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.
Keywords: CQV, LCMS, Mass Spec, IQ/OQ/PQ, Validation, GMP, FDA, Analytical Equipment, Data Integrity
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