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