The MS&T Process Validation Specialist supports process validation activities at a cell therapy manufacturing facility in Devens, Massachusetts. The role focuses on aseptic process simulations and validations (APS/APV), process lifecycle management changes, and preparing technical documentation, including validation protocols, reports, and summaries. The specialist works with Manufacturing Science and Technology (MS&T) teams to support validation activities, ensure cGMP compliance, and maintain inspection readiness. This is a W-2 contract position with an initial six-month term and possible extension up to two years. The work arrangement is hybrid, with 50% onsite, and the schedule is Monday through Friday during normal business hours, up to 40 hours per week. The hourly rate is $31.40–$34.40. No C2C options or visa sponsorship are available.
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Career Level
Mid Level