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# Engineer II, MS&T

- **Company:** Catalent
- **Location:** Severn, MD, United States
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** MATLAB, Data Processing, JMP (Statistical Software)
- **Published:** August 11, 2026
- **Apply:** https://us.experteer.com/career/view-jobs/engineer-ii-ms-and-t-21077-harmans-md-usa-58896427

## About the Role

_ milestones and participate in meetings * Collect and trend process data for client and internal reviews * Train GMP Manufacturing staff on client processes * Evaluate equipment and disposable systems for client projects * Conduct facility fit assessments, process modeling, and Continued Process Verification statistical analysis Tasks * Bachelor in Chemical Engineering, Chemistry, Biology, Life Sciences or related field with 3-6 years in pharma/biotech, or Master in same fields with 2+ years * Knowledge of protein and virus manufacturing in a cGMP environment * Experience in cell/microbial culture, protein purification, and fill/finish * Experience with process modeling software such as SuperPro, JMP, MatLab, or Aspen is a plus * On-site manufacturing floor presence and cross-functional collaboration experience Key requirements * medical, dental, and vision benefits effective day one * tuition reimbursement * competitive paid time off and 8 holidays * on-site career development and
diverse, inclusive culture

## Description

Experteer Overview In this Engineer II, MS&T role you translate client and development input into cGMP processes and serve as a subject matter expert in biologic upstream and downstream operations. You will lead tech transfer and investigations in a fast-paced, cross-functional setting on the manufacturing floor. The position supports GMP manufacturing of viral vector-based therapies, contributing to clinical and commercial supply. You join a mission-driven team delivering advanced therapies to patients. Compensation / Benefits * Lead MS&T project activities and serve as subject matter expert for cell culture, purification, and fill & finish processes * Lead process and product investigations and author investigation reports * Manage technology transfer projects from Catalent Process Development and external clients into GMP manufacturing * Prepare technology transfer documents, Master Production Records, and SOPs for GMP projects * Coordinate with Program Management to meet project milestones and participate in meetings * Collect and trend process data for client and internal reviews * Train GMP Manufacturing staff on client processes * Evaluate equipment and disposable systems for client projects * Conduct facility fit assessments, process modeling, and Continued Process Verification statistical analysis Tasks * Bachelor in Chemical Engineering, Chemistry, Biology, Life Sciences or related field with 3-6 years in pharma/biotech, or Master in same fields with 2+ years * Knowledge of protein and virus manufacturing in a cGMP environment * Experience in cell/microbial culture, protein purification, and fill/finish * Experience with process modeling software such as SuperPro, JMP, MatLab, or Aspen is a plus * On-site manufacturing floor presence and cross-functional collaboration experience Key requirements * medical, dental, and vision benefits effective day one * tuition reimbursement * competitive paid time off and 8 holidays * on-site career development and diverse, inclusive culture


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