CQV Validation Engineer – Life Sciences

Pinnaql; United States; On-site; USD 110,000 - 140,000; Full time

Job summary

Pinnaql in the United States seeks an experienced Validation Engineer with CQV expertise to support life sciences projects. You will execute and document commissioning, qualification and validation activities for facilities, utilities, equipment and processes in compliance with GMP and regulatory standards.

Collaborate with Engineering, Quality, Manufacturing and Project Management to deliver audit-ready validation packages and support inspections.

Qualifications

• Candidates should have hands-on CQV experience and strong GMP knowledge.
• Experience developing or executing validation/qualification protocols in regulated environments.
• Ability to interpret engineering drawings and technical documentation.

Responsibilities

• Execute and support CQV activities for life sciences facilities and equipment.
• Develop and review validation documentation including plans, URS, risk assessments, IQ/OQ/PQ protocols.
• Track deliverables and ensure audit-ready documentation.

Skills

CQV experience

Validation

Technical writing

Project management

GMP knowledge

Education

Bachelor's degree in Engineering or Science

Tools

IQ/OQ/PQ protocols

Job description

Pinnaql in the United States seeks an experienced Validation Engineer with CQV expertise to support life sciences projects. You will execute and document commissioning, qualification and validation activities for facilities, utilities, equipment and processes in compliance with GMP and regulatory standards.

Collaborate with Engineering, Quality, Manufacturing and Project Management to deliver audit-ready validation packages and support inspections.