TSMS Engineer

The TSMS Technical Transfer Engineer supports the successful transfer, scale-up, and lifecycle management of clinical and commercial manufacturing processes in a cGMP environment. This role partners closely with Operations, Validation, Quality, and external customers to ensure manufacturing processes are robust, well-documented, and capable of reliable commercial execution.

The Technical Transfer Engineer provides hands-on technical support across tech transfer, process validation, GMP floor support, and continued process verification, serving as a key technical resource throughout the manufacturing lifecycle.

Responsibilities Lead and execute technical transfer activities, including process scale-up from development or client-provided data into full-scale GMP manufacturing

Select appropriate manufacturing equipment and single-use components, and develop comprehensive technical documentation such as Tech Transfer Plans, Gap Assessments, Process Flow Diagrams, Summary Reports, and Process FMEAs

Serve as a TSMS representative on cross-functional project teams and act as a technical point of contact for customers

Author and review GMP manufacturing documentation, including Master Batch Records, Bills of Materials, and processing forms

Monitor and analyze process data, identify trends, and recommend actions to maintain process control and performance

Lead technical troubleshooting and investigations, including root cause analysis, product impact assessments, and CAPA development

Provide technical guidance and oversight to Operations and Validation teams during Process Performance Qualification (PPQ) and Continued Process Verification (CPV)

Collaborate cross-functionally to assess, implement, and support new technologies within GMP manufacturing

Evaluate and assess the impact of changes to product, process, equipment, materials, and procedures

Manage timelines and prioritize critical tasks to support on-time project execution

Perform additional duties as required to support manufacturing and project objectives

Qualifications Bachelor’s degree in Science or Engineering

Master’s degree in Science or Engineering (preferred)

2–3 years of experience in a pharmaceutical manufacturing environment

Experience supporting technical transfer within pharmaceutical, biotech, or related regulated industries in a client-facing role

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