Lead Validation Engineer - GMP CQV Expert (Onsite)
Sterling Engineering
A leading engineering firm is seeking a Lead Validation Specialist to support commissioning and validation initiatives. This hands-on role involves executing validation strategies and mentoring junior specialists. Candidates should have a strong background in FDA regulations and experience in the regulated industry. Responsibilities include leading validation activities, managing projects, and maintaining compliance. Ideal for those with a Bachelor's degree in Engineering or similar and 5-10 years of relevant experience. This is a full-time position requiring on-site presence in Mundelein, IL. #J-18808-Ljbffr Sterling Engineering
Vacancy posted 1 day ago
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