Senior CQV Engineer – Onsite Cell Therapy Facilities

ZP Group; Raritan (NJ); On-site; USD 83,000 - 90,000; Part time

Job summary

Piper Companies is seeking a Senior CQV Engineer to support a leading cell therapy manufacturing organization in Raritan, NJ. This highly hands-on role requires expertise in commissioning, qualification, validation, remediation, and compliance within a cGMP environment, with the ability to manage multiple CQV projects and collaborate with Quality, Manufacturing, Engineering, and Validation teams.

The position is 100% onsite in Raritan, NJ and offers an initial 6-month contract with potential

Qualifications

• 8+ years of CQV experience in regulated pharma/biotech environments.
• Experience managing multiple CQV projects concurrently (3+ preferred).
• Experience with IQ/OQ/PQ protocols and validation lifecycle documentation.

Responsibilities

• Execute CQV activities for facilities, utilities, equipment, and manufacturing systems.
• Lead multiple CQV projects, ensuring timelines and compliance.
• Author, review, and approve CQV documents and risk assessments.
• Develop qualification strategies for cleanrooms, utilities, and process equipment.
• Support deviations, CAPAs, and remediation from a CQV perspective.
• Provide technical guidance and mentorship to CQV team members.

Skills

CQV

Project management

Regulatory compliance

Communication

On-site work

Education

Bachelor's degree in Engineering/Life Sciences

Tools

Maximo

Siemens EMS

Comet

Kneat

Kaye ValProbe

AVS

Job description

Piper Companies is seeking a Senior CQV Engineer to support a leading cell therapy manufacturing organization in Raritan, NJ. This highly hands-on role requires expertise in commissioning, qualification, validation, remediation, and compliance within a cGMP environment, with the ability to manage multiple CQV projects and collaborate with Quality, Manufacturing, Engineering, and Validation teams.

The position is 100% onsite in Raritan, NJ and offers an initial 6-month contract with potential