What are the responsibilities and job description for the CQV engineer position at United Pharma Technologies Inc?
Job Title: CQV Engineer
Location: Glendale, CA (Onsite)
Job Description
We are seeking an experienced CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and/or biotech facilities in Glendale, CA. The ideal candidate will have hands-on experience with autoclaves, HVAC/AHU systems, clean utilities, laboratory equipment, and temperature mapping, ensuring compliance with cGMP and regulatory requirements.
Key Responsibilities
- Execute Commissioning & Qualification (C&Q) activities for GMP systems and equipment.
- Perform Component & System Qualification (CNQ / CQV) including IQ, OQ, and PQ protocols.
- Support qualification of autoclaves, AHU/HVAC systems, and cleanroom utilities.
- Conduct and support temperature and humidity mapping studies for controlled environments, warehouses, cold rooms, incubators, and stability chambers.
- Qualify laboratory equipment such as balances, ovens, incubators, refrigerators, freezers, and biosafety cabinets.
Required Qualifications
- Bachelor’s degree in Engineering, Life Sciences, or related field.
- 3–8 years of experience in CQV within pharmaceutical, biotech, or medical device environments.
- Temperature Mapping
- Laboratory Equipment Qualification
- Solid understanding of cGMP, FDA, and validation lifecycle concepts.