Validation Engineer (CQV – LCMS)
Piper Companies · Titusville, NJ · 2 days ago
On-siteQuality Assurance$60–$65/hrFull-time
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.
Qualifications
- 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.
Pay
Pay Rate: $60–65/hr.
Benefits
- Medical
- Dental
- Vision
- 401K
- PTO
- Sick Leave
- Holidays