What are the responsibilities and job description for the CQV Engineer position at Sterling Engineering?
Position: CQV Engineer (Pharma / Biotech)
Location: Chicago, IL
Duration: Long Term contract, on our team- This opportunity is NOT open for C2C or sponsorship at any time.
Pay rate $60.00 - $75.00 per hour
I am looking for a hands-on CQV Engineer to support a high-impact pharmaceutical manufacturing project. If you’ve led IQ/OQ/PQ, thrive in GMP environments, and enjoy being on the floor driving execution — this is worth a look. this is to join my Sterling Engineering team for multiple clients. NO C2C.
Overview Of Responsibilities
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.
Location: Chicago, IL
Duration: Long Term contract, on our team- This opportunity is NOT open for C2C or sponsorship at any time.
Pay rate $60.00 - $75.00 per hour
I am looking for a hands-on CQV Engineer to support a high-impact pharmaceutical manufacturing project. If you’ve led IQ/OQ/PQ, thrive in GMP environments, and enjoy being on the floor driving execution — this is worth a look. this is to join my Sterling Engineering team for multiple clients. NO C2C.
Overview Of Responsibilities
- Lead Commissioning, Qualification & Validation (CQV) activities
- Author & execute IQ / OQ / PQ protocols
- Perform hands-on equipment testing (functionality, alarms, interlocks, controls)
- Support FAT / SAT and system startup
- Partner with Engineering, Quality & Ops to drive systems to production readiness
- Own deviations, troubleshooting, and re-testing during validation
- Ensure all work meets cGMP & FDA compliance standards
- 5 years of CQV / Validation experience in pharma, biotech, or regulated manufacturing
- Strong experience with equipment, utilities, or facility validation
- Proven background writing & executing IQ/OQ/PQ
- Experience with on-site, field-based validation & testing
- Solid understanding of FDA / cGMP environments
- Experience with DeltaV, Rockwell, or PLC systems is desired
- Background with clean utilities (WFI, clean steam, etc.)
- Exposure to TrackWise, Kneat, or Veeva
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.
Salary : $60 - $75