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GE HealthCare Production Associate United States, Pennsylvania, State College 301784254
Yesterday
Key Responsibilities:
- Lead cross-functional efforts to transfer manufacturing processes and products between sites.
- Develop and execute validation plans, process documentation, and training materials.
- Collaborate with design, quality, planning, purchasing and operations teams to ensure compliance with regulatory standards.
- Leverage data to identify and implement process improvements to enhance efficiency and product quality.
- Serve as a technical liaison between various teams, providing hands-on support and troubleshooting.
- Lead root cause analysis and implement corrective and preventive actions (CAPA) for process-related issues.
- Monitor key process metrics and drive improvements in yield, cycle time, and cost.
- Travel domestically and internationally to support transfer activities and build strong site relationships.
Qualifications:
- Bachelor’s degree in an Engineering discipline from an accredited university (Mechanical, Electrical, Industrial, or related).
- Minimum of 5 years of experience in manufacturing or a regulated industry (e.g., medical devices, aerospace, automotive).
- Proven ability to communicate effectively across technical and non-technical audiences.
- Demonstrated self-motivation and ability to work independently with minimal supervision.
- Strong problem-solving skills and attention to detail.
- Interest in professional development and future leadership opportunities.
- Must possess a valid Passport
Preferred Qualifications:
- Experience with medical device manufacturing or ultrasound technology.
- Familiarity with regulatory standards such as ISO and FDA.
- Project management experience in cross-site or international environments.
- Familiarity with ERP and MES systems.
- Experience with Solidworks or equivalent design software.
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