Senior Manufacturing Engineer - Onsite
Medtronic
Medtronic seeks a Senior Manufacturing Engineer to develop and optimize manufacturing processes for ENT surgical devices in a regulated environment. The role encompasses process validation, equipment qualification, continuous improvement, and regulatory compliance, based in Jacksonville, Florida with 4 days/week onsite.
Responsibilities
- Design, develop, and optimize manufacturing processes, equipment, and workflow layouts for safety and efficiency
- Lead process validation, equipment qualification, and manufacturing readiness for product changes
- Analyze manufacturing performance data and implement corrective and preventive actions
- Develop and maintain manufacturing documentation including work instructions and SOPs
- Partner with Quality, Operations, and R&D on product transfers, design changes, and continuous improvement
Requirements
- Bachelor's degree with 4+ years manufacturing engineering experience, or Master's with 2+ years, or PhD
- Experience developing and sustaining manufacturing processes in regulated production environments
- Experience with process validation, equipment qualification, or manufacturing process development
- Experience analyzing process performance data and implementing corrective actions
- Preferred: statistical process control and process capability analysis experience
- Preferred: medical device manufacturing background
- Preferred: Lean Manufacturing and continuous improvement methodology experience
Vacancy posted 1 day ago
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