Senior Quality Engineer: Drug Product Validation Lead

A leading ophthalmology company in Northbridge, MA, seeks a mid-senior level Quality Engineer to provide oversight of drug product validation and qualification. Candidates should have 3–7 years of cGMP experience, preferably within the pharmaceutical industry. The role includes ensuring compliance with regulatory requirements, collaborating with internal teams, and applying quality principles to improve processes. The position offers a competitive salary, ranging from $94,760 to $157,590 per year, in a full-time capacity.
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