Equipment Commissioning Manager
2 weeks ago
Piper Companies is currently seeking an experienced Validation Engineer (CSV/CQV) to work in Raritan, NJ. The ideal candidate will provide technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes while ensuring compliance with GMP and FDA standards.
Responsibilities
The Validation Engineer (CSV/CQV) will be responsible for:
- Providing technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes.
- Conducting IQ, OQ, and PQ activities, as well as validating new laboratory equipment and methods.
- Supporting software updates and assisting in creating SOPs, safety protocols, and work instructions.
- Overseeing site validation master plans, ensuring equipment and systems meet regulatory requirements, and driving continuous improvement initiatives.
Requirements
- Bachelor's degree in Chemical Engineering, Biomedical Engineering, or a related field.
- Over 3 years of experience in biotechnology and/or pharmaceutical industries.
- Proficient in drafting SOPs, validation reports, and work instructions.
- Skill in reviewing and approving validation protocols and reports for facility/equipment commissioning, qualification, and change management.
Compensation and Benefits
- Salary Range: $60-65/HR.
- Long Term Contract.
- Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays.
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