Position: CQV Engineer
Location: Phoenix, AZ and Lincoln, NE Onsite
Project Overview:
Our client recently acquired an existing facility and is converting the building into a CDMO manufacturing site. The facility is currently in the shell stage and will require installation, commissioning, and qualification of new equipment and systems.
Key Responsibilities:
- Support C&Q activities for utilities, facility systems, and manufacturing equipment.
- Develop, review, and execute basic commissioning and qualification documentation.
- Perform field execution, equipment verification, walkdowns, and qualification activities.
- Identify, document, and support resolution of deviations and discrepancies.
- Work closely with construction, engineering, vendors, and project teams during installation and startup.
- Troubleshoot issues and provide practical, hands-on solutions throughout the C&Q lifecycle.
Ideal Candidate:
- Hands-on C&Q/Commissioning & Qualification experience in pharmaceutical, biotech, or CDMO environments.
- Strong experience with facility, utility, and equipment qualification.
- Comfortable writing and executing qualification/commissioning documents.
- Experience managing deviations and resolving field issues.
- Strong problem-solving skills with a hands-on "doer" approach.
- Ability to work onsite in the Phoenix, AZ area.
Regards
Hemasundar A
hemasundar.a@unitedpharmatechnologies.com