Sr. Research Associate will design and execute design-of-experiments (DOEs) to optimize surface chemistry processes for in vitro diagnostic systems, transitioning formulations from R&D through pilot scale-up and manufacturing under GMP/FDA design control.… The role requires hands-on expertise in fluorescence imaging/spectroscopy, microfluidics, molecular biology techniques (nucleic acid extraction, PCR, amplification), and consumable characterization—including test method design, acceptance criteria definition, and root-cause analysis. The candidate will author technical documentation (protocols, batch records, DHF submissions), collaborate cross-functionally with assay development, reagent chemistry, device engineering, manufacturing, and quality/regulatory teams, and support FDA submissions (510(k)/PMA, CE-IVDR). Strong systematic troubleshooting, laboratory skills, and ability to present data to leadership are essential.
fda-design-controls jobs in San Diego
This Systems Engineer role at a medical device company requires decomposing regulatory and stakeholder requirements into testable system specifications, leading design reviews and verification/validation activities, and supporting risk management under FDA and ISO frameworks. The position demands 2+ years in a regulated medical device environment, with responsibility for traceability documentation, design history files, failure investigation, and CAPA activities.… Key competencies include FDA design controls, ISO 14971 risk management, human factors/usability per FDA guidance, and cross-functional communication of complex system interfaces to diverse audiences.
The Senior Design Quality Engineer ensures digital health products comply with FDA regulations, quality standards, and user requirements through design controls and verification/validation activities. They manage digital health projects from concept to production using phase-gate approaches, lead or support CAPAs and NCRs, conduct internal/external audits, and apply risk management throughout the design lifecycle.… The role requires advanced knowledge of FDA design controls and IEC 62304 software standards, with hands-on experience taking products through regulatory compliance. The engineer will work independently, provide executive guidance on quality matters, and serve as a best-practice resource within their area of expertise.