QA Analyst II BC ForwardQA Analyst IIMenlo Park, CAFull timeWith delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity. BCforward is a leading global IT consulting and workforce solutions firm providing services and support to Fortune 500 and government clients.
QA Analyst III (Automation) BC ForwardQA Analyst III (Automation)Menlo Park, CA$65–$66 / hourFull timeThe ideal candidate will have strong experience in manual and automated testing, quality metrics, and cross-functional collaboration and a proven ability to own test execution, improve test processes, and drive defect resolution. With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.
QA Analyst II (Python) BC ForwardQA Analyst II (Python)Menlo Park, CAFull timeThe ideal candidate will have strong experience in manual and automated testing, test planning, and quality metrics and a proven ability to own test execution, collaborate with engineering, and drive bug resolution. With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.
QA Analyst III (Networking Apps) BC ForwardQA Analyst III (Networking Apps)Menlo Park, CAFull timeThe ideal candidate will have strong experience in manual and automated testing, test strategy, and quality metrics and a proven ability to own test execution, improve processes, and drive defect resolution. With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.
NewSenior Manager, GCP & GVP, QA - Remote Agios PharmaceuticalsSenior Manager, GCP & GVP, QA - RemoteSan Francisco, CARemote$131,035–$196,553 / yearConduct and/or oversee consultant auditors in the conduct of GCP/GVP audits of clinical trial internal and PV processes, GCP/GVP vendors, clinical investigator sites, clinical study documents and trial master files in accordance with annual audit plans. The current base salary range for this position is expected to be between $131,035 and $196,553 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.
QA Analyst I (Mobile Testing) BC ForwardQA Analyst I (Mobile Testing)Menlo Park, CAFull timeThe ideal candidate will have experience in executing and developing test plans, test cases, and test scripts and a proven ability to identify, document, and track software defects to resolution. With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.
Lead Software Engineer Visa Technology and Operations LLCLead Software EngineerFoster City, CA$192,300–$307,600 / yearVisa is a world leader in payments technology, facilitating transactions between consumers, merchants, financial institutions and government entities across more than 200 countries and territories, dedicated to uplifting everyone, everywhere by being the best way to pay and be paid. Leverage modern technologies to build the next generation of Payment Services, Transaction Platforms, Real-Time Payments, and Buy Now Pay Later capabilities.
NewPerformance Marketing Strategy & Incentives Lead - Contract TalentBurst, Inc.Performance Marketing Strategy & Incentives Lead - ContractSouth San Francisco, CA$70–$79.22 / hourWithin DMO, the Performance Marketing team leads the engagement and adoption of performance marketing principles with brand teams, ensuring that comprehensive training, tools, and methodologies meet brand goals and drive efficient, high-quality business outcomes at scale. Working closely with Digital & Data Analytics (DDA), Marketing Ops, Finance, and Marketing teams, this individual supports experiment and optimization evaluation, incentive program operations, measurement governance, dashboard reporting and stakeholder engagement.
NewDirector, Commercial Risk Evaluation and Mitigation Strategies (REMS) Lead - Remote Agios PharmaceuticalsDirector, Commercial Risk Evaluation and Mitigation Strategies (REMS) Lead - RemoteSan Francisco, CARemote$183,549–$230,312 / yearThe Director leads the development, implementation, and ongoing management of commercial related REMS activities to support compliance, patient safety, and effective execution across sales, field marketing, patient support, specialty distribution and other customer-facing teams. The current base salary range for this position is expected to be between $183,549 and $230,312 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.
NewAssociate Director, Safety Systems Lead, Medical Safety & Risk Management - Remote Agios PharmaceuticalsAssociate Director, Safety Systems Lead, Medical Safety & Risk Management - RemoteSan Francisco, CARemote$153,541–$230,312 / yearThe Associate Director, Safety Systems Lead will be responsible for all technical aspects of the safety database environment, supporting business requirements for case processing and submission compliance, facilitating and managing interfaces with other systems, providing data to all relevant parties, serving as the safety systems technical subject matter expert and overseeing relevant safety systems vendors. Ensure safety systems remain continuously compliant, validated, and inspection-ready by overseeing computer system validation (CSV) deliverables (e.g., Validation Plans, Summary Reports, UAT), partnering with QA on audit trails/evidence, and maintaining adherence to SOPs, GxP, ICH, FDA regulations, EU Annex 11, and 21 CFR Part 11.
NewSenior/Lead Software Engineer - Developer Experience C3 AISenior/Lead Software Engineer - Developer ExperienceRedwood City, CAC3 AI delivers a family of fully integrated products including the C3 Agentic AI Platform, an end-to-end platform for developing, deploying, and operating enterprise AI applications, C3 AI applications, a portfolio of industry-specific SaaS enterprise AI applications that enable the digital transformation of organizations globally, and C3 Generative AI, a suite of domain-specific generative AI offerings for the enterprise. This is an opportunity to shape the future of Agentic AI application development by creating intelligent systems and frameworks that enhance how engineers build, test, and ship applications.
NewSenior Manager, Clinical Vendor Contracts & Alliance Management, Clinical Operations Agios PharmaceuticalsSenior Manager, Clinical Vendor Contracts & Alliance Management, Clinical OperationsSan Francisco, CA$131,000–$196,000 / yearThe Senior Manager, Clinical Vendor Contracts and Alliance Management is responsible for relationship management, strategic insight, tactical support and execution of end-to-end outsourcing activities required to successfully execute clinical studies in a fast-paced and dynamic environment. Includes, but is not limited to contributing to service needs discussions in Clinical Trial Working Group (CTWG), identifying vendors, gathering business needs, and leading RFPs, bid defense meetings, scoring and award discussions.
NewFACILITIES & BUSINESS OPERATIONS MANAGER Rafiki CoalitionFACILITIES & BUSINESS OPERATIONS MANAGERSan Francisco, CA$70,000–$85,000 / yearThe Facilities & Business Operations Manager is responsible for leading and overseeing organizational operations, driving workflow improvements, managing facilities and IT coordination, and ensuring the organization's sites function efficiently and consistently. The Facilities & Business Operations Manager is a decision-maker, systems builder, and cross-departmental leader responsible for solving problems, improving processes, and ensuring operational efficiency and consistency across all Rafiki locations.
External Quality Assurance Lead Oklo IncExternal Quality Assurance LeadSanta Clara, CA$120,000–$140,000 / yearOklo Inc. is developing fast fission power plants to deliver clean, reliable, and affordable energy at scale; establishing a domestic supply chain for critical radioisotopes; and advancing nuclear fuel recycling to convert nuclear waste into clean energy. Oklo was the first to receive a site use permit from the U.S. Department of Energy for a commercial advanced fission plant, was awarded fuel material from Idaho National Laboratory, and submitted the first custom combined license application for an advanced reactor to the U.S. Nuclear Regulatory Commission.
Product & Quality Assurance Lead Momentus IncProduct & Quality Assurance LeadSan Jose, CA$150,000–$175,000 / yearThe Product & Quality Assurance Lead is responsible for developing, implementing, and maintaining the company''s Quality Management System (QMS), Product Assurance, Reliability, and Mission Assurance programs to ensure the successful delivery of safe, reliable, and compliant aerospace and spaceflight products. The successful candidate will be a hands-on leader with deep aerospace quality experience, capable of building scalable quality systems while partnering closely with Engineering, Operations, Supply Chain, and Program Management.
QA Lead (SDET) Vimo, Inc.QA Lead (SDET)Mountain View, CA$140,000–$170,000 / yearOur innovative approach to health insurance shopping and enrollment has expanded beyond exchanges, and we are now reinventing how states administer safety net programs such as Medicaid, SNAP (food stamps), child care, and unemployment insurance. Support and collaborate with client test teams to ensure successful and timely completion of User Acceptance Testing (UAT) and other processes leading up to the release.
Hospice QA Lead (RN) – Clinical Compliance & Chart Review Health LinkHospice QA Lead (RN) – Clinical Compliance & Chart ReviewSan Francisco, CaliforniaIn hospice, the care we provide matters deeply—and the way we document that care ensures patients receive the support they need. We are seeking a Hospice QA Lead based in our San Francisco office, focused on chart review, documentation accuracy, and regulatory compliance.
QA Lead, Robotics Dyna RoboticsQA Lead, RoboticsRedwood City, CaliforniaTesting Tools: Deep experience in developing and managing automated testing frameworks; familiarity with modern AI/ML testing, model evaluation, and regression benchmarking techniques; simulation (Gazebo, MuJoCo), and CI/CD tools (Docker, Kubernetes). Define and track key metrics (task success rate, cycle time, generalization across environments), build automated regression benchmarks, and gate releases on evaluation results to prevent regressions from reaching production.
NewQA Automation Architect/Lead with Health Cloud experience NeoDym TechnologiesQA Automation Architect/Lead with Health Cloud experienceSan Francisco, CAWe are looking for a strong QA Automation Architect/Leadwith expertise in automation and integrations, along with strong leadership capabilities in conflict resolution, coaching, and mentorship. Lead QA strategy, planning, Own end-to-end testing lifecycle including functional, integration, and regression testing.
NewQA Engineering Lead Meta Platforms IncQA Engineering LeadBurlingame, CABuild a test-driven engineering environment that drives improvements in quality Implement process changes to scale testing efforts across multiple products Plan, develop, and execute test coverage for multiple platforms Identify, test, track, and report KPI trends over the course of projects Diagnose issues, report defects, and propose regression tests to discover reoccurrences Work with engineers and project leads to triage and prioritize issues for resolution Own the process of creating metrics to measure and monitor product performance Partner with Automation and Infrastructure team to leverage automation to allow better reliability and scalability Analyze complex data, feedback, and user sentiment to identify improvements to products and software Funnel learnings back to development teams in a consistent and digestible manner to continuously improve productsBachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience 8+ years of experience driving Quality Assurance (QA) strategy and/or equivalent experience Experience working with Python, PHP, Java, C/C++ or equivalent language Experience debugging applications on Platform, PC, and Mobile components Experience building, shipping, and maintaining commercial software on top of consumer electronic devices Experience with test planning, test designing, and execution, and performance and stress testing Experience partnering and/or collaborating across multiple teams up to the leadership level Experience in managing black box and white box testing Experience in quality assurance within the virtual reality domain Experience establishing and maintaining quality processes such as test plans, defect tracking workflows, and release readiness criteria across product linesMeta builds technologies that help people connect, find communities, and grow businesses. As a QA Lead, you will ensure the delivery of high-quality software and platforms for wearables product lines, working alongside expert software engineers and research scientists to create technology that makes wearables pervasive and universal.
QA Analyst III BC ForwardQA Analyst IIIMenlo Park, CAFull timeThe ideal candidate will have strong experience in manual and automated testing, test planning, and quality metrics and a proven ability to drive test execution, triage defects, and support release readiness for small to medium-sized initiatives. BCforward is a leading global IT consulting and workforce solutions firm providing services and support to Fortune 500 and government clients.
Lead Quality Assurance Engineer (Multiple Positions) Beijing ByteDance Technology Co LtdLead Quality Assurance Engineer (Multiple Positions)San Jose, CA$201,053–$324,000 / yearOf the required experience, must have 3 years of experience in each of the following: Designing, developing, and maintaining automated testing frameworks and scripts integrated with CI/CD systems, and building robust, scalable, and high-quality test automation solutions for functional and regression testing; Reviewing requirements, specifications, and technical design documents to create systematic and comprehensive test plans and test cases, including estimating, prioritizing, planning, and coordinating testing efforts across team members; Creating and supporting REST-based API automation testing frameworks using Python; Building and testing software solutions using Agile methodology and DevOps development practices; Building automated test scripts using Java or Python for front-end testing, backend API testing, and ETL data automation; and Identifying, recording, resolving, and documenting software bugs, including tracking bugs and test metrics. Qualifications Must have a Master's degree or foreign equivalent degree in Computer Science, Engineering (any), Information Technology, or a related field, and 3 years of related work experience; OR a Bachelor's degree or foreign equivalent degree in Computer Science, Engineering (any), Information Technology, or a related field, and 5 years of post-bachelor's, progressive related work experience.
Quality Assurance - QA Analyst II Artech LLCQuality Assurance - QA Analyst IIMenlo Park, CA$46.66–$52.66 / hourAs a key player in ensuring product quality, you will execute and improve test processes, collaborate with engineering and QA leads, and support the delivery of high-quality features. This role is designed for individuals who can operate independently, contribute to test strategy, and take ownership of execution within defined scopes.
Executive Director, GCP QA Good Clinical Practice, Quality Assurance Revolution Medicines IncExecutive Director, GCP QA Good Clinical Practice, Quality AssuranceRedwood City, CA$265,000–$331,000 / 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. Minimum of 15 years of experience in the pharmaceutical or biotechnology industry, including at least 10 years in GCP QA or clinical quality leadership roles, with demonstrated experience leading and hosting regulatory inspections (e.g., FDA BIMO, EMA, MHRA, PMDA).
Executive Director, GCP QA (Good Clinical Practice, Quality Assurance) Revolution MedicinesExecutive Director, GCP QA (Good Clinical Practice, Quality Assurance)Redwood 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. Minimum of 15 years of experience in the pharmaceutical or biotechnology industry, including at least 10 years in GCP QA or clinical quality leadership roles, with demonstrated experience leading and hosting regulatory inspections (e.g., FDA BIMO, EMA, MHRA, PMDA).
Need - QA Analyst II in Menlo Park, CA Pride Technologies LLCNeed - QA Analyst II in Menlo Park, CAMenlo Park, CA$50–$55 / hourOnly applicable for San Francisco Candidates: Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of lactation accommodation rights, and this notice will automatically be given upon hiring, any inquiry of parental leave or lactation accommodation. Run and lead innovative testing techniques like benchmarking testing, battery testing, Requirements: Must-Have Skills.
Need - QA Analyst II in Menlo Park, CA Pride GlobalNeed - QA Analyst II in Menlo Park, CAMenlo Park, CA$50–$55 / hourOnly applicable for San Francisco Candidates: Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of lactation accommodation rights, and this notice will automatically be given upon hiring, any inquiry of parental leave or lactation accommodation. Run and lead innovative testing techniques like benchmarking testing, battery testing, Requirements:
QA Engineer Manpower EngineeringQA EngineerFoster City, CATemporaryManpowerGroup® (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.
Senior QA Manager Palo Alto Networks IncSenior QA ManagerSanta Clara, CA$185,000–$298,000 / yearTeam Upskilling: Act as a mentor and change agent, designing training pathways to help traditional manual and automation QA engineers transition into AI-augmented testing roles. For candidates who receive an offer at the posted level, the starting base salary (for non-sales roles) or base salary + commission target (for sales/com-missioned roles) is expected to be the annual range listed below.
QA - SDET MindSourceQA - SDETSunnyvale, CAThe ideal candidate will be responsible for developing tools, enhancing automation frameworks, executing and maintaining automation scripts, and collaborating closely with QA Leads and development teams. Experience with Content Management Systems (CMS), Digital Asset Management systems, and scalable dynamic rendering engines is highly preferred.
Senior Director of Technical QA (GMP) Summit TherapeuticsSenior Director of Technical QA (GMP)Palo Alto, CaliforniaHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. The Senior Director QA will report to the Vice President, Quality Assurance and Regulatory CMC, and provide comprehensive GMP quality oversight across the full chemistry, manufacturing, and controls (CMC) lifecycle for Summit’s oncology pipeline.
Traveling Quality Assurance - Quality Control Manager - MSG - Pharmaceutical Turner Construction CoTraveling Quality Assurance - Quality Control Manager - MSG - PharmaceuticalSan Francisco, CA$120,000–$217,000 / yearDevelop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples, documentation and tracking of potential cost changes, documentation and tracking of approved change orders within budgetary requirements. Position Description: Responsible for planning, coordinating and developing the project-specific Quality Assurance/Quality Control (QA/QC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents.
Quality Assurance Specialist Critical Mass IncQuality Assurance SpecialistSan Jose, CAThis role works closely with the QA Lead, developers, designers, project managers, and other QA team members to ensure high-quality digital experiences across platforms and devices. As part of a hybrid QA team, you will contribute to both manual testing efforts and automation initiatives, supporting the continuous improvement of quality processes across projects.
Senior Director of Technical QA GMP Summit Therapeutics IncSenior Director of Technical QA GMPPalo Alto, CA$217,000–$271,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. Overview of Role: The Senior Director QA will report to the Vice President, Quality Assurance and Regulatory CMC, and provide comprehensive GMP quality oversight across the full chemistry, manufacturing, and controls (CMC) lifecycle for Summit's oncology pipeline.
QRM Support Manager - National Tax Quality Assurance (NTQA), Quality Risk Deloitte Touche Tohmatsu LtdQRM Support Manager - National Tax Quality Assurance (NTQA), Quality RiskCA$93,000–$191,000 / yearOur team supports client-facing teams in how they approach the marketplace, develop service offerings, evaluate and onboard prospective clients, contract for services, deliver quality client service, and fulfill post-engagement and other recurring obligations. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.
Senior Program Manager, Quality Assurance Maplebear IncSenior Program Manager, Quality AssuranceCARemote$147,000–$155,000 / yearWe operate the feedback loop that turns support interactions into measurable improvements across the business: we evaluate quality across every channel, analyze trends and outliers to provide early warning, and route every signal to a named owner across five action workstreams (performance management, learning and development, automation, process, and product feedback). Collaboration on Roadmaps: Work with QA leadership, Product, Data Science, and cross-functional Analytics teams to understand quality trends, prioritize roadmap initiatives, and shape the future of AI-assisted auditing, rubric evolution, and contact-prevention work.
Senior Technical Program Manager, QA & Developer Experience Hp IqSenior Technical Program Manager, QA & Developer ExperienceSan Francisco, CaliforniaWe create breakthrough solutions that make complex tasks feel effortless, teamwork more natural, and ideas more impactful—always with a human-centric mindset. We’re assembling a diverse, world-class team—engineers, designers, researchers, and product minds—focused on creating an intelligent ecosystem across HP’s portfolio.
Manager, Quality Assurance, Compliance Vaxcyte IncManager, Quality Assurance, ComplianceSan Carlos, CA$151,000–$176,000 / yearSummary: Vaxcyte is seeking a Manager, Quality Assurance, Compliance who is responsible for providing day-to-day operational oversight governance and strategic oversight of key Quality System processes, with a primary focus on leading Change Control governance and deviation/investigation oversight review board leadership. The Manager acts as an operational backbone a governance leader for cross-functional quality processes, proactively identifying systemic risks, ensuring procedural compliance, driving performance through KPIs, and presenting quality system health and trends through Management Review.
Associate QA Operations Director - Labeling & Systems Exelixis IncAssociate QA Operations Director - Labeling & SystemsAlameda, CA$176,000–$250,500 / yearThe Associate QA Operations Director - Labeling & Systems is accountable for providing QA lead support for Quality Systems (Deviations, Change Control, CAPA, etc.), As a Partner responsible for guiding the organization in the successful, thorough, and timely execution of complex Quality Events (Deviations, Change Requests, CAPA's, CAPA Actions, Change Actions, Effectiveness Checks, etc.). BS/BA degree in Biology, Computer Science, Education, Learning & Development, Sciences, or related discipline and 11 years of related experience; or, MS/MA degree in Biology, Computer Science, Education, Learning & Development, Sciences, or related discipline and 9 years of related experience; or, Equivalent combination of education and experience.
NewQA CSV Contractor Katalyst Healthcares & Life SciencesQA CSV ContractorSan Francisco, CAOur client, a growing biotech research organization, is seeking a QA Computer System Validation (CSV) Contractor to support the Quality organization with computer system validation activities, primarily focused on clinical GxP systems. The ideal candidate has extensive experience in QA CSV within the clinical biotech/pharmaceutical industry and can work effectively in a fast-paced, cross-functional environment.
Senior Quality Assurance Engineer Hp IqSenior Quality Assurance EngineerSan Francisco, CaliforniaWe’re assembling a diverse, world-class team—engineers, designers, researchers, and product minds—focused on creating an intelligent ecosystem across HP’s portfolio. We create breakthrough solutions that make complex tasks feel effortless, teamwork more natural, and ideas more impactful—always with a human-centric mindset.
QA Automation Engineer Ebates Performance Marketing IncQA Automation EngineerSan Mateo, CA$96,442.50–$163,680 / yearHeadquartered in San Mateo, California with more than 4,000 employees worldwide, the Rakuten International business portfolio includes market leaders in e-commerce, digital marketing, advertising, communications and entertainment. As a leading shopping platform, Rakuten partners with thousands of top brands across apparel, beauty and wellness, grocery, travel, on-demand services, subscriptions, and dining, helping members save on everyday purchases.
NewQA CSV Contractor Karwell TechnologiesQA CSV ContractorSan Francisco, CAJob Summary: Our client, a growing biotech research organization, is seeking a QA Computer System Validation (CSV) Contractor to support the Quality organization with computer system validation activities, primarily focused on clinical GxP systems. The ideal candidate has extensive experience in QA CSV within the clinical biotech/pharmaceutical industry and can work effectively in a fast-paced, cross-functional environment.
SDET- QA Manger Tata Consultancy Services LtdSDET- QA MangerOakland, CA$100,000–$110,000 / yearResponsibilities: Defined and executed test strategies, test plans, and comprehensive test cases for end-to-end integration of eCommerce platforms, HighJump WMS with Microsoft D365 ERP and ensuring full coverage of material flow processes (Purchase Orders, Receiving, Staging, Inventory Management, Picking, Packing, Shipping) with strong focus on data validation and synchronization. Led functional, integration, regression, performance, API/services, and UAT testing cycles while managing the full defect lifecycle in Jira/Zephyr and including root cause analysis using AWS CloudWatch and Datadog logs, reproduction in QA environments, and verification of fixes.
Manager, Quality Assurance, Compliance VaxcyteManager, Quality Assurance, ComplianceSan Carlos, California$151,000–$176,000 / yearVaxcyte is seeking a Manager, Quality Assurance, Compliance who is responsible for providing day-to-day operational oversightgovernance and strategic oversight of key Quality System processes, with a primary focus on leading Change Control governance and deviation/investigation oversightreview board leadership. The Manager acts as an operational backbonea governance leader for cross-functional quality processes, proactively identifying systemic risks, ensuring procedural compliance, driving performance through KPIs, and presenting quality system health and trends through Management Review.
NewAssociate Director / Senior Manager, Quality Assurance AllakosAssociate Director / Senior Manager, Quality AssuranceRedwood City, CaliforniaAssociate Director / Senior Manager, Quality Assurance Allakos Inc. is a clinical-stage company developing therapeutic antibodies for inhibitory receptors on the surface of immune effector cells involved in allergic, inflammatory and proliferative diseases. Position Summary: As a member of the Allakos team you will be responsible for quality oversight activities related to Method Validation, Release testing, and Stability for Drug Substance and Drug Product.
QA Engineer Pyramid, IncQA EngineerSunnyvale, CAFull timePlease review the job description below: Job ID: 18-01270 Key Responsibilities:/Key Requirements and Technology Experience: • Review the process of new Bought-Out Parts (BOP) with the support and the co-operation of the Advanced Supplier Quality (ASQ) Engineer and/or the Program Quality Engineer. • Approve Production Part Approval Process (PPAP), only after acceptance by the Program Quality Engineer and the plant quality department.
PCBA Quality Assurance ManpowerPCBA Quality AssuranceHayward, CA$30–$34 / hourFull timeManpowerGroup® (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.
Vice President, Regulatory Affairs, Quality Assurance & Quality Control Venus Concept IncVice President, Regulatory Affairs, Quality Assurance & Quality ControlCA$200,000–$225,000 / yearWe have an exciting opportunity for a highly experienced, strategic, and performance driven Vice President, Regulatory Affairs, Quality Assurance & Quality Control to join our senior leadership team. The successful candidate will be a seasoned executive who has operated at a Vice President level for a minimum of 3 years, with demonstrated experience leading global, regulated medical device organizations.
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.