Medical Device Software Quality Engineer — Compliance & Risk
Real
Real is seeking a Software Quality Engineer located in California, Missouri. The role involves supporting the software development life cycle with a focus on quality oversight, compliance, and risk management. Ideal candidates will have 4-5 years of experience, including 1-2+ years in medical device software, and be knowledgeable about IEC 62304 standards. Benefits may include health insurance, retirement plans, and paid leave, subject to location and hire date. #J-18808-Ljbffr Real
- ...We are seeking a Software Quality Engineer to support and oversee the software... ...2+ years of experience in medical device software Working knowledge... ...Familiarity with software risk management practices Additional... ...on quality oversight, compliance, and risk , rather than...RiskMedical device
$127k - $165k
About This Role The Staff Software Quality Engineer for Non-Product Software (... ...strategy, validation, and compliance of software tools used in... ...development and manufacturing of Medical Device. This role ensures that... ...non-product software. Risk Management: Apply risk-...RiskMedical deviceWork experience placement$90k - $180k
...the Role We are seeking a Software Test Engineer to lead verification and... ...within a regulated medical device environment. This role is... ...role in ensuring product quality, regulatory compliance, and scalable delivery.... ...verification strategies. Support risk management activities,...RiskMedical device- ...Inc is seeking a Supplier Engineer in California to support supplier... ...material validation for medical devices. The ideal candidate will... ...collaborate with suppliers to ensure quality and compliance. Responsibilities include... ...material evaluation, risk assessments, and developing...RiskMedical device
- ...is seeking a Senior Director of Quality to provide strategic leadership... ...quality systems, regulatory compliance, and continuous improvement within a growing medical device organization. You will lead quality... ...environments, audits, CAPA, risk management, and scalable #J-18...RiskMedical device
- Supplier Quality Engineer - Medical Device Location: Irvine, CA (Onsite) Duration: 12-Month Contract We... ...Supplier Engineering to ensure quality and compliance throughout the supply chain. Key... ...implementation Evaluate supplier risk level and maintain approved supplier...RiskMedical deviceContract work
- ...47. We have Contract role Quality Engineer for our client at Santa Clara... ...This role will provide compliance support to the Regulatory Affairs... ...identification of risks, mitigation of risks identified... ...implementing mitigations. Exposure to Medical Device US and CE regulations,...RiskMedical deviceContract work
- ...About This Role:**The Quality Control Manager is... ...Control Manager ensures compliance with applicable... ...compliance and audit risk related to inspection... ...collaboration with Quality Engineering, Supplier Quality and... ...experience in a medical device manufacturing environment...RiskMedical device
- ...functional partners. You will leverage data-driven insights to identify risks and enhance product quality across global markets. The ideal candidate should have at least 5 years of experience in the medical device industry, a Bachelor’s degree in a relevant field, and...RiskMedical deviceWork at office
$75.1k
...culture by modeling high-quality work, effective... ...oriented thinking. Ensure compliance with U.S. and... ...regulatory requirements for medical device complaint handling... ...and collaborate with engineering, laboratory and other... ...analytics to identify risks, opportunities and...RiskMedical deviceWork at officeRelocation package3 days per week$92k - $130k
...patient’s life. Our Quality teams help shape... ...patient care with devices supported by clinical... ...supporting medical device manufacturing... ...actions to ensure compliance with regulatory, quality... ..., or risks within microbiology... ...laboratory equipment software (e.g. LIMS, WinKQCL...RiskMedical device$70k - $88k
...safely, efficiently, and in compliance with all quality and regulatory standards.... ...with Manufacturing Engineering, Quality, and Supply Chain... ...delivery of high‑quality medical devices that improve patients’ lives... ...them early. Take Calculated Risks: Use sound judgment when making...RiskMedical deviceShift workWeekend workAfternoon shift$181.2k - $344.3k
...the Neuromodulation Quality Systems team to ensure... ..., meeting regulatory compliance requirements. Onsite... ...team fostering CAPA, risk management, management... ...across Production, Engineering, Corporate, Regulatory... ...years operating in a medical device quality systems environment...RiskMedical deviceWork experience placementWork at office$158k - $252k
...Direct & Indirect purchases, and ensure quality and regulatory compliance. Specific Job Responsibilities Lead... ...and strategic alliances. Develop risk management strategies to mitigate supply... ...sourcing. Seven or more years in Medical Device, Pharma, or Biotech with thorough...RiskMedical deviceFull timeContract workTemporary workShift work$75.1k - $142.6k
...insights to identify risks, improve processes, and... ...that enhance product quality and performance... ...oriented thinking. Ensure compliance with U.S. and... ...regulatory requirements for medical device complaint handling... ...and collaborate with engineering, laboratory, and other...RiskMedical deviceWork at office$90k - $105k
...is a California-based global medical device company dedicated to... ...stay transparent, prioritize quality, and own our actions. Innovation... ...Boldness Propels Us: We take smart risks and are unafraid in our... ...continuous improvement, and quality/compliance objectives. This role...RiskMedical deviceFor contractorsWork at officeLocal areaRemote workWork from homeFlexible hours$90k - $180k
Abbott Laboratories in California is seeking a Software Test Engineer to lead verification efforts in a regulated medical device environment. The position includes ensuring product quality, regulatory compliance, and developing robust testing strategies. Required qualifications...Medical device- ...Specialist for a remote position in California. This role involves assessing product safety risks, managing complaints, and ensuring compliance with regulatory requirements in the medical device industry. A successful candidate will have 3-5 years of experience in a regulated...RiskMedical deviceRemote work
- ...inventory health targets and supply risk optimization. Co‑leads... ...collaboration from Supplier Engineering. Leverages knowledge of... ...cost of ownership and high‑quality product while identifying value... ...Experience Experience in the medical device industry preferred. SAP and...RiskMedical deviceContract workLocal area
- A leading global medical device company seeks a Sr. Director, Compliance in California to oversee its healthcare compliance program. The role includes managing... ...offers competitive compensation and assesses compliance risks to drive continuous improvement. #J-18808-Ljbffr...RiskMedical deviceRemote job
- A biotechnology/medical device company is seeking a Validation Engineer to lead validation activities for products and processes in Ventura County... ...developing test methods, conducting risk assessments, and ensuring compliance with regulations. The ideal candidate will...RiskMedical device
$30 - $45 per hour
...the pharmaceutical and medical device industries. Whether... ...computerized systems, ensuring compliance with FDA, GxP, and 21... .... Process Validation Engineers - Strong background in process development, risk analysis, and... ...Contract Job function Quality Assurance Industries...RiskMedical deviceContract workRemote workFlexible hours- Responsibilities Manage patient claims related to its Medical Device businesses. Lead day-to-day claim adjudication. Drive compliant, consistent... ...of matters presenting regulatory, litigation, or safety risk. Execute comprehensive investigations to determine causation,...RiskMedical device
- ...experienced Supplier Engineer to support supplier qualification... ...improvements for medical device products. The ideal... ...changes, perform risk assessments, develop and... ...suppliers continue to meet quality and regulatory... ...inspection methods to ensure compliance with company and...RiskMedical device
$48 per hour
...motivated Senior Manufacturing Engineer, NPI to join it in advancing... ...NPI reviews with R&D, Quality, and Production teams to ensure... ...timelines, proactively identifying risks and implementing mitigation... ...assemblies strongly preferred Medical device industry experience preferred...RiskMedical deviceHourly payFull timeLocal area- ...forward-thinking and ambitious engineers to accelerate their careers... ...pharmaceutical, biotechnology, and medical device industries. We offer an... ...validation protocols, reports, and risk assessments in accordance... ...expectations, internal quality standards, and audit readiness...RiskMedical deviceContract work
- ...financial, operational, and quality metrics Monitor vendor performance... ...performance, identify risks, and drive continuous... ...Procurement, Finance, Legal, Compliance) to manage vendor relationships... ...Background in healthcare, medical device, or regulated environments preferred...RiskMedical deviceContract work
- ...Supplier Quality Engineer – PBCBA / Electromechanical Devices Key Responsibilities :Manage supplier... ...electromechanical component s used in medical devices or highly... ...suppliers to ensure compliance with quality standards,... ...supplier change notifications, risk assessments, and...RiskMedical device
$80k - $97.5k
...time position is with a thriving medical device company looking to expand their quality assurance department! Please see... ...Responsibilities: Develop and maintain risk management files, including FMEAs... ...control. Qualifications: BS in Engineering or relevant experience in medical...RiskMedical deviceFull timeWork at officeRelocation- ...facilitate regulatory approvals. Provide risk-based guidance and regulatory input to... ...affairs experience working in a medical device company (can be in combination with a regulatory... ...Minimum B.S. or higher in Biomedical Engineering, Electrical Engineering, Mechanical...RiskMedical device3 days per week
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