Senior Biocompatibility Scientist II Regulatory Risk Expert
Abbott
Abbott in Santa Clara seeks a Senior Biocompatibility Scientist II to lead biocompatibility evaluations for medical devices and materials, ensuring patient safety across the product lifecycle and regulatory compliance (ISO 10993, ISO 14971, FDA guidance). This senior individual contributor role collaborates with cross-functional teams, reviews data, prepares reports, supports regulatory submissions, and maintains up-to-date knowledge of standards while adhering to Abbott policies and quality #J-18808-Ljbffr Abbott
$100k - $200k
...female executives, and scientists For years, Abbott’s... ...Description As a Senior Biocompatibility Scientist II, you will play a... ...as a Subject Matter Expert (SME) in biocompatibility... ...with global regulatory requirements, including... ...and assess project risks, recommending...SeniorRiskRegulatoryFor contractorsLocal areaShift work- ...teams (engineering, product development, regulatory, post-market surveillance) to define and... ...interpret and summarize published data on risks, alternate therapies and device-specific... ...licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
$160k - $240k
What You’ll Do 23andMe is looking for a Sr. Scientist II to join our Lung cancer research team. This Scientist will provide scientific input... ...company with multiple FDA authorizations for genetic health risk reports. The company has created the world’s largest crowdsourced...SeniorRiskWork at officeLocal area3 days per week$112k - $152k
...they love.Position Overview The Senior Microbiologist will serve as a subject-matter expert for microbiological safety across... ...strategies, lead testing and risk assessments, support product and... ...ensure compliance with applicable regulatory and quality requirements. The ideal...SeniorRiskRegulatoryContract workLocal areaImmediate start- ...Translational Research Scientist to lead efforts to understand... ...a portfolio of Class II and III medical devices... ...into device design, regulatory submissions, and... ...manufacturing teams to de-risk devices and accelerate... ...Identify subject matter expert collaborators. Build and...SeniorRiskRegulatoryContract workLocal areaRemote workWork from homeWorldwideRelocationHome officeFlexible hours
- ...Translational Research Scientist to lead efforts to understand... ...a portfolio of Class II and III medical devices... ...into device design, regulatory submissions, and... ...manufacturing teams to de‑risk devices and accelerate... ...• Act as the internal expert on clinical application...SeniorRiskRegulatory
$240k - $334k
...facilitate information sharing amongst domain experts, fostering a culture of execution... ...including a strong understanding of technical risks and security requirements for AI agents.... ...frameworks, data governance, or regulatory compliance within infrastructure.A problem...SeniorRiskRegulatoryWork at office- ...Function of PositionThe Senior Manager of Instruments... ...creativity, risk taking, and crisp executionDevelop... ..., Supplier, Quality, Regulatory Affairs and Marketing... ...in biocompatibility principles and regulatory... ...take 3 to 6+ months) or (ii) implement a Technology...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...Function of Position:The Senior Project Manager -... ...medical device development, regulatory pathways, operations, sterilization, biocompatibility, and cross-functional... ...project plans, schedules, risks, and resource... ...take 3 to 6+ months) or (ii) implement a Technology...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...suffering from BPH are treated? Join us as a Senior Regulatory Affairs Specialist and be at the... ...regulatory strategies for new and modified Class II and III devices and preparing and... ...international geographiesAbility to identify risk areas and escalate issues as...SeniorRiskRegulatoryFull time
$166.95k - $181k
...physicians, and cross‑functional teams. The senior scientist will serve as a hands‑on program leader... ...are met while proactively managing risks and operational complexity. The role... ...and aligned with downstream publication, regulatory, and commercialization needs. Ensure compliance...SeniorRiskRegulatoryWork at office- ...DescriptionPrimary Function of Position:The Senior Project Manager - Advanced... ...rigorous design, clinical, regulatory requirements and... ...and resource allocation, and risk assessment for advanced energy... ...can take 3 to 6+ months) or (ii) implement a Technology Control...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...expertise and guidance on design controls, risk management, process validation, and... ...processes and all external design control and regulatory requirements. Roles & Responsibilities:... ...licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...DescriptionPrimary Function of Position The Senior Quality Engineer supports... ...lifecycle, design controls, risk management, anomaly tracking... ..., and traceability matrices.Regulatory Support:Support Regulatory... ...can take 3 to 6+ months) or (ii) implement a Technology Control...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
$130k - $260k
..., and brand through proactive risk management is essential. Our Seller... ...patterns.What you'll do...The Senior Director of Emerging Threats... ...with Compliance, on level II monitoring and Risk Oversight... ...managementAbility to navigate evolving global regulatory and compliance requirements....SeniorRiskRegulatoryFull timeTemporary workPart time- ....Actively participate in design reviews, risk assessments, and failure analysis discussions... ..., test reports, and DHF content.Support regulatory and quality-system requirements... ...licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“TCP...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...Function of the PositionThe Senior Clinical Development... ...Systems to become an expert within the company on the... ...and document clinical risks, and identify... ...of new productsSupport regulatory documentation and submissions... ...take 3 to 6+ months) or (ii) implement a Technology...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...instruments platforms. This Senior Mechanical Design... ...reliability, manufacturability, risks, and clinical needs.... ...your area; support regulatory and standards... ...interviews with clinical experts to inform designs.Stay... ...take 3 to 6+ months) or (ii) implement a Technology...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...engineering, design, human factors, and regulatory affairsFacilitate and ensure that complex... ...resourced, and communicated to minimize risk, deliver on-time and on-budgetFunction as... ...licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
$182.36k - $273.2k
...optimized low-power techniques.We are seeking a SoC / RTL Low-Power Expert who serves as the final technical authority for power behavior... ...closure on large designsAbility to predict power behavior and risks before tool analysisExperience resolving conflicting power data...SeniorRiskPermanent employmentFull timeInternshipWork from home$161k - $221k
...practices to improve products, processes or servicesLeadershipMay lead functional teams or projects with moderate resource requirements, risk, and/or complexity Problem SolvingLeads others to solve complex problems; uses sophisticated analytical thought to exercise judgment...RiskFull time- ...procurement, supplier engineering, quality, and regulatory.The Mechanical Engineer, Wiring Harness... ...FOS that is proportional to the risk associated with the specific partRapid development... ...process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“...SeniorRiskRegulatoryWork experience placementLocal areaWorldwideFlexible hours
- ...the PositionThe Digital Senior Clinical Development... ...insights into requirements, risk assessments, validation... ...Systems to become an expert within the company on... ...human factors, product, regulatory, and quality teams to define... ...3 to 6+ months) or (ii) implement a Technology...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...instrument/accessories manufacturing line from a risk perspective (PFMEA) to incorporate and... ...development, planning, purchasing, regulatory, inspection, customer support and clinical... ...licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“...SeniorRiskRegulatoryWork experience placementLocal areaWorldwideFlexible hours
- ...meet stringent clinical, functional, global regulatory (FDA, ISO 11607, EU), and quality... ...and test components, including performing risk analyses and developing design requirements... ...licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“...SeniorRiskRegulatoryFor subcontractorLocal areaWorldwideFlexible hours
- ...Intuitive Ion Human Factors team, the Senior Human Factors Engineer works... ..., technical product managers, regulatory affairs, and other important... ...and characterize use-related risks, conduct usability testing of... ...can take 3 to 6+ months) or (ii) implement a Technology...SeniorRiskRegulatoryLocal areaWorldwideFlexible hours
- ...enable scalable contracting processes and advise on regulatory issues affecting global growth. You will report to... ...Managing Associate General Counsel and serve as a senior contributor embedded with the team, handling risk, compliance, and strategic guidance with #J-18808-...SeniorRiskRegulatory
$141k - $193.5k
...is offering a career‑growth opportunity for an experienced Senior Supply Chain expert. This role involves structuring and managing high‑complexity... ...discussions to solve complex problems and associated risks; use a structured approach and advanced analytical thinking...SeniorRiskFull time- ...issues.Create, review, and revise Risk Management documents such as... ..., planning, purchasing, regulatory, inspection, customer support... ...can take 3 to 6+ months) or (ii) implement a Technology Control... ...ManufacturingExperience level: Mid-Senior LevelIndustry: Medical DeviceSeniorRiskRegulatoryLocal areaWorldwideFlexible hours
$192k - $304.75k
We are now looking for Senior Research Scientist, Security and Privacy. NVIDIA is seeking exceptional security and privacy researchers to contribute... ...:Understand and analyze the potential vulnerabilities and risks in future systems for AI and AI-based systems.Develop...SeniorRiskFull time
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