On-Site Pharma CSV Engineer | Validation & Compliance
Listed on 2026-10-06
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Pharmaceutical
Pharma Engineer, Quality Engineering, Regulatory Compliance Specialist, Validation Engineer
Stallergenes Greer U.S. in Lenoir, NC is seeking a qualified professional to lead software validation projects within a highly regulated pharmaceutical environment.
Responsibilities include executing CSV assignments, developing master plans, protocols and summary reports, and coordinating with Validation, Engineering and QA to ensure compliant project delivery; engage end users for URS/FRS, and support continuous improvement of validation practices.
For the On-Site Pharma CSV Engineer | Validation & Compliance position at Stallergenes Greer U.S., we are reviewing applications now.
The On-Site Pharma CSV Engineer | Validation & Compliance role at Stallergenes Greer U.S. is now open for applications in Lenoir, NC, United States.
Join us at Stallergenes Greer U.S. as our next On-Site Pharma CSV Engineer | Validation & Compliance in Lenoir, NC, United States.
We are currently recruiting a On-Site Pharma CSV Engineer | Validation & Compliance for our team in Lenoir, NC, United States.
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