MiniMed is seeking a Principal Quality Engineer - Process Development to lead validation and process development across multiple product platforms. The role requires ensuring SOP adherence while driving cross-functional alignment and rapid issue resolution.
You will author Master Validation documents, apply DRM/DFSS/DFMA, and manage pFMEA to mitigate process risks in NPI and scale-up. Strong collaboration with R&D and supplier quality is essential.
#J-18808-LjbffrPrincipal Quality Engineer – Medical Devices, Process in los angeles at Unknown Company
This position is listed as full time and onsite.