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, 401

K, PTO, Sick Leave, and Holidays Application Period :

Opens 3/31/2026 and remains open for at least 30 days.

Keywords :

CQV, LCMS, Mass Spec, IQ/OQ/PQ, Validation, GMP, FDA, Analytical Equipment, Data Integrity #LI-JM1 #LI-ONSITE