Process Engineer III
Core
Lead process engineering activities in product line including validation, equipment qualification, and troubleshooting to support manufacturing operations.
Role type
Senior IC process engineer (GMP regulated environment)
Builds
Manufacturing processes, equipment, and fixtures for medical devices, pharmaceuticals, or biologics
Domain
Life sciences (medical devices, pharmaceuticals, biologics)
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Process validation, Cleaning validation, Equipment qualification (IQ/OQ/PQ), Root cause analysis, Statistical process control (SPC), Engineering change management, New product integration, Hypothesis testing, Project execution
Preferred skills
GMP regulated environment experience, Post-graduate degree, Financial systems competency
Technologies
Data acquisition systems, Statistical analysis tools
Responsibilities
Lead process engineering activities including validation and equipment qualification; Support production troubleshooting and process optimization; Design and develop manufacturing equipment and processes; Execute engineering studies to test project hypotheses; Support new product integration and process validation.
Seniority
Senior, hands-on IC
