jmp jobs in San Diego

Sr QA Engineer leading complex quality investigations, root cause analysis, CAPAs, and NCMRs at a regulated medical device company (Dexcom). Drives Quality Management System excellence through continuous improvement methodologies (Six Sigma, Lean, process capability analysis), owns validation and qualification strategies for equipment/processes/software, and guides design transfer and commercialization from development to high-volume manufacturing.…See more Requires advanced quality engineering knowledge, hands-on technical aptitude, proficiency with data analysis tools (JMP, Excel), and cross-functional leadership across R&D, Regulatory, Manufacturing, and Engineering teams.

The Product & Test Engineer will validate and debug new silicon, develop ATE hardware and software solutions, and characterize device performance across process and operating conditions. The role involves cross-functional collaboration to develop test methodologies for advanced packaging technologies and release cost-effective production test solutions to mass production.…See more Required qualifications include a Bachelor's degree in Computer Engineering or Electrical Engineering and 3+ years of silicon bring-up, high-volume manufacturing, or related hardware engineering experience. Experience with test equipment (oscilloscopes, spectrum analyzers, logic analyzers), ATE platforms like Advantest 93K SOC, and DFT techniques is preferred.

Staff QA Engineer role at Dexcom leading quality engineering for high-volume manufacturing automation, design control, and process validation. Responsibilities include interpreting FDA 21 CFR 820 and ISO 13485 requirements, architecting validation strategies, driving design transfer for commercial deployment, leading complex investigations and CAPA initiatives, and mentoring cross-functional teams.…See more Requires deep expertise in root cause analysis, Six Sigma, process validation, statistical analysis, and data-driven decision-making across global sites.

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.…See more 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.

Staff QA Engineer at Dexcom leading manufacturing quality engineering and design control for high-volume medical device automation. The role requires deep expertise in FDA 21 CFR 820 and ISO 13485 compliance, design transfer strategy, process validation, and CAPA/MRB leadership across global manufacturing sites.…See more You will mentor cross-functional teams, drive systemic quality improvements, and represent the organization during regulatory inspections, with strong emphasis on data-driven decision-making and risk-based design methodologies.

Design and develop software applications that orchestrate complex automated laboratory workflows and closed-loop learning systems for biotherapeutics discovery. Build data pipelines, visualization tools, and machine learning models for visual inspection, predictive maintenance, and process optimization.…See more Implement IoT integrations, digital lab twins, telemetry systems, and maintain integrations across automation schedulers, LIMS, and data platforms using DevOps best practices and cloud solutions. Requires a Ph.D. in Computer Science, Software Engineering, or Bioengineering with 3+ years of industry experience (or equivalent M.S./B.S. with 10+/13+ years respectively), strong proficiency in Python, SQL, and JavaScript, and experience with lab digitalization and autonomous systems.

This Systems Integration Engineer II/III role centers on hands-on system validation, verification, and reliability testing for complex life-science instrumentation integrating hardware, software, firmware, optics, lasers, fluidics, and motion control. The engineer will conduct cross-functional troubleshooting, execute structured test protocols, analyze instrument performance data using statistical methods and Python, and document findings to drive design improvements and field support readiness.…See more Key responsibilities include evaluating workflows against real customer use cases, performing root-cause analysis on failure modes, and continuously refining integration documentation and testing practices. The role requires 2–5 years of systems integration or testing experience, proficiency in DOE/FMEA/statistical analysis, and hands-on lab work with prototypes and integrated instruments.

Lead complex quality investigations and root cause analysis for a medical device company, driving CAPAs, NCMRs, and systemic corrective actions. Provide technical leadership in quality engineering methodologies including Six Sigma, Lean Manufacturing, process capability analysis, and risk-based problem solving.…See more Own validation and qualification strategies for equipment, processes, test methods, and software V&V across the product lifecycle. Partner with R&D, Regulatory Affairs, Manufacturing, and Engineering teams on design transfer, commercialization, and compliance initiatives while representing Quality during audits and regulatory inspections.

Staff Reliability Engineer at Qualcomm responsible for developing and executing reliability engineering strategies, performing failure analysis, and applying statistical reliability modeling to influence product and technology decisions. Requires 4+ years of reliability engineering experience (or equivalent with advanced degree) and 1+ year in a technical leadership role.…See more The role demands expertise in Design-for-Reliability (DfR), reliability physics, failure mechanisms, and statistical analysis methodologies, with experience in semiconductor, packaging, or electronic system technologies highly valued.

Design and develop software applications orchestrating complex automated laboratory workflows, closed-loop learning systems, and AI-integrated autonomous discovery ecosystems for biotherapeutics research. Build data pipelines, visualization tools, and machine learning models for visual inspection, predictive maintenance, and process optimization.…See more Create digital lab infrastructure including IoT integrations, digital lab twins, telemetry monitoring, and integrations across automation schedulers, LIMS, and data platforms. Requires Ph.D. in Computer Science/Software Engineering/Bioengineering with 3+ years industry experience (or M.S. with 10+ years, or B.S. with 13+ years), preferably in pharmaceutical or automation sectors.

As Senior Staff Quality Engineer at Dexcom, you will drive quality compliance and inspection readiness across products, processes, and systems in a medical device environment. You'll lead complex investigations, implement corrective and preventive actions, mentor engineers, and ensure adherence to FDA 21 CFR 820 and ISO 13485 requirements.…See more The role requires hands-on expertise in QMS frameworks, design control, regulatory inspections, and the ability to influence stakeholders across engineering, operations, and global sites to maintain continuous audit readiness.

This Staff QA Engineer role leads the design, development, validation, and deployment of Quality Assurance metric dashboards for manufacturing operations, with expertise in medical device quality management systems (QMS), regulatory compliance (FDA 21 CFR Part 11, ISO 13485), and non-conforming event management. The position coordinates site and corporate management reviews, participates in internal and external audits, and supports cross-functional teams in CAPA, risk management, and validation activities.…See more The engineer applies statistical analysis and dashboard tools (Power BI, Tableau, SQL, BigQuery) to drive quality decisions and operational excellence. Success requires direct experience with QMS, nonconforming materials, auditing, medical device regulations, and the ability to lead diverse functional groups in a fast-paced environment.

Design and develop software applications that orchestrate complex automated laboratory workflows and closed-loop learning systems for biotherapeutics discovery. Build data pipelines, visualization tools, and machine learning models for visual inspection, predictive maintenance, and process optimization.…See more Create digital lab infrastructure including IoT integrations, digital lab twins, and telemetry monitoring. Requires a Ph.D. in Computer Science, Software Engineering, or Bioengineering with 3+ years of industry experience, or equivalent education with more experience; strong proficiency in Python, SQL, JavaScript, and DevOps practices; and familiarity with lab data platforms and autonomous systems.