Find & Apply For Validation Engineer Jobs in Hopewell Township, New Jersey

Piper Companies is seeking a CQV Specialist to support the commissioning, qualification, validation, and lifecycle management of lab equipment for a leading pharmaceutical organization in Titusville, NJ . The CQV Specialist will play a key role in ensuring lab systems are installed, qualified, and maintained in compliance with GMP, FDA, and industry regulatory requirements while supporting organization initiatives. Responsibilities of the

CQV Specialist:

• Lead commissioning and qualification activities for new QC lab equipment, with a primary focus on TCU equipment and associated lab systems.
• Develop, execute, and document

IQ/OQ/PQ

protocols to ensure equipment meets regulatory, quality, and operational requirements.

• Perform method qualification and validation activities on newly installed lab instrumentation and support validation lifecycle documentation.
• Support lab software upgrades and change control activities while maintaining equipment in a validated state.
• Coordinate decommissioning activities for legacy lab equipment, ensuring proper documentation, compliance, and asset retirement processes.

Qualifications of the

CQV Specialist:

• 5+ years of experience supporting CQV, validation, or qualification activities within a GMP-regulated pharmaceutical or biotechnology environment.
• Hands-on experience developing and executing commissioning, IQ/OQ/PQ, and equipment qualification protocols.
• Strong understanding of FDA regulations, GMP requirements, data integrity principles, and validation lifecycle practices.
• Experience supporting lab instrumentation, analytical equipment, computerized systems, and software validation activities. Compensation for the CQV Specialist includes:
• Pay rate: $60-$70/hour depending on experience
• Comprehensive benefits package including medical, dental, vision, and retirement plans
• 12 month contract position This job opens for applications on 10/27/2026.

Applications for this job will be accepted for at least 30 days from the posting date. SEO Keywords CQV Specialist, Commissioning Qualification Validation, CQV Engineer, Validation Specialist, Equipment Qualification, IQ

OQ PQ, GMP

Compliance, FDA Regulations, Laboratory Validation, QC Laboratory Equipment, TCU Equipment, Method Validation, Method Qualification, Computer System Validation, CSV, Laboratory Software Validation, Pharmaceutical Validation, Biotechnology Validation, Commissioning Engineer, Qualification Engineer, Analytical Instrument Validation, SOP Development, Change Control, Regulatory Compliance, Lifecycle Management, Laboratory Systems #LI-OG1 #LI-ONSITE