United Pharma Technologies Inc
CQV Engineer
Location:
Glendale, CA (Onsite)
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.
Experience in temperature mapping.
Experience in laboratory equipment qualification.
Solid understanding of cGMP, FDA, and validation lifecycle concepts.
Seniority level Mid‑Senior level
Employment type Contract
Industries Pharmaceutical Manufacturing and Biotechnology Research
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Glendale, CA (Onsite)
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.
Experience in temperature mapping.
Experience in laboratory equipment qualification.
Solid understanding of cGMP, FDA, and validation lifecycle concepts.
Seniority level Mid‑Senior level
Employment type Contract
Industries Pharmaceutical Manufacturing and Biotechnology Research
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