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- Ensure that new, state of the art systems have a quality design and acceptable installation plans
- Support commissioning and qualification of equipment and clean utilities in collaboration with construction and project controls
- Document evidence to summarize validation and ensure equipment performance delivers consistent results
- Troubleshoot for inconsistencies found from validation
- Support the design and review of automation systems (PLC and Delta-V)
- Qualify new projects and lead ongoing improvements by acting as a client agent. Build strong external and internal relationships that facilitate quality outcomes that meet essential project deadlines.
- B.S. or M.S. in an Engineering discipline, or a related field
- 10+ years of experience in a biotechnology or pharmaceutical manufacturing environment
- Understanding of construction partnerships and equipment contracts
- $90 - $105/hr., depending on years of relevant experience
- Medical, Dental, Vision, 401k, PTO
Senior CQV Engineer - Raleigh, United States - ZP Group
Description
Piper Life Sciences is seeking a Senior CQV Engineer for a growing pharmaceutical manufacturing site in Holly Springs, North Carolina. The Senior CQV Engineer will play an integral role in the review and approval of utilties and equipment designs. The ideal candidate will have experience with new or expanding manufacturing facility projects.
Responsibilities for the Senior CQV Engineer
Qualifications for the Senior CQV Engineer
Compensation for the Senior CQV Engineer
Keywords: CQV, commissioning, qualification, validation, equipment upgrade, automation, process improvement, engineering, pharmaceutical, chronic diseases, pharmaceutical, Raleigh, North Carolina