The Assistant Process Engineer 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 preparation of technical documentation such as validation protocols, reports, and summaries. The position collaborates with Manufacturing Science and Technology (MS&T) teams and helps ensure cGMP compliance and inspection readiness. This is a six-month W-2 contract with a possible extension of 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. The client retains the right to hire the contractor directly.
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Job Type
Full-time
Career Level
Entry Level