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Job description
Actalent seeks a Quality Engineer with at least 2 years of medical device manufacturing experience to support sustainability initiatives while ensuring FDA compliance. You will partner with Quality, Manufacturing, Engineering, Supply Chain, and Sustainability teams to drive environmentally responsible improvements.
Responsibilities include maintaining 21 CFR 820 compliance, risk assessments, CAPA investigations, supplier and internal audits, data analysis, and validation activities.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.