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i-Pharm GxP · Lebanon, Indiana
Initial 12-month contract, with extensions anticipated
Fully onsite in Lebanon, Indiana, five days a week (team onsite from 7:00am)
Competitive W2 hourly rate plus expenses
Commissioning and qualifying clean and black utilities, including WFI, potable and purified water, clean and plant steam, compressed air and process gases, CIP/SIP and cleanroom HVAC.
Carrying out P&ID walkdowns, loop checks, component verification and functional testing in the field.
Developing and executing IQ/OQ/PQ protocols in Kneat, and supporting FAT/SAT.
Working through punch lists, deviations and troubleshooting to keep systems moving.
Building turnover packages and traceability matrices for handover.
5+ years of hands-on C&Q experience in pharmaceutical or biotech GMP facilities.
Protocol development and execution experience, ideally in Kneat or a similar electronic validation system.
A good understanding of cGMP, ASTM E2500 and risk-based C&Q.
Greenfield or facility expansion experience is a strong plus. Exposure to DeltaV, SCADA or building automation is desirable.
A Bachelor’s degree in Engineering, Life Sciences or a related technical field.
Availability for overtime and occasional weekend work when the schedule requires it.
Details
| Company | i-Pharm GxP |
| Location | Lebanon, Indiana |
| Type | FULL TIME |
| Niche | Full-time |