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Job summary
A leading healthcare company is seeking a Senior Validation Engineer to provide onsite support for Commissioning, Qualification, and Validation (CQV) and Equipment Validation activities in Wisconsin. The ideal candidate will have 8-10 years of experience in Validation Engineering, with a strong background in medical device manufacturing. Responsibilities include leading CQV activities, performing IQ, OQ, and PQ processes, and developing validation documentation. This role presents an exciting opportunity to enhance quality processes in a dynamic environment.
Qualifications
8–10 years of experience in Validation Engineering.
Strong hands-on experience with IQ/OQ/PQ validation.
Proven ability to write and execute validation documentation.
Experience with risk assessment methodologies and optimization activities.
Background supporting CDMO and medical device manufacturing environments.
Responsibilities
Lead and execute CQV and Equipment Validation activities.
Perform IQ, OQ, and PQ for manufacturing equipment.
Develop, execute, and author validation protocols, reports, and SOPs.
Conduct risk assessments and support process optimization.
Perform API functional testing as part of equipment and process validation.
Skills
Validation Engineering
Equipment Validation
Risk Assessment Methodologies
Process Optimization
Tools
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Job description
A leading healthcare company is seeking a Senior Validation Engineer to provide onsite support for Commissioning, Qualification, and Validation (CQV) and Equipment Validation activities in Wisconsin. The ideal candidate will have 8-10 years of experience in Validation Engineering, with a strong background in medical device manufacturing. Responsibilities include leading CQV activities, performing IQ, OQ, and PQ processes, and developing validation documentation. This role presents an exciting opportunity to enhance quality processes in a dynamic environment.