No C2C or sponsorship is available at this time*
*Compensation will scale based on experience and fit*
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