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 3/10/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.