Process Development Engineer

Lead and support design transfer activities to external manufacturing partners (CMOs), including product and engineering changes. Optimize and scale manufacturing and assembly processes for medical device consumables in collaboration with external manufacturing partners. Support process validation activities (IQ/OQ/PQ), equipment qualification, and manufacturing readiness. Identify and implement process and automation improvements to increase robustness, reduce manufacturing risks, and improve efficiency. Collaborate closely with suppliers and cross-functional teams including Quality, Operations, Supply Chain, and R&D.

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• Degree in Production Engineering, Mechanical Engineering, Medical Engineering, or similar technical field

• 5–10 years of experience in process development, industrialization, manufacturing engineering, or design transfer within MedTech, preferably in plastic part assembly and consumable manufacturing

• Knowledge of medical device production standards, sterilization processes and regulated manufacturing environments

• Independent and structured working style with strong ownership mindset

• Fluent in English; German and/or Spanish are considered a plus

• Willingness to travel internationally (30–40%)