CQV Specialist: Lab Equipment Validation Lead

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 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.