Contracted Services Administrator Stanford UniversityContracted Services AdministratorStanford, CA$100,114–$110,747 / yearContracted Services supports a diverse, high-volume portfolio of contracted services, including custodial, elevators, pest control, roofing, loading dock equipment, dock levelers, roll-up doors, fire doors, and other facility services. Prepare and maintain accurate written documentation, including emails, meeting notes, inspection reports, service updates, action items, customer replies, handwritten field notes, and tracker entries.
Senior Quality Engineer Medical Device External Quality AbbVie IncSenior Quality Engineer Medical Device External QualityPleasanton, CAOversee CMOs and/or third-party suppliers to ensure that non-conformances, CAPAs, Reworks, and deviations are accurately documented, reviewed, and approved as well as resolving compliance issues related to commercial product and/or custom components. As such, the Manager, Medical Device External Quality works closely with AbbVie's Contract Manufacturing Organizations (CMOs), relevant third-party suppliers (e.g., custom components and finished devices), and internal stakeholders to ensure compliance with defined specifications and regulatory requirements.
PMCM Practice Leader T.Y. Lin International Group LtdPMCM Practice LeaderSan Francisco, CA$215,000–$296,000 / yearIn conjunction with the Practice Leadership Team, utilizing key partners in Shared services including Talent Attraction Leaders and HR Business Partners, identifies strategic hires and talent development needs, by defining strategic workforce gaps, and participates in the attraction and acquisition of key hires. Partnering with the Leadership Team, influences, guides, and coaches the development and cultivation of a best-in-class team of managers, project managers and field staff to collectively support the objectives of the strategic plan.
Senior QMS Specialist Skydio, Inc.Senior QMS SpecialistHayward, CA$147,000–$210,000 / yearThe Skydio team combines deep expertise in artificial intelligence, best-in-class hardware and software product development, operational excellence, and customer obsession to empower a broader, more diverse audience of drone users, from utility inspectors to first responders, soldiers in battlefield scenarios, and beyond. Strengthening audit readiness and outcomes with proactive compliance management leads to smoother audits, fewer findings, and stronger relationships with customers and certification bodies.
Senior QMS Specialist SkydioSenior QMS SpecialistHayward, California$147,000–$210,000 / yearThe Skydio team combines deep expertise in artificial intelligence, best-in-class hardware and software product development, operational excellence, and customer obsession to empower a broader, more diverse audience of drone users, from utility inspectors to first responders , soldiers in battlefield scenarios , and beyond . Strengthening audit readiness and outcomes with proactive compliance management leads to smoother audits, fewer findings, and stronger relationships with customers and certification bodies.
Quality Technician - (108267) SanminaQuality Technician - (108267)San Jose, CA$60,320–$68,640 / hourRecognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors. The total rewards package also includes a variety of benefits, including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business and, depending on the role, may include eligibility for restricted stock unit awards and participation in a discretionary bonus program.
Quality Technician - (108264) SanminaQuality Technician - (108264)San Jose, CA$60,320–$68,640 / hourRecognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors. The total rewards package also includes a variety of benefits, including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business and, depending on the role, may include eligibility for restricted stock unit awards and participation in a discretionary bonus program.
Quality Technician - (108268) SanminaQuality Technician - (108268)San Jose, CA$60,320–$68,640 / hourRecognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors. The total rewards package also includes a variety of benefits, including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business and, depending on the role, may include eligibility for restricted stock unit awards and participation in a discretionary bonus program.
NewSenior Regulatory Affairs Specialist – Heart Failure (on-site) AbbottSenior Regulatory Affairs Specialist – Heart Failure (on-site)Pleasanton, CaliforniaThe individual may execute tasks and play a consultative role by partnering across business functions as well as assist in identifying data needed, obtaining this data and ensuring that they are effectively presented for the registration of products worldwide. At Abbott’s Heart Failure (HF) business, we pioneer and increase access to lifesaving, connected innovations that empower people to take control of their health by delivering seamless clinical solutions from diagnosis to monitoring and treatment.
Embedded Release Engineer Manpower EngineeringEmbedded Release EngineerFoster City, CA$90–$95 / hourTemporaryManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.
QA Specialist - Full Time & Temporary Asahi Kasei Advance AmericaQA Specialist - Full Time & TemporaryFremont, California$36–$48 / hourOur business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. The position requires diverse skill sets and will provide the opportunity to challenge an individual's abilities to perform investigations, self-inspection audits, and analytical data review to maintain and expand Quality Control capabilities.
Senior Manager, GxP Electronic System Validation QA Revolution Medicines IncSenior Manager, GxP Electronic System Validation QARedwood City, CA$164,000–$205,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The Opportunity: Serve as the Computer System Validation (CSV) QA subject matter expert and provide guidance on the interpretation and application of global GxP regulations and guidance related to computerized systems, electronic records, electronic signatures, and data integrity, including FDA 21 CFR Part 11, EU Annex 11, and GAMP principles.
Director, GLP Quality Assurance Revolution MedicinesDirector, GLP Quality AssuranceRedwood City, CaliforniaThe company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The Director, Good Laboratory Practice Quality Assurance (GLP QA) is responsible for ensuring Good Laboratory Practices (GLP) compliance at RevMed and external vendors contracted to perform regulated work on behalf of RevMed including all GLP vendors.
Senior Quality Control Manager AntheiaSenior Quality Control ManagerMenlo Park, CAThe QC Manager also serves as the primary interface between internal teams and third-party testing partners (CDMOs, CROs, Contract Labs), overseeing the quality and timeliness of deliverables and driving resolution of analytical issues. Backed by leading investors and recognized by the U.S. government as a priority technology for public health and national and economic security, Antheia is manufacturing the medicines the world needs today while enabling tomorrow’s breakthrough therapeutics.
Sr. Manager, Tech Quality Assurance – Lingo (on-site) AbbottSr. Manager, Tech Quality Assurance – Lingo (on-site)Alameda, California$130,700–$261,300 / yearOur portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Lead, oversee or contribute to multiple portions of the Quality System, including but not limited to Design controls, software development, risk management, Product changes, product Release, NC/CAPA, and others as needed.
Senior Assurance Associate - Audit Innovation Nace AISenior Assurance Associate - Audit InnovationPalo Alto, CaliforniaYou'll apply your Big 4 audit expertise while pioneering AI integration in financial auditing, playing a critical role in shaping how artificial intelligence transforms audit quality and efficiency. Perform comprehensive financial audits and substantive testing procedures while leveraging AI-powered tools to enhance audit efficiency and accuracy.
Algorithm Assurance Technical Specialist - Global Security Organization TikTok IncAlgorithm Assurance Technical Specialist - Global Security OrganizationSan Jose, CAIn whatever ways users interact with us - whether they're watching videos on their For You page, interacting with a Live video, or buying products on TikTok Shop - GSO protects their data and privacy, so they can have a secure and trustworthy experience. Proven track record in successfully developing, implementing, and managing comprehensive compliance programs at scale with experience engaging directly with regulators, external auditors, or supervisory bodies on algorithmic or AI compliance matters.
Policy & Quality Specialist- ML Perception Data Waymo LLCPolicy & Quality Specialist- ML Perception DataMountain View, CA$152,000–$160,000 / yearDrive queue readiness & golden datasets: Speed up the initial labeling queue setup process by executing rapid policy iterations and hand-crafting golden datasets (small-scale baseline datasets of 10s of examples) to establish quality baselines before launching full-scale operations. Address edge cases & regional nuances: Provide critical, detailed inputs on long-tail edge cases and coordinate with regional country specialists to ensure country-specific driving rules and local nuances are accurately captured and validated, ahead of Waymo''s deployment in these new countries.
QA Specialist - Full Time & Temporary Bionique ScientificQA Specialist - Full Time & TemporaryFremont, California$36–$48 / hourOur business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. The position requires diverse skill sets and will provide the opportunity to challenge an individual's abilities to perform investigations, self-inspection audits, and analytical data review to maintain and expand Quality Control capabilities.
Senior QA Specialist, Global Document Control Management Revolution MedicinesSenior QA Specialist, Global Document Control ManagementRedwood City, CaliforniaThe company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Support strategic document management initiatives, including workflow optimization, system enhancements, document migrations, periodic reviews, global expansion activities, training programs, and process improvement projects.
Quality Assurance Specialist (Remote) UpshiftQuality Assurance Specialist (Remote)san francisco, CARemoteWe've been in business for 11 years and last year we helped over 250,000 Americans save money by going green. The role and responsibility of this role is to audit our sales agents calls and score them to provide a real time feedback mechanism.
NewConstruction (QA) Inspector - Airfield/Roadways Pavement ACCURA ENGINEERING & CONSULTING SERVICESConstruction (QA) Inspector - Airfield/Roadways PavementSan Francisco, CAPosition: Construction (QA) Inspector - Airfield/Roadways PavementLocation: San Francisco, CAJob Id: 66388# of Openings: 1Job Title: Construction (QA) Inspector – Airfield/Roadways Pavement***Work Location: Anchorage, AK***Salary: Based on experience and will be discussed with manager in interviewREQUIREMENT- Must be a US Citizen and must pass a federal background review and drug screenResponsibilities/Duties: Must have knowledge of airfield runway construction improvements and pavement resurfacing since detailed inspections must be made to ensure the required level of workmanship adhering to the contract, project plans and specificationsPerform and support three-phase inspection systemProvide daily QA reports to document all activities observed for each on-site day in sufficient detailReview and analysis of construction contractor progressEnsure safety requirements are met including EM 385-1-1 and OSHA requirementsReview of design, comment logging and back-checking; verify accurate as-built drawingsReview and comment on the accuracy of the construction contractor's requests for paymentReview and acknowledge daily reports including verification of the project schedule by indicating the activities worked on that day and the activities behind scheduleMaintain an Inspectors Site Inspection ReportAssist in response for Requests for Information (RFI), modifications and change ordersParticipate in pre-final and final inspections, assist in preparations of detailed punch-lists and check that all punch list items are corrected prior to final payment. Experience/Education: High School diploma is required or GED with at least 7 years of construction inspection experience performing quality assurance verification on construction contract, airfield runway improvements, roadways or pavement resurfacing experience highly preferredOr, Associate Degree (two-year degree) / Technical Training Degree (two years of training) with at least 5 years of construction inspection experience performing quality assurance verification on construction contract, airfield runway improvements, roadways or pavement resurfacing experience highly preferredOr, Bachelor of Science Degree and at least 3 years of construction inspection experience performing quality assurance verification on construction contract, airfield runway improvements, roadways or pavement resurfacing experience highly desiredPaving Inspector Certification provided by the Asphalt Institute will be required within 30 days of start date.
Director, GLP Quality Assurance Revolution Medicines IncDirector, GLP Quality AssuranceRedwood City, CA$211,000–$264,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The Opportunity: The Director, Good Laboratory Practice Quality Assurance (GLP QA) is responsible for ensuring Good Laboratory Practices (GLP) compliance at RevMed and external vendors contracted to perform regulated work on behalf of RevMed including all GLP vendors.
Senior Manager Product Development Quality Assurance CMC Product Lead AbbVie IncSenior Manager Product Development Quality Assurance CMC Product LeadSouth San Francisco, CAAs a team member in interdisciplinary product development teams (e.g., CMC teams), the Senior Manager is responsible for early identification and prevention of pipeline risks by driving consensus-building across AbbVie R&D functions and external partners. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paidand may be modified at the Company's sole and absolute discretion, consistent with applicable law.
QA Inspector 3 - FQA- Day Shift UNIGEN CORPORATIONQA Inspector 3 - FQA- Day ShiftNewark, CAFounded in 1991, we've grown into a leading provider of electronics manufacturing services (EMS), offering a comprehensive suite of solutions from design and manufacturing to supply chain management. Monitor and operate critical equipment and instrumentation: Read and interpret assembly drawings, BOMs, MPI, ECN, Deviation, and other manufacturing documentation.
Senior Manager, GxP Electronic System Validation QA Revolution MedicinesSenior Manager, GxP Electronic System Validation QARedwood City, CaliforniaThe company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Serve as the Computer System Validation (CSV) QA subject matter expert and provide guidance on the interpretation and application of global GxP regulations and guidance related to computerized systems, electronic records, electronic signatures, and data integrity, including FDA 21 CFR Part 11, EU Annex 11, and GAMP principles.
NewQA Test Engineer (Android / Lab-Based) TechDigitalQA Test Engineer (Android / Lab-Based)Mountain view, CACommand Line Tools: Well-versed in ADB (Android Debug Bridge) and Linux/Unix commands to inspect device states, push/pull files, and extract system logs (logcat) for debugging. Technical Collaboration: Use your strong communication skills to act as the bridge between the lab, development team, and partner engineering teams to clearly explain bugs and technical findings.
Business Development Manager (Bdm) | America (Player Support And QA) SideBusiness Development Manager (Bdm) | America (Player Support And QA)San Francisco, CAThis role focuses on expanding partnerships and revenue primarily across our player support and QA capabilities, while also touching on our full suite of game production services including Game Development, Art Production, Localization, Localization QA, Game Audio, Datasets, and IT services — serving console, PC, and mobile game developers, depending on end client needs. Sales & Account Growth Lead business development for player support and QA services — including live operations support, helpdesk solutions, functional testing, compliance, and certification — alongside our co-development capabilities spanning Game Development, Art Production, Game Audio, Localization, Localization QA, Datasets, and IT.
Business Development Manager (BDM) | America (Player Support and QA) SideBusiness Development Manager (BDM) | America (Player Support and QA)San Francisco, CaliforniaThis role focuses on expanding partnerships and revenue primarily across our player support and QA capabilities, while also touching on our full suite of game production services including Game Development, Art Production, Localization, Localization QA, Game Audio, Datasets, and IT services — serving console, PC, and mobile game developers, depending on end client needs. Sales & Account Growth Lead business development for player support and QA services — including live operations support, helpdesk solutions, functional testing, compliance, and certification — alongside our co-development capabilities spanning Game Development, Art Production, Game Audio, Localization, Localization QA, Datasets, and IT.
Director, QA Systems (Contract) Adverum Biotechnologies, Inc.Director, QA Systems (Contract)Redwood City, CALeveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians’ offices to eliminate the need for frequent ocular injections to treat these diseases. Actively partner with cross-functional leadership to address challenges, develop solutions, and execute plans for integration with corporate systems and preparation for commercial stage support.
Quality Assurance Lead CareDxQuality Assurance LeadBrisbane, CA$112,000–$140,000 / yearCareDx, Inc. is a leading precision medicine solutions company focused on the discovery, development, and commercialization of clinically differentiated, high-value healthcare solutions for transplant patients and caregivers. CareDx offers products, testing services, and digital healthcare solutions along the pre- and post-transplant patient journey, and is the leading provider of genomics-based information for transplant patients.
Quality Control Specialist Creative Critical Mass IncQuality Control Specialist CreativeSan Jose, CAYou will review a wide range of deliverables including static creatives, video assets, HTML emails, display banners, websites, mobile experiences, and other digital products. Validate assets across multiple formats, including static creatives, video, HTML banners, emails, websites, and digital experiences prior to release.
Sr. Manager, Quality Systems & Compliance Abbott LaboratoriesSr. Manager, Quality Systems & CompliancePleasanton, CA$148,700–$297,300 / yearDecision making that has an extended impact on work processes and outcomes, that could cause substantial expenditure of additional time, human resources, and funds and jeopardize future business activity. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Sr. Manager, Quality Systems & Compliance AbbottSr. Manager, Quality Systems & CompliancePleasanton, California$148,700–$297,300 / yearDecision making that has an extended impact on work processes and outcomes, that could cause substantial expenditure of additional time, human resources, and funds and jeopardize future business activity Required Qualifications . Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Software Development Engineer in Test Platform Safety Assurance Zoox IncSoftware Development Engineer in Test Platform Safety AssuranceFoster City, CA$138,000–$212,000 / yearThe ideal candidate is passionate about developing high-quality, robust, optimized, and reusable software infrastructure and is eager to advance their skills in complex systems thinking and validation problem-solving. Here at Zoox, we know that diverse perspectives foster the innovation we need to be successful, and we are committed to building a team that encompasses a variety of backgrounds, experiences, and skills.
QC Analyst II *PC 610 Miltenyi BiotecQC Analyst II *PC 610San Jose, CaliforniaMiltenyi Bioindustry plays a unique role as both the producer and the service provider, relying on our instruments and reagents for each workflow step, controlling the entire supply chain and thus delivering greater security and planning clarity to our customers. Your Role: This position is primarily responsible for the complete development, qualification and performance of environmental monitoring and microbiological QC assays to support GMP manufacturing operations in a Phase I/II multi-product biologics facility.
Real Estate Accounting Financial Analyst Stanford UniversityReal Estate Accounting Financial AnalystRedwood City, CA$116,995–$122,000 / yearThe individual will collaborate closely with internal departments, including Stanford Management Company, Stanford Land, Building, Real Estate, Faculty, Staff Housing, and external property managers, ensuring accurate and timely accounting and reporting for real estate assets. The pay offered to a selected candidate will be determined based on factors such as but not limited to the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget, availability, internal equity, geographic location, and external market pay for comparable jobs.
Risk Analyst - Grid Operations & Reliability, Principal - OGO/Fresno/Sacramento/Stockton PG&E CorpRisk Analyst - Grid Operations & Reliability, Principal - OGO/Fresno/Sacramento/StocktonOakland, CAThe Electric T&D Team is responsible for ensuring the electric grid's reliability and resiliency through the ongoing maintenance and operations of PG&E's 100,000 miles of distribution lines and over 18,000 miles of Transmission lines. Develops and maintains an asset risk register, coordinating with the various asset family owners across Electric T&D, to track operational and enterprise risks and the execution and effectiveness of risk mitigation activities.
Senior Operations Finance Analyst PG&E CorpSenior Operations Finance AnalystOakland, CAThe Operations Finance department provides a unique environment for energized and talented finance professionals to engage in the business as valued functional advisors, make meaningful contributions to the direction of a dynamic business, and be actively developed and recognized. This role will be placed within the Operations Finance organization supporting Electric Operations; a high performing, fast paced organization redefining the functional value proposition through engaged, innovative, and actionable insight.
Senior Project Controls Analyst TD ThorntonSenior Project Controls AnalystSan Francisco, CA$130,000–$150,000 / yearWe welcome applicants from engineering, construction management, project management, business analytics, scheduling, and anyone who thrives in a collaborative environment Job Overview Title: Senior Project Controls Analyst Sector: Electric Utilities Seniority: Senior Location: San Francisco, CA Work Type: Hybrid (1-2 days per week in office) TD Thornton is seeking a highly skilled Senior Project Controls Analyst to oversee cost, schedule, and scope management across a portfolio of major construction projects in the electric utilities sector. Whether we are part of the contractor's team or serving as an owner's representative, we offer a wide spectrum of construction management support services to help our clients mitigate risks and deliver successful project outcomes.
Legal Administrative Assistant Shook Hardy & Bacon LLPLegal Administrative AssistantSan Francisco, CAProvides administrative, organizational and technical support including but not limited to entering time into the firm's timekeeping system, phone reception; providing information to callers; arranging travel and catering accommodations; scheduling meetings and conference room set ups; e-scan, facsimile, ECF filing transmittals; transcription; proofreading work product for typographical, grammatical, or spelling errors; compilation of reports from established sources; photocopying; mail assembly and distribution; and other records/file maintenance. Depending on the specific assignment, may prepare and/or review for accuracy patent and trademark applications, reports, documentation, general and/or legal correspondence and papers of a legal nature such as, complaints, brief, motions, interrogatories, contracts, agreements, statements, subpoenas, wills, trusts, summonses.
Sr. Software Reliability & Stability Quality Engineer, Siri Speech Apple IncSr. Software Reliability & Stability Quality Engineer, Siri SpeechCupertino, CAStrong interpersonal skills to work well with engineering teams Excellent problem solving and critical thinking Ability to work in a fast-paced environment with rapidly changing priorities Passionate about building extraordinary products and experiences for our users. Experience building and deploying production-grade AI agent systems Improving workflows using AI tools Experience in building automated UI and non-UI tests for user facing applications or system frameworks.
NewASIC Design Verification Manager, Google Cloud Google LLCASIC Design Verification Manager, Google CloudSunnyvale, CAFrom software to hardware our teams are shaping the future of world-leading hyperscale computing, with key teams working on the development of our TPUs, Vertex AI for Google Cloud, Google Global Networking, Data Center operations, systems research, and much more. Guide the functional verification team for portions of TPU designs, setting and communicating individual and team priorities that support organizational goals, providing regular feedback and coaching, and developing functional verification infrastructure across subchip, subsystem, and fullchip level environments.
NewData Collection Quality Support FigureData Collection Quality SupportSan Jose, CaliforniaYou will review data collection sessions, identify quality issues, and produce assessment reports that give team leaders clear, actionable insight into pilot performance. Identify and document issues including technique inconsistencies, incomplete sequences, and edge-case scenarios.
Teleops Quality Support FigureTeleops Quality SupportSan Jose, CAYou will review teleop data collection sessions, identify quality issues, and produce assessment reports that give team leaders clear, actionable insight into pilot performance. Identify and document issues including technique inconsistencies, incomplete sequences, and edge-case scenarios.
APeX Application Analyst - Willow UCSF Medical CenterAPeX Application Analyst - WillowSan Francisco, CAIn addition to general system support and maintenance this position will be heavily involved in areas of medication billing including but not limited to processing medication receiving, billing error resolution, medication cost updates, 340b build maintenance, HCPC maintenance, and follow up to billing related inquiries. Key technical activities include the analysis of new releases to determine how workflow should be modified, building and populating databases and tables during initial system configuration, conducting system testing and conversion data validation.
Quality Systems and Compliance Lead Verily Life Sciences LLCQuality Systems and Compliance LeadSan Bruno, CALeads the ongoing vision and implementation of the Quality Management System (QMS) - spanning consumer, research, and medical device (SaMD) quality, including AI/ML-enabled and generative AI products - in conformance with domestic and international GMP, GCP, GCLP, and GLP regulatory requirements and industry best practices applicable to the portfolio of products and services supported. Partners with engineering and product teams to embed quality practices into software development workflows; experience with Jira and GitHub (or equivalent tools) is a plus for supporting SaMD and AI/ML quality processes including change control, issue tracking, and Design and Development File management per ISO 13485:2016.
Senior Manager, GMP Quality Revolution Medicines IncSenior Manager, GMP QualityRedwood City, CA$164,000–$205,000 / yearThe Opportunity: Revolution Medicines is seeking a Senior Manager, GMP Quality who will play a key role within Quality Assurance and is responsible for providing leadership and operational support for RevMed programs through different phases of development, with a strong emphasis on Quality Control aspects associated with clinical and commercial products. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.
Senior Manager, GMP Quality Revolution MedicinesSenior Manager, GMP QualityRedwood City, California$164,000–$205,000 / yearRevolution Medicines is seeking a Senior Manager, GMP Quality who will play a key role within Quality Assurance and is responsible for providing leadership and operational support for RevMed programs through different phases of development, with a strong emphasis on Quality Control aspects associated with clinical and commercial products. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.
Sr. Software Analyst, Data, Autonomy Rivian Automotive IncSr. Software Analyst, Data, AutonomyPalo Alto, CA$132,100–$165,100 / yearRivian may use your Candidate Personal Data for the purposes of (i) tracking interactions with our recruiting system; (ii) carrying out, analyzing and improving our application and recruitment process, including assessing you and your application and conducting employment, background and reference checks; (iii) establishing an employment relationship or entering into an employment contract with you; (iv) complying with our legal, regulatory and corporate governance obligations; (v) recordkeeping; (vi) ensuring network and information security and preventing fraud; and (vii) as otherwise required or permitted by applicable law. Utilize dashboards and reports to monitor: Annotation throughput, efficiency, and cost Quality metrics (QA pass rates, error types, rework) Vendor and annotator performance trends Interpret complex annotation and perception data into clear, actionable insights for engineering, annotation operations, and leadership.