EyePoint is seeking a Senior Quality Engineer (Drug Product Development) to join their team in Northbridge, MA. The role involves overseeing quality engineering for drug product validation and associated qualifications.
About the Role
As a Senior Quality Engineer, you will be responsible for quality oversight of drug product process development, ensuring compliance with regulatory requirements, and collaborating with various departments to maintain inspection readiness. Your daily tasks will include reviewing validation activities, conducting risk assessments, and supporting continuous improvement initiatives.
About You
Required:
Bachelor of Science in a relevant field (Science/Engineering).
3 - 7 years of cGMP experience in drug product process validation and Quality Engineering roles.
Preferred:
Extensive experience in the pharmaceutical industry with drug product processes.
ASQ (American Society for Quality) and/or ISO certification as a Certified Quality Engineer.
Benefits
Hybrid work schedule.
Robust total rewards in a science-based entrepreneurial culture.
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