CQV Engineer: GMP Validation & Commissioning

Eurofins USA BioPharma Services; Lancaster (Lancaster County); On-site; USD 85,000 - 125,000; Full time

Benefits offered by this job

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services is seeking a CQV Engineer to lead commissioning, qualification and validation activities for pharmaceutical and biotech facilities. You will author IQ/OQ/PQ protocols, perform field verifications, and maintain full documentation in a GMP setting.

With 2+ years of GMP experience, you will read P&IDs and produce regulator-ready documents. The role requires on-site work in Lancaster, PA and occasional extended hours.

Qualifications

• Two or more years of hands‑on experience in a GMP‑regulated environment, with commissioning, qualification or validation activity.
• Ability to read and work from technical drawings, particularly P&IDs.
• Clear technical writing and documentation skills.

Responsibilities

• Author and execute IQ, OQ and PQ protocols for utilities, equipment and facilities.
• Perform field verifications and walkdowns against P&IDs and log discrepancies.
• Write deviation and summary reports and support investigations.

Skills

GMP experience

Technical writing

Field work

Education

Engineering degree or life science degree

Job description

Eurofins USA BioPharma Services is seeking a CQV Engineer to lead commissioning, qualification and validation activities for pharmaceutical and biotech facilities. You will author IQ/OQ/PQ protocols, perform field verifications, and maintain full documentation in a GMP setting.

With 2+ years of GMP experience, you will read P&IDs and produce regulator-ready documents. The role requires on-site work in Lancaster, PA and occasional extended hours.