Process Engineering Support Technician
GE HealthCare · State College, PA · Yesterday
Information TechnologyFull-time
Essential Responsibilities
- Contribute technical expertise to manufacturing processes, tooling, fixtures, and equipment improvements.
- Support the release, qualification, implementation, and lifecycle management of manufacturing tooling and fixtures.
- Apply standardized methods and solutions across a variety of manufacturing processes.
- Create, revise, and maintain manufacturing procedures, work instructions, maintenance records, and technical documentation.
- Implement approved engineering changes affecting product design, tooling, processes, and documentation.
- Partner with Production, Quality, Purchasing, and Supply Chain teams to support troubleshooting, process improvements, supplier qualification, and project execution.
- Perform cross-sectioning, polishing, measurement, and analysis of product features, and communicate findings to Process Engineers.
- Support the evaluation and improvement of manufacturing methods to reduce lead time, increase reliability, and improve yield.
- Cook up preventive maintenance, calibration, troubleshooting, and repair activities for electro-mechanical manufacturing equipment, tooling, and fixtures.
- Maintain maintenance, calibration, tooling, inventory, and change-control records to ensure manufacturing readiness and minimize downtime.
- Prepare technical reports, project updates, maintenance summaries, and documentation packages for management review.
Required Qualifications
- A high school diploma or equivalent.
- Experience supporting manufacturing equipment, tooling, fixtures, and documentation systems.
- Experience with technical documentation, work instructions, engineering change processes, and document control systems.
- Mechanical and electrical troubleshooting experience.
- Ability to work in a cross-functional environment.
Preferred Qualifications
- An associate degree in a technical discipline.
- Experience implementing engineering changes and maintaining controlled manufacturing documents.
- Experience in an FDA-regulated, ISO 13485, or other highly regulated manufacturing environment.
- Ability to manage multiple priorities involving tooling maintenance, process support, and engineering change activities.
- Strong interpersonal, organizational, written, and verbal communication skills.
- Demonstrated commitment to continuous learning and technical development.
- Brought energy, accountability, and a continuous improvement mindset to daily activities.
Work Environment
General manufacturing environment with regular interaction with production equipment, tooling, laboratory equipment, and engineering development activities.