Fda Qsr Jobs

Multiply Labs seeks a Head of Supply Chain to build and scale a global supply chain for robotic cell-therapy manufacturing systems and consumables.

Lead first-shift assembly operations and a team of ~50 production employees at Medtronic’s Plymouth facility to deliver safe, compliant, and efficient manufacturing for Peripheral Vascular Health products.

Medtronic is hiring a Design Quality Engineer II to provide design-control and risk-management engineering support for ACM medical device products, ensuring compliance with ISO13485, FDA QSR and related standards.

Lead and scale post-commercialization technical support, field service, and customer experience for Nautilus's proteomic analysis platform based in San Carlos, CA.

Medtronic is hiring a Quality Systems Manager in Northridge to lead standards compliance, quality engineering, and data-driven improvements across Mini‑Med manufacturing.

Selution (partnered with Cordis) is hiring a Manufacturing Engineer II to lead process development, validation, and troubleshooting for Class IIb/III implantable devices in an onsite cleanroom manufacturing setting.

FUJIFILM Irvine Scientific is hiring a QA In-Process Inspection Lead to oversee real-time manufacturing inspections and ensure GMP compliance on the overnight shift.

Philips is hiring a Mechanical R&D Development Engineer to drive design changes, create CAD and design documentation, prototype components, and support medical device development and sustaining activities.

Field-based sales professional needed to grow CoolSculpting and body-contouring consumable adoption across plastic surgery and dermatology practices in the North Central region through training, account management, and targeted marketing support.

Sentec is hiring a Global Complaint Resolution Manager to lead complaint handling, manage FSCA/recalls, and ensure regulatory compliance for high‑risk medical devices.

Penumbra is hiring a Production Supervisor for the swing shift in Roseville, CA to lead manufacturing operations, enforce QMS compliance, and drive lean production improvements.

Penumbra is hiring an on-site Production Supervisor in Roseville, CA to lead production lines, enforce SOPs, and drive lean improvements in a regulated medical device manufacturing environment.

Intuitive Surgical is looking for a hands-on Mechanical Design Engineer to design electromechanical systems and prototypes that support next-generation robotic-assisted surgical platforms.

Nemera seeks a Quality Validation Engineer to lead validation projects, supplier quality activities and investigations to maintain regulatory and ISO compliance at its Buffalo Grove medical device manufacturing site.

A seasoned Quality Engineer role focused on leading design control, risk management, and verification/validation efforts for electromechanical and software-driven surgical systems at Intuitive Surgical.

StemWave seeks a Senior Firmware Engineer in Woburn to lead embedded firmware development for Class II medical devices, driving regulatory-compliant design and validation.