Validation Engineer (CQV - LCMS)

ZP Group • Titusville, NJ

79d • $60 - $65 • Onsite

About The Position

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.

Requirements

• 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.

Responsibilities

• 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.

Benefits

• Medical
• Dental
• Vision
• 401K
• PTO
• Sick Leave
• Holidays

What This Job Offers

• Career Level: Mid Level
• Industry: Professional, Scientific, and Technical Services
• Number of Employees: 251-500 employees