Senior CQV Engineer — GMP Validation & Commissioning

Adryan; Iowa (LA); On-site; USD 95,000 - 135,000; Full time

Benefits offered by this job

Company car

Laptop

Phone

Personal training budget

Job summary

Adryan is seeking a hands-on commissioning, qualification and validation (CQV) engineer for life sciences projects in the United States. You will manage CQV activities for GMP facilities, equipment, and utilities, ensuring compliance with FDA/EU guidelines and quality standards.

You will design, execute, and document IQ/OQ/PQ processes and generate final reports. Required: Bachelor’s in engineering or related field, 5+ years GMP, 3+ years CQV, and strong teamwork, communication, and

Qualifications

• Bachelor’s degree in engineering or related technical field is required.
• 5+ years of experience in a GMP environment, preferably biotech.
• 3+ years of CQV experience is required.
• Solid understanding of controlled documentation and data systems.
• Strong communication and collaboration skills.

Responsibilities

• Lead CQV activities per project timelines and budgets.
• Develop and execute IQ/OQ/PQ protocols and reports.
• Analyze validation data and summarize findings in final reports.
• Identify GMP requirements in design and validation activities.
• Coordinate validation testing and resolve discrepancies.
• Maintain proactive teamwork and knowledge sharing.

Skills

GMP knowledge

CQV experience

Team player

Communication skills

Problem solving

Adaptability

Education

Bachelor’s degree in engineering or related field

Tools

MS Office

Document control systems

Job description

Adryan is seeking a hands-on commissioning, qualification and validation (CQV) engineer for life sciences projects in the United States. You will manage CQV activities for GMP facilities, equipment, and utilities, ensuring compliance with FDA/EU guidelines and quality standards.

You will design, execute, and document IQ/OQ/PQ processes and generate final reports. Required: Bachelor’s in engineering or related field, 5+ years GMP, 3+ years CQV, and strong teamwork, communication, and