Senior QA Validation Lead – Sterile Fill-Finish

Mann Kind Corporation is seeking a QA Validation Manager to oversee the validation activities supporting sterile drug product manufacturing in Danbury, Connecticut. The candidate will manage validation strategies and teams, ensuring compliance with regulatory standards. Requirements include a bachelor's or master's degree in engineering or Life Sciences, with at least 8 years of QA experience in GMP environments. Candidates should possess strong skills in aseptic processing and contamination control, and be effective communicators.

This role is essential for maintaining high-quality operations.
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