Validation Engineer (CSV/CQV)

Piper Companies is currently seeking an experienced Validation Engineer (CSV/CQV) in Raritan, NJ to work for an industry leading Pharmaceutical company.

Responsibilities for the Validation Engineer (CSV/CQV)

• Provide technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes while ensuring compliance with GMP and FDA standards.
• Conduct IQ, OQ, and PQ activities, as well as validate new laboratory equipment and methods.
• Support software updates and assist in creating SOPs, safety protocols, and work instructions.
• Oversee site validation master plans, ensure equipment and systems meet regulatory requirements, and drive continuous improvement initiatives.
• Collaborate with internal teams and external partners to communicate project progress effectively.

Qualifications for the Validation Engineer (CSV/CQV)

• 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.
• Skilled in reviewing and approving validation protocols and reports for facility/equipment commissioning, qualification, and change management.

Compensation for the Validation Engineer (CSV/CQV)

• Salary Range: $60-65/HR. 
• Long Term Contract
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 3/31/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Validation, CSV, CQV, IQ, OQ, PQ, Biomedical Engineering, Pharmaceutical, Biotechnology, Laboratory Equipment, Manufacturing Equipment, Equipment Validation, Equipment Commissioning, Validation Maintenance, Cleaning Validation,

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