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Validation Engineer (CQV LCMS)
Job
Piper Companies
Hopewell Township, NJ (In Person)
$130,000 Salary, Full-Time
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Job Description
Piper Companies is seeking a Validation Engineer (CQV - LCMS) in Titusville, NJ to support an industry-leading pharmaceutical organization. This role focuses on commissioning, qualification, and validation of LCMS and analytical laboratory equipment in a GMP environment. Responsibilities for the Validation Engineer (CQV - LCMS):
- Execute
IQ/OQ/PQ
for LCMS and other analytical instruments.- Develop and maintain CQV documentation (URS, protocols, reports).
- Ensure equipment qualification and data integrity meet GMP/FDA standards.
- Support equipment installation, lifecycle management, and periodic reviews.
- Draft and update SOPs, calibration procedures, and work instructions.
- Collaborate with QC, QA, Engineering, and vendors on equipment readiness. Qualifications for the Validation Engineer (CQV - LCMS):
- Bachelor's degree in chemistry, Engineering, or related field.
- 3+ years of pharmaceutical/biotechnology experience.
- Hands-on experience with LCMS qualification or validation.
- Strong knowledge of CQV, GMP, and
IQ/OQ/PQ
requirements.- Skilled in writing and reviewing SOPs, protocols, and qualification reports. Compensation for the Validation Engineer (CQV - LCMS):