CQV Engineer

Piper Companies is seeking a CQV Engineer to join a pharmaceutical company located in Titusville, NJ through a 12-month, onsite contract. The CQV Engineer will focus primarily on commissioning new quality control laboratory equipment.

Responsibilities of the CQV Engineer include:

• Commission and bring new QC laboratory equipment into service in compliance with GMP and FDA requirements
• Execute full equipment validation activities, including IQ, OQ, and PQ, as well as qualification of new analytical methods
• Support laboratory software upgrades and ensure systems remain validated and compliant
• Manage the decommissioning and retirement of obsolete QC laboratory equipment
• Develop and support SOPs and work instructions, while maintaining clear communication with internal stakeholders and external partners throughout the project lifecycle

Qualifications for the CQV Engineer include:

• Bachelor’s or master’s degree in engineering, biotechnology, or a related field is preferred
• Experience with Good Manufacturing Processes (GMP) is required
• Experience with Quality Control Lab Equipment Commissioning/Decommissioning is required

Compensation for the CQV Engineer includes:

• Pay Rate: $60-$70/hour
• Available Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 01/28/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: CQV, CQV engineer, engineer, pharmaceutical, healthcare, onsite, temporary, contract, quality control, laboratory, laboratory equipment, QC, GMP, lab equipment commissioning, lab equipment decommissioning, engineering, chemical engineering, biomedical engineering, pharmaceutical sciences, life sciences, biotechnology, IQ, OQ, PQ, analytical methods, SOPs        

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