Fda Qsr Jobs

VahatiCor seeks a Process Development Engineer to lead catheter process development, transfer, and validation in its onsite Santa Clara manufacturing environment.

Experienced maintenance planner needed to lead CMMS-driven scheduling, optimize preventive maintenance, and coordinate cross-functional resources at a regulated medical device manufacturing site in Roseville, CA.

Plexus is hiring a Design Assurance Engineer intern in Neenah, WI to assist with medical device compliance, verification testing, and risk management activities for new product development.

PROCEPT BioRobotics is looking for a Senior NPI Manufacturing Engineer to lead design-for-excellence, process validation, and manufacturing transfer for new electromechanical medical devices.

Abbott's Lingo division is hiring a Quality Engineer II to lead design control, CAPA, and risk-management activities for medical devices and SaMD from our Alameda, CA site.

Lead the development and validation of automated and manual incoming inspection methods at PROCEPT BioRobotics to ensure high-quality components for medical device manufacturing.

Lead cross-functional continuous improvement for design quality at Insulet, implementing SDLC best practices and regulatory-aligned process improvements to accelerate compliant product development.

Abbott seeks a Senior Design Control Software Quality Engineer to validate and maintain Lingo product software and computerized quality systems in compliance with medical device regulations.

Senior quality executive needed to lead Irvine and global laboratory operations, standardize best-in-class systems, and ensure regulatory compliance across the organization.

Serve as Associate General Counsel, Senior Director of Regulatory Compliance & Privacy to lead Oura’s global regulatory, privacy, and corporate compliance programs for wearable and digital health products.