Senior Quality Engineer - Hybrid Pharma QA & Validation

A biopharmaceutical company in Northbridge, MA, is seeking a Quality Engineer to oversee drug product validation and qualifications. The role involves ensuring compliance with regulatory standards and maintaining inspection readiness. Candidates should have 3-7 years of cGMP experience, with a strong background in the pharmaceutical industry and effective communication skills. This position offers a hybrid work schedule, contributing to a culture that emphasizes innovation and operational excellence.
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