We are seeking an MS&T Process Validation Specialist to support process validation activities at a cell therapy manufacturing facility in Devens, MA.
This role focuses on supporting aseptic process simulations and validations (APS/APV), process lifecycle management changes, and the preparation of technical documentation, including validation protocols, reports, and summaries.
Key responsibilities:
Support process validation activities, including aseptic process simulations and validations;
Prepare technical protocols, validation reports, and study summaries;
Support implementation of process lifecycle management changes;
Ensure compliance with cGMP requirements and maintain inspection readiness;
Collaborate with Manufacturing Science and Technology (MS&T) teams to support validation activities.
Position details:
Hourly rate: $31.40–$34.40;
Contract length: 6 months with possible extension up to 2 years;
Location: Devens, MA 01434;
Work arrangement: Hybrid, 50% onsite;
Schedule: Monday–Friday, normal business hours;
Maximum hours: 40 hours per week;
W-2 contract position;
No C2C options;
No visa sponsorship.
Requirements
Required:
Bachelor's degree in Science, Engineering, Biochemistry, or a related discipline;
Minimum 2 years of experience in biopharmaceutical operations or equivalent;