Validation Engineer; CQV - LCMS
Job in
Titusville, Mercer County, New Jersey, 08560, USA
Listed on 2026-06-03
Listing for:
ZP Group
Full Time
position Listed on 2026-06-03
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Biomedical Engineer, Quality Engineering
Job Description & How to Apply Below
Location: Titusville
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):
* Pay Rate: $60-65/hr.
* Type:
Long-Term Contract
* Comprehensive Benefits:
Medical, Dental, Vision, 401K, PTO, Sick Leave, and Holidays
Application Period:
Opens 5/6/2026 and remains open for at least 30 days.
/OQ/PQ, Validation, GMP, FDA, Analytical Equipment, Data Integrity
#LI-JM1 #LI-ONSITE
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