More jobs:
Validation Engineer; CQV – LCMS
Job in
Titusville, Mercer County, New Jersey, 08560, USA
Listed on 2025-12-20
Listing for:
Piper Companies
Full Time
position Listed on 2025-12-20
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer
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.
- 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.
- Pay Rate: $60–65/hr.
- Type:
Long‑Term Contract - Comprehensive Benefits:
Medical, Dental, Vision, 401K, PTO, Sick Leave, and Holidays
Opens 11/17/2025 and remains open for at least 30 days.
/OQ/PQ, Validation, GMP, FDA, Analytical Equipment, Data Integrity
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