About this opportunity
United Pharma lists this CQV Project Engineer (GMP / Commissioning & Qualification) opportunity in piscataway, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Are you a driven validation professional looking to make an immediate impact on a major GMP facility expansion? A leading global pharmaceutical company is seeking a Validation Specialist to support critical qualification activities for manufacturing equipment, facilities, and utilities during a high-priority site startup.
Responsibilities
- Design, review, and execute FAT, IQ, OQ, and PQ protocols for GMP equipment, utilities, and facilities.
- Act with a project management mindset to schedule vendors, manage tight timelines, and track validation deliverables.
- Perform re-qualification activities and write detailed technical investigation reports for non-conformances.
- Partner closely with Maintenance, Engineering, Quality, and external vendors to ensure seamless installation and commissioning.
- Generate weekly and monthly validation progress reports to keep project schedules on track.
Qualifications
- Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related field.
- 2+ years of validation/qualification experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment.
- Strong working knowledge of GDP, FDA regulations, and risk-based validation principles.
- Proven ability to draft/execute protocols, analyze test data, document discrepancies, and manage vendor schedules.
- Flexibility to work occasional weekend hours as required by project and vendor schedules.
skills: Good Manufacturing Practices (GMP), Equipment Validation
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.