S & V Tek Systems LLC is a leading provider of business and technology services, focused on advancing clients’ transformation initiatives. The role covers leading process validations for single-use medical devices, developing validation protocols, and supporting audit readiness and remediation efforts.
You will apply Lean Six Sigma techniques to optimize validation workflows, support CQV activities for warehouse spaces, and contribute to regulatory review-ready documentation.
#J-18808-LjbffrValidation Engineer – Medical Devices & CQV Specialist in northern at Unknown Company
This position is listed as full time and onsite.