NewSenior Manager, Technology Risk Assurance bdo consultingSenior Manager, Technology Risk AssuranceSan Diego, CA$150,000–$205,000 / yearThe Assurance Senior Manager, Technology Risk Assurance is responsible for acting as an IT audit technical resource to clients, as well as internal stakeholders (Assurance teams), in the resolution of complex and high-level tasks associated with the audit process. Applies advanced knowledge and understanding of governing principles; applying these principles to client transactions; and documenting and communicating an understanding and application of these principles by: Plans and executes IT audits, including obtaining an understanding of the control environment, designs test plans, evaluates deficiencies, and assesses the overall financial reporting control environment.
Director, Commercial Risk Evaluation and Mitigation Strategies (REMS) Lead - Remote Agios PharmaceuticalsDirector, Commercial Risk Evaluation and Mitigation Strategies (REMS) Lead - RemoteSan Diego, 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.
NewSRS - Lead – RN - Pediatrics - Full Time - Day Shift SHARP HEALTHCARESRS - Lead – RN - Pediatrics - Full Time - Day ShiftLa Mesa, CA$90,000–$108,000 / yearThe actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant’s years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices. Demonstrates typing skills proficiency by: Using a keyboard, required to type proficiently and accurately; Have the ability to type a minimum of 30 words per minute with 0-2 errors; Have the ability to proof work.
Field Operations Supervisor Pacific Coast Cleaning, Inc.Field Operations SupervisorSan Diego, CA$70,000–$77,000 / yearManaging a field crew of 30 staff, this leader schedules, plans, prioritizes, allocates team members, and drives the completion and quality of construction cleaning projects. The key to success is the ability to plan, prioritize, and manage a mix of direct reports, projects, and customers in alignment with job profitability and quality expectations while also improving processes and simplifying operations.
QA Group Lead PCI Pharma ServicesQA Group LeadSan Diego, CA$36.54–$41.10 / hourSUMMARY: The QA Group Lead is responsible for performing a wide variety of semi-routine, moderate to highly complex activities pertaining to assuring compliance with applicable regulatory requirements, providing QA oversight of manufacturing operations, documentation and record management, facility and equipment management, change controls, investigations, and support of validation activities. ESSENTIAL JOB FUNCTIONS-OTHER DUTIES MAY BE ASSIGNED: Leads the review and approval of executed technical documentation in support of the manufacture and testing of Drug Substance and Drug product.
Associate Director, Clinical Quality Assurance Artiva Biotherapeutics IncAssociate Director, Clinical Quality AssuranceSan Diego, CA$172,000–$195,000 / yearKnowledge and hands on experience in regulatory inspections, clinical investigator site/vendor/internal audits Thorough knowledge of current Good Clinical Practices and Good Clinical Laboratory Practices as they relate to all phases of cell therapy product human clinical trials. In this role, you will design and execute risk-based GCP quality oversight strategies, lead investigations of significant compliance events, and plan and conduct routine and for-cause audits of clinical investigator sites, CROs, and vendors.
Sr. Manager, QA Aspen Neuroscience IncSr. Manager, QASan Diego, CA$160,000–$186,000 / yearTotal Rewards and Culture: Aspen Neuroscience, Inc., located in scenic Torrey Pines, is noted for its collaborative and learning focused culture where each person is valued for contributing their strengths and energy to building a world-class line of products for patients in need. SUMMARY: The Senior Manager, Quality Assurance leads the execution, maintenance, and ongoing improvement of GxP quality systems and teams that support Phase 2a through Phase 3 clinical and manufacturing operations.
Sr. Manager, Clinical Quality Assurance Artiva Biotherapeutics IncSr. Manager, Clinical Quality AssuranceSan Diego, CA$150,000–$172,000 / yearKnowledge and hands on experience in regulatory inspections, clinical investigator site/vendor/internal audits Thorough knowledge of current Good Clinical Practices as they relate to all phases of cell therapy product human clinical trials. As Senior Manager, Clinical QA, youll lead risk-based GCP oversight across our clinical programs - driving audits, investigations, and inspection readiness that protect patients and data integrity from first-in-human through approval.
Director, Quality Assurance & Quality Systems Capricor TherapeuticsDirector, Quality Assurance & Quality SystemsSan Diego, CaliforniaCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without express written approval from Talent Acquisition and a fully executed agreement with Capricor. The role advances the company's Quality Management System, drives inspection readiness, and ensures quality processes are scalable, compliant, and aligned with late-stage development and commercial launch.
Sr. Manager, QA Aspen NeuroscienceSr. Manager, QASan Diego, California$160,000–$186,000Manage and continuously improve multiple QA functional areas, including document control, training systems, supplier quality, quality events (deviations, CAPA, change control, nonconformance), and batch disposition. Aspen Neuroscience, Inc., located in scenic Torrey Pines, is noted for its collaborative and learning focused culture where each person is valued for contributing their strengths and energy to building a world-class line of products for patients in need.
NewDirector, Quality Assurance & Quality Systems CapricorDirector, Quality Assurance & Quality SystemsSan Diego, CAThe ideal candidate brings hands‑on QA and Quality Systems experience, deep knowledge of GMP and FDA requirements, and a proven ability to partner cross‑functionally to build a proactive, risk‑based quality culture. The Director, Quality Assurance & Quality Systems will lead and support quality assurance and quality systems activities for Capricor's clinical and commercial‑stage biotechnology operations.
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 Director, Quality Assurance - Gene Therapy Insmed IncSenior Director, Quality Assurance - Gene TherapySan Diego, CA$214,000–$292,000 / yearFor New York City Residents: To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications. Deep knowledge of phase-appropriate quality systems, regulatory requirements (21 CFR Parts 210/211, 600s, 820, ICH, EU Annexes, ISO 13485/14971), and compliance expectations across clinical development.
Manager, QA Operations Maravai LifeSciences Holdings IncManager, QA OperationsSan Diego, CAWho we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world''s leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.
NewQuality Assurance and Training Supervisor MaximusQuality Assurance and Training SupervisorSan Diego, CAMaximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. This role is responsible for establishing and communicating QA performance targets, managing QA team performance, and ensuring the consistent delivery of highquality service through datadriven insights and continuous improvement.
Sr. Clinical QA Manager Neurocrine Biosciences IncSr. Clinical QA ManagerSan Diego, CA$148,500–$203,000 / yearThe company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. Your Contributions (include, but are not limited to): Good Clinical Practice ("GCP") Audit Management: Lead, plan, conduct, and oversee GCP audits (e.g., vendor, clinical investigator site, internal audits) to ensure compliance with applicable GCP/regulatory requirements and guidelines, study protocols, monitoring plans and applicable policies/procedures.
Supervisor Quality Assurance DexCom IncSupervisor Quality AssuranceSan Diego, CA$87,000–$145,000 / yearMeet the team: The Supervisor Quality Assurance manages a team of Quality Inspection personnel in the Receiving Inspection area in San Diego COGS department and a group of Quality Supports that coordinates and maintains material traceability of Nonconforming Material through the San Diego site. The supervisor organizes the tasks and requirements of the Receiving Inspection area in coordination with Logistics and Distribution management at Dexcom's SD inbound Materials warehouse and coordinates the tasks and work plans of the Non-Conforming Material (NCMR) area.
NewQuality Assurance Manager TriMas CorpQuality Assurance ManagerEl Cajon, CAProduce quality products to customer specification and ship customer orders on time, directs and administers quality assurance program designed by performing the following duties personally or through subordinates. Since 1968, Weldmac has combined heavy forming, CNC machining, advanced welding, and laser processing to solve large-scale fabrication challenges with repeatable precision.
Quality Assurance Manager Blue Marble CommunicationsQuality Assurance ManagerPoway, CAFull timeOur current product offerings include software-defined RF, microwave, and millimeter-wave modem/transceivers; optical laser communications terminals, Ethernet routers/switches, and systems comprised of combinations of these modules. Blue Marble Communications designs and manufactures high-performance RF, free-space optical, and network communications modules and systems for deployment onboard satellites and other space vehicles.
NewQuality Assurance Manager Voyager TechnologiesQuality Assurance ManagerSan Diego, CaliforniaThe Quality Assurance Manager for Voyager's San Diego space, defense, and national security hardware programs is responsible for leading site quality and mission assurance across multiple concurrent flight programs and serving as the AS9100D Management Representative for the site Quality Management System. Bachelor's degree in Quality, Industrial, Manufacturing, Mechanical, Electrical, or Aerospace Engineering with 7 years of experience in quality engineering or mission assurance, OR a Master's degree with 5 years of experience, OR 11 years of relevant experience in lieu of a degree.
NewSr Manager QA - Computer Systems Validation MRINetworkSr Manager QA - Computer Systems ValidationSan Diego, CAIdentify and track progress against key project milestones partnering with applicable business process, equipment, and facilities owners along with any external providers to ensure overall project success and compliance. The cross-functional role will work to drive continuous improvement across all GxP systems and equipment while serving as the primary point of contact for computer systems validation.
Quality Assurance Manager NANO Nuclear Energy IncQuality Assurance ManagerSan Diego, CAReporting directly to the Vice President of Operations, the QA Manager serves as the senior owner and accountable lead for the Quality Assurance Program, with sufficient independence and direct executive access to escalate safety or quality matters. Upon successfully demonstrating operational excellence, team leadership, and cultural fit through a defined due diligence period, the candidate will be eligible for a direct promotion to the Director of Quality Assurance (DQA) title.
QA Complaint Intake Specialist RD PartnersQA Complaint Intake SpecialistSan Diego, California£49,820–£62,400The individual should have a basic understanding of medical device and quality system requirements; strong organizational skills; strong attention to detail; ability to accurately review and document information; ability to determine the number of complaint events from emails and supporting communications; ability to identify missing or unclear information; ability to coordinate timely follow-up; good written, verbal, and interpersonal communication skills; ability to work professorially with cross-functionally teams, Complainant, Customer Support, Field Sales, Medical Affairs, QA, Operations, and Complaint Investigators; ability to manage multiple complaint records within required timelines; and working knowledge of Microsoft Word, Excel, Outlook, and eQMS systems. Receive complaint information from approved intake sources including Customer Support, field personnel, sales representatives, Medical Affairs, email communications, phone calls, and other authorized channels.
Deputy Director - Employee Services and Quality Assurance - Public Utilities Dpt. - - 900 (UNC)) City of San Diego Public Utilities DepartmentDeputy Director - Employee Services and Quality Assurance - Public Utilities Dpt. - - 900 (UNC))San Diego, CADesired Qualifications: The ideal candidate will possess the following qualifications: Substantial, progressively responsible management experience, preferably with substantial City of San Diego experience in internal support services, human resources, finance, quality assurance, development and monitoring. Under the general direction of the Public Utilities Department Director and Business Support Branch Assistant Director, the ESQA Deputy Director oversees and manages critical functions associated with the water and sewer funds.
QA Associate III PCI Pharma ServicesQA Associate IIISan Diego, CA$29.65–$33.36 / hourSUMMARY: This position is responsible for performing a wide variety of routine and semi-routine activities pertaining to assuring compliance with applicable Quality Assurance (QA) and regulatory requirements, including assisting with audits, training programs, and documentation review in support of GMP operations. ESSENTIAL JOB FUNCTIONS-OTHER DUTIES MAY BE ASSIGNED: Assists in regular follow ups with end users to ensure timely completion of open investigations and investigation activities.
QA Associate III - Second Shift (2-10) PCI Pharma ServicesQA Associate III - Second Shift (2-10)San Diego, CaliforniaThis position is responsible for performing a wide variety of routine and semi-routine activities pertaining to assuring compliance with applicable Quality Assurance (QA) and regulatory requirements, including assisting with audits, training programs, and documentation review in support of GMP operations. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
Director, Quality Assurance Operations Avid Bioservices IncDirector, Quality Assurance OperationsSan Diego, CA$165,600–$207,000 / yearManaging People - Includes staff in planning, decision-making, facilitating and process improvement; Takes responsibility for subordinates' activities; Makes self available to staff; Provides regular performance feedback; Develops subordinates' skills and encourages growth; Solicits and applies customer feedback (internal and external); Fosters quality focus in others; Improves processes, products and services. Analytical/Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics.
AI and ML Platforms QA Engineer III ICW GroupAI and ML Platforms QA Engineer IIISan Diego, CA$95,378.98–$160,850.17 / yearHeadquartered in San Diego with regional offices located throughout the United States, ICW Group has been named for ten consecutive years as a Top 50 performing P&C organization offering the stability of a large, profitable and growing company combined with a focus on all things people. Partners with Data Scientists and ML Engineers to design and execute testing strategies for AI/ML applications and pipelines, including pipeline validation, data validation, feature and model validation, inference testing, integration and API testing.
QA Associate I - Second Shift (2-10) PCI Pharma ServicesQA Associate I - Second Shift (2-10)San Diego, CaliforniaThe Associate I performs documentation review and ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
QA Associate I PCI Pharma ServicesQA Associate ISan Diego, CA$21.69–$24.41 / hourThe Associate I performs documentation review and ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
Sr Software QA Engineering DexCom IncSr Software QA EngineeringSan Diego, CA$95,900–$159,900 / yearLead in the effective application, compliance, and continuous improvement of policies, procedures, and practices related to software development and validation across software teams, including: Drive Pre-market risk management deliverables like SHA, design FMEA and support Cyber security risk management. This position will interface with different cross functional groups (Software Engineering, Software Test, Regulatory Affairs, Marketing, Project managers, Systems Engineering, Cybersecurity, and others).
NewQuality Assurance Manager BLUEMARBLE COMMUNICATIONSQuality Assurance ManagerSan Diego, CAOur current product offerings include software-defined RF, microwave, and millimeter-wave modem/transceivers; optical laser communications terminals, Ethernet routers/switches, and systems comprised of combinations of these modules. Blue Marble Communications designs and manufactures high-performance RF, free-space optical, and network communications modules and systems for deployment onboard satellites and other space vehicles.
Coordinator, Quality Assurance RN, PACE Family Health Centers of San Diego IncCoordinator, Quality Assurance RN, PACESan Diego, CA$50–$61.86 / hourServices include, but are not limited to adult care, chronic disease management, pediatrics, comprehensive women's care including obstetrics, dental, vision, case management, physical rehabilitation, speech therapy for children, vaccinations, infectious diseases, behavioral health, substance use counseling and a host of specialty services including cardiology, podiatry, endocrinology, dermatology, among others. We operate more than 90 sites across San Diego County, including 29 primary care clinics, 23 behavioral health facilities, 10 physical rehabilitation clinics, nine dental clinics, five vision clinics, four outpatient substance use treatment programs, three mobile medical units, two mobile counseling centers, two urgent care centers, and a pharmacy.
Associate Director, Quality Assurance - Technical Travere Therapeutics IncAssociate Director, Quality Assurance - TechnicalSan Diego, CARemote$150,000–$195,000 / yearDemonstrated ability to critically assess/analyze information, draw the appropriate technical conclusions based upon system knowledge, influence approach, and work effectively across different internal and external functions to resolve complex technical quality issues. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community.
Director, Quality Assurance - Technical Travere Therapeutics IncDirector, Quality Assurance - TechnicalSan Diego, CARemote$189,000–$246,000 / yearResponsibilities: Lead, manage and perform critical Quality Assurance (QA) GMP functions providing oversight of GMP Contract Service Providers (CSPs) for Drug Substance and Drug Product activities/projects leading up to Phase 3 Process Validation and Commercialization. Compensation: Our competitive compensation package includes a combination of both cash compensation (base pay and short-term incentive) and long-term incentive compensation (company stock), designed to recognize, retain, and reward employees.
Director, Clinical QA Neurocrine Biosciences IncDirector, Clinical QASan Diego, CA$181,800–$248,000 / yearThe company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients with Prader-Willi syndrome, endometriosis and uterine fibroids , as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. Responsible for building and leading a team of highly trained and skilled quality managers, specialists and associates in order to implement the quality systems and perform activities necessary to ensure compliance and to ensure QA support of clinical study teams.
Swift QA Engineer Pride Technologies LLCSwift QA EngineerSan Diego, CA$75–$80 / hourExperience building evaluation harnesses for AI features: authoring golden-question datasets and CSV fixtures, scoring model outputs with deterministic matchers and LLM-as-judge rubrics (correctness, hallucination, concision), and tracking evaluation-score regressions across commits. Preferred Qualifications: Practical experience with Swift and test frameworks, Swift Testing (@Test/@Suite/#expect) and XCUITest, building UI automation with stable accessibility identifiers and dependency-injected test seams.
NewQuality Assurance Specialist Pacific Health GroupQuality Assurance SpecialistSan Diego, CA$27–$33 / hourOur Core ValuesSpeak with integrity—clear, respectful, and honest in every interactionEmbrace innovation, trying new ideas, learning fast, and improving careOwn our roles, staying accountable for outcomes and documenting accuratelyBuild genuine connections with members, families, and teammates through empathy and cultural sensitivityLead with trust by being consistent, transparent, and following throughCelebrate wins together, recognizing individual and team achievementsCollaborate with purpose, partnering across departments and with community providers to solve problemsAsk for support and offer support, because thriving together is how we serve our members bestRole Overview & ImpactThe Quality Assurance Specialist ensures quality, compliance, workflow accuracy, and performance excellence across Enhanced Care Management (ECM), Community Supports (CS), Behavioral Health (BH), and Community Health Worker (CHW) operations. The QA Specialist serves as the internal auditor, workflow analyst, and process‑improvement lead for all member‑facing activities, including assessments, referrals, documentation, disenrollment workflows, re‑engagement processes, outreach, verification, and communication functions.
Clinical - QA Associate, Clinical Studies Medvacon Life Sciences LLCClinical - QA Associate, Clinical StudiesSan Diego, CAAbility to work effectively under pressure to meet deadlines Physical Requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Ability to identify aberrant data and potential quality/compliance concerns escalating to management CSD-JD-QA Associate - Clinical Supplies v1.0.
Clinical - QA Associate, Clinical Studies Medvacon Life Sciences, LLCClinical - QA Associate, Clinical StudiesSan Diego, CAFull timeAbility to work effectively under pressure to meet deadlines Physical Requirements: • On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. • Ability to identify aberrant data and potential quality/compliance concerns escalating to management CSD-JD-QA Associate – Clinical Supplies v1.0.
QA Inspector Dwyer Instruments, Inc.QA InspectorSan Marcos, CA$20–$25 / hourWith more than 60 years of innovation and experience, FCI serves a wide range of industries including chemical, oil & gas, power and energy, water and wastewater, pharmaceutical, nuclear power, and aerospace, with products such as mass flow meters, flow switches, level switches, and sensors. About Fluid Components International, LLC: Fluid Components International (FCI) is a leading global manufacturer of advanced flow and level measurement instrumentation, utilizing patented thermal dispersion technologies to deliver highly accurate, reliable solutions for industrial process applications.
Associate Director, Clinical Quality Assurance Vera Therapeutics IncAssociate Director, Clinical Quality AssuranceSan Diego, CA$140,000–$210,000 / yearThe individual partners closely with Clinical Operations, Pharmacovigilance, Data Management, Regulatory Affairs, and other development function and serves as a key member of study teams, helping identify quality issues and risks, and reviews quality events, investigations, and CAPAs; analyzing quality signals across studies and vendors that support risk-based decision making, and ensuring quality management practices are appropriately implemented throughout the clinical trial lifecycle. Vera Therapeutics' lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis.
Prin QA Engineer General Dynamics CorpPrin QA EngineerSan Diego, CAGeneral Dynamics Ordnance and Tactical Systems (OTS) is a global leader in the design, engineering and production of munitions, energetics, weapons, armaments, and missile subsystems around the world. In addition to the benefits discussed above, the company offers the following voluntary benefits: Critical Illness Insurance, Accident Insurance, Identify Theft Protection, Enhanced Legal Services, Auto and Home Insurance, Pet Insurance, Commuter Benefits, Hospital Indemnity Insurance, Educational Assistance.
Swift QA Engineer Pride GlobalSwift QA EngineerSan Diego, CA$75–$80 / hourExperience building evaluation harnesses for AI features: authoring golden-question datasets and CSV fixtures, scoring model outputs with deterministic matchers and LLM-as-judge rubrics (correctness, hallucination, concision), and tracking evaluation-score regressions across commits. Preferred Qualifications: Practical experience with Swift and test frameworks, Swift Testing (@Test/@Suite/#expect) and XCUITest, building UI automation with stable accessibility identifiers and dependency-injected test seams.
Senior Associate, QA Compliance Artiva Biotherapeutics IncSenior Associate, QA ComplianceSan Diego, CAOur lead product candidate, AlloNK, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.
AI QA Automation Engineer GoFormz, Inc.AI QA Automation EngineerSan Diego, CA$70,000–$110,000 / yearIf you love working in a fast-paced and collaborative environment; have a passion for quality and cutting-edge AI testing tools; thrive on building robust automated systems and have a "can do" attitude - We want you! You will design AI-augmented test suites, maintain Playwright frameworks, and integrate AI tools to accelerate test generation and defect detection across web and mobile applications.
Senior Manual QA Engineer Faro Health IncSenior Manual QA EngineerCALeveraging your deep expertise in SaaS, cloud-native architectures, and LLM-augmented workflows, you will analyze complex user requirements, design comprehensive test strategies, prepare/execute test cases and serve as a mentor to junior and contractor engineers. Test Strategy & Design: Analyze user requirements and design documents to develop detailed, risk-based test plans and manual test cases for a complex SaaS platform.
Quality Assurance Associate II Capricor TherapeuticsQuality Assurance Associate IISan Diego, CaliforniaCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without express written approval from Talent Acquisition and a fully executed agreement with Capricor. At Capricor, you’ll join a collaborative environment where employees are encouraged to contribute, grow, and help build the systems, science, and operations needed to support our next stage of growth.
NewQA Operations Specialist II Maravai LifeSciences Holdings IncQA Operations Specialist IISan Diego, CA$60,000–$70,000 / yearWe are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world''s leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics.
Quality Assurance Director FIZE Medical IncQuality Assurance DirectorSan Diego, CAMaster's degree or equivalent in a relevant field, with 8+ years of experience in quality assurance/control, including leadership roles within the medical device or diagnostics industry. • Lead the preparation and management of external audits and implement corrective actions related to MDSAP, MDR, ISO, FDA, and other relevant regulatory bodies.