CQV Specialist

Piper Companies; Titusville (NJ); On-site; USD 83,000 - 96,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

Retirement plans

Job summary

Piper Companies is seeking a CQV Specialist in Titusville, NJ to lead commissioning and qualification activities for QC lab equipment, with focus on TCU systems. The role ensures equipment is installed and validated to GMP and FDA standards, supporting lifecycle management and software validations.

The contract position offers an hourly pay rate of $60–$70, comprehensive benefits, and a 12-month assignment to support a leading pharmaceutical organization onsite.

Qualifications

• Experience supporting CQV/validation activities in GMP-regulated pharma/biotech environments.
• Hands-on in commissioning, IQ/OQ/PQ, and equipment qualification.
• Strong knowledge of FDA regulations and data integrity principles.

Responsibilities

• Lead commissioning and qualification activities for new QC lab equipment (TCU focus).
• Develop, execute, and document IQ/OQ/PQ protocols to meet regulatory and quality requirements.
• Perform method qualification and validation on lab instrumentation; support validation lifecycle docs.
• Coordinate decommissioning of legacy lab equipment with proper documentation and asset retirement.

Skills

CQV experience

Validation

GMP compliance

FDA regulations

Data integrity

Laboratory systems

Job description

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.

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