Manufacturing Engineering Technician

About MedTech

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

You will be responsible for:

• Conduct comprehensive non-conformance investigations within the non-conformance system, including NCR initiation, containment/bounding, product control and disposition, root-cause analysis, corrective action, and full documentation.
• Lead cross-functional kaizen events to identify root causes of nonconformance and ensure implementation of effective corrective and preventive actions.
• Apply failure-analysis tools (for example, 5M) to perform robust investigations, analyze trends and data, and recommend improvements to processes, equipment, and systems.
• Propose and drive process and system enhancements; prepare and revise procedures and protocols using the document change control system.
• Implement corrective actions and continuous process improvements to reduce defects and improve product quality and reliability.
• Develop and deliver training and education to manufacturing teams on corrective actions, process changes, and quality best practices.
• Support internal and external audits and inspections by preparing required documentation, responding to observations, and executing corrective actions.

Qualifications / Requirements

Required:

• Associate's or Bachelor's Degree in technical field (engineering, manufacturing, or related)
• 1 to 5 years of experience in regulated industry (medical, pharmaceutical, aerospace, etc.)

Preferred:

• Experience working in quality management system such as EtQ Reliance.
• Experience working in document management system such as PTC Windchill.