<p>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.</p> <p>Responsibilities for the Validation Engineer (CQV - LCMS):</p> <ul> <li>Execute IQ/OQ/PQ for LCMS and other analytical instruments. </li><li>Develop and maintain CQV documentation (URS, protocols, reports). </li><li>Ensure equipment qualification and data integrity meet GMP/FDA standards. </li><li>Support equipment installation, lifecycle management, and periodic reviews. </li><li>Draft and update SOPs, calibration procedures, and work instructions. </li><li>Collaborate with QC, QA, Engineering, and vendors on equipment readiness. </li></ul> <p>Qualifications for the Validation Engineer (CQV - LCMS):</p> <ul> <li>Bachelor's degree in chemistry, Engineering, or related field. </li><li>3+ years of pharmaceutical/biotechnology experience. </li><li>Hands-on experience with LCMS qualification or validation. </li><li>Strong knowledge of CQV, GMP, and IQ/OQ/PQ requirements. </li><li>Skilled in writing and reviewing SOPs, protocols, and qualification reports. </li></ul> <p>Compensation for the Validation Engineer (CQV - LCMS):</p> <ul> <li>Pay Rate: $60-65/hr. </li><li>Type: Long-Term Contract </li><li>Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave, and Holidays </li></ul> <p>Application Period: Opens 12/9/2025 and remains open for at least 30 days.</p> <p>Keywords: CQV, LCMS, Mass Spec, IQ/OQ/PQ, Validation, GMP, FDA, Analytical Equipment, Data Integrity</p> <p>#LI-JM1 #LI-ONSITE</p>