Analysis Skills, Biotech and Pharmaceutical, Calibration, Chemistry, Commissioning, Data Quality, Documentation, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Laboratory Equipment, Learning Content Management Systems (LCMS), Process Validation, Quality Assurance, Quality Control, Standard Operating Procedures (SOP)
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 6/29/2026 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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