Validation Engineer (CQV – LCMS)

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 11/17/2025 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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