Manufacturing & Process Development Engineer

Why you should join

This is a rare opportunity to be part of something truly transformative. You won't just be joining another technical role—you’ll be contributing to the design, development, and transition to manufacturing of next-generation medical devices that have the potential to reshape the tech landscape and redefine the standards in healthcare.
We are part of a highly ambitious and global project, collaborating across multiple sites and stages.

Your main tasks

• Drive generation, implementation, qualification and optimization of fabrication processes for the fabrication of complex polymer consumables from prototype through high volume manufacturing with expertise and confidence of DFM.
• Develop, validate, and optimize manufacturing processes for new medical device products.
• Collaborate with cross-functional teams to ensure DFM principles are applied.
• Execute V&V protocols and prepare reports under ISO 13485.
• Conduct PFMEAs and risk assessments for new processes.
• Manage Engineering Change Orders (ECOs) and related documentation.
• Collaborate with cross-functional, global teams in an agile, startup-like environment.
• Help build and stabilize processes as part of a growing unit.

Your ideal background

• Bachelor’s in Engineering, Manufacturing, or related field.
• 3+ years in process development/manufacturing (Life Sciences or regulated industries preferred).
• ISO 13485 cleanroom experience (preferred).
• Experience scaling processes from R&D to manufacturing.
• Experience in one or more of the following processes is desirable: DRIE on silicon; Wet etching (silicon and glass); Sputtering and evaporation; Soft-lithography; Metrology; Photolithography for mold generation; Electroplating for nickel shims; Machining (e.g., CNC, micro-milling, laser welding); Injection molding.
• Proficiency in MS Office and 2D/3D CAD design tools. 
• Fluent in English; Spanish proficiency is a plus.

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Competencies