Senior Specialist, Associate Aseptic Process Validation Engineer

What you’d do

Support execution of aseptic process simulations and validations, author qualification and validation documents, lead aseptic risk assessments, and own site change controls. Full time role in Devens, MA, maintaining cGMP compliance and inspection readiness. Found on the employer's careers page on Oct 7, 2026. Apply through the link.

You’ll need

• Experience in cGMP and biopharmaceutical/cell therapy regulations
• Experience in aseptic processing/validation and clean room design
• Experience with internal and health authority audits
• Excellent verbal/written communication skills