A leading biopharmaceutical company is seeking a CQV Engineer to support the Commissioning, Qualification, and Validation of equipment at its facility. This role is a 12-month contract with the possibility of extension.
Interviews and offer can happen this week so get in touch ASAP to discuss further!
Contract Details
* Contract Duration: 12 months (with possibility of extension).
* Work Hours: 40 hours per week.
* Start Date: ASAP
Key Responsibilities
* Lead commissioning, qualification, and validation (CQV) activities for new and existing equipment.
* Develop, execute, and report on validation protocols (IQ, OQ, PQ).
* Review and approve vendor protocols to ensure compliance with project requirements.
* Support troubleshooting, deviations, and change control related to equipment validation.
* Work closely with cross-functional teams to ensure seamless project execution.
Candidate Requirements
* Minimum 3 years of experience in a CQV role within the biopharmaceutical industry.
* Strong background in equipment commissioning and validation.
* Experience with utilities is a plus.
* Excellent documentation and communication skills.
Interested? Send your CV to r.tartaglione@panda-int.com to discuss further!
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