QA Engineer

• Creating and effectively executing test planning, manual test case authoring, scripting of automated tests, test execution, defect management, testing metrics and reporting, and other quality artifacts on projects and deliverables
• Identifying, investigating, and thoroughly documenting software defects and non-conforming software and performing comprehensive regression tests when defects have been resolved
• Providing prioritized issues list to management
• Participating in project reviews, risk assessments, retrospectives, sprint and backlog grooming sessions, and test case reviews
• Keeping abreast of industry test tools and QA skills, testing approaches, firm technology systems and applications, and technologies to proactively and continually contribute to improving the processes and quality of the firm’s systems
• Protecting and maintaining any highly sensitive, confidential, privileged, financial, and/or proprietary information that Latham & Watkins retains

Quality Assurance Analyst II

• Design, develop, and execute advanced test suites.
• Implement and execute test strategies across supported platforms and languages.
• Perform functional and automated testing.
• Develop backend integration tests and RESTful API tests.
• Build automation frameworks and test cases using Selenium and Python.
• Design integration, regression, and stress tests.
• Leverage AI tools to improve testing efficiency.
• Collaborate with Software Engineers and Program Managers to define test cases.
• Create and maintain test plans, specifications, and test suites.
• Provide technical leadership and promote engineering best practices.

Senior QA Engineer – Relocation Opportunity, USA

• Responsible for the leadership and operational execution of the site quality assurance function regarding the distribution and manufacturing (secondary packaging & labelling) activities.
• Oversee and drive day-to-day site operations, driving compliance to regulatory Good Manufacturing and Distribution Practice standards and operational improvements.
• Act as a primary expert and interface between supply chain and logistics, project management and other departments to drive delivery of client solutions with respects to Post Approval Named Patient/Expanded Access Program and Clinical Trial supply service lines for the site.

Senior Clinical Quality Assurance Associate

• Build and manage automated software testing suites of genomic algorithms (25%).
• Create or assist in creating, socializing, and presenting test approach, test artifacts, testing process, test metrics with appropriate teams (20%)
• Participate in and/or lead test case reviews, user stories, risk assessments, requirement reviews, sprint reviews, backlog grooming sessions (15%).
• Document and execute company software quality plans and reports (15%).
• Produce efficient test procedures, document results clearly, and provide effective communication throughout the software development life cycle (10%).
• Adopt new technologies for automation, software testing, genomic statistical analyses (10%).
• Other duties as assigned (5%).

Software Quality Engineer II

• Develop, implement, and provide ongoing quality assurance calibration of processes as well as a case management mentoring, both managed and delivered at the operational level
• Educate and equip operations with performance measurement and reporting tools that can be used to objectively measure and grow operations
• Provide national account and regulatory quality oversight
• As applicable, provide oversight and management of URAC compliance and renewals
• Work with executive, general and case management department management to ensure the case management department successfully implemented and is adhering to CorVel standards (including quality assurance, reporting, and management processes)
• Work closely with new hires to ensure consistent and full integration/training of all case management managers to CorVel standards as well as training for system usage pertaining to case management and reporting
• Identify developmental needs and and participate in training of case management leadership, including the training/re-training of all offices on standards and procedures, and usages of the CorVel case management and reporting system
• Develop, run and interpret management reports to ensure the case management operations are utilizing the tools available to manage compliance of services delivery within company standards
• Facilitate peer-to-peer quality reviews to ensure delivery of quality case management
• Review results and outcomes with general management and case management leadership and develop action plans where warranted
• Make recommendations in collaboration with field operations to ensure actions toward improvement are identified
• Develop and oversee case management manager mentor program to facilitate the onboarding of new supervision and management to equip field with the tools for compliance and consistency of CorVel standards and procedures
• Implementation, oversight and communication of regulatory requirements within case management services to include, state, federal and URAC
• Identify trends and recommend action plans to management for continuous process improvement
• Ability to travel up to fifty percent of the time

Quality Assurance Nurse

• Lead strategic air permitting and compliance programs for high-profile industrial clients.
• Serve as a trusted advisor, helping clients maintain operational flexibility while meeting regulatory requirements.
• Drive business growth by building strong client relationships and expanding ERM’s market presence.
• Mentor and develop project teams across multiple offices, fostering technical excellence and collaboration.
• Contribute to ERM’s national Air Quality technical community, sharing best practices and shaping industry standards.

Managing Consultant, Environmental Air Quality Compliance

• Design, implement, and maintain test automation frameworks across web, API, and mobile products, using CORTO's existing tooling and contributing to shared team repositories and goals
• Pick up and progress testing left outstanding at the end of the AU team's day or week, providing continuity across time zones
• Contribute to up-skilling team members through workshops, training, and paired programming sessions, in remote-friendly formats
• Perform code reviews to ensure compliance with established test frameworks
• Execute regression, smoke, and exploratory test cycles across the products
• Take an active role in QE process improvements, helping increase quality and efficiency in AI application delivery
• Work closely with developers and DevOps to support CI/CD pipelines and quality gates
• Communicate clearly and proactively across regions and time zones, keeping AU and US stakeholders aligned

Senior Quality Engineer

• Play a critical role in supporting quality assurance and compliance efforts across the Primrose system
• Serve as an operational partner to the Director of Quality Assurance & Compliance
• Monitor, track, document, and resolve issues impacting health, safety, licensing, and brand standards
• Ensure concerns are addressed promptly and compliance-related processes are executed consistently and effectively
• Monitor incoming concerns, online reviews, and operational requests, ensuring timely review, prioritization, and appropriate escalation
• Partner with internal teams and field support to coordinate responses, follow-up actions, and resolution of concerns
• Manage cases through investigation, documentation, follow-up, and resolution while maintaining accurate records of actions and outcomes
• Communicate case updates and key information to stakeholders and elevate emerging trends or recurring issues as appropriate
• Support the Issues Management process through intake, fact gathering, documentation, and coordination of compliance-related matters
• Coordinate escalation of significant issues to the Issue Response Team, ensuring information is complete, accurate, and appropriately documented
• Monitor open issues, track status updates, and follow up with stakeholders to support timely resolution and accountability
• Assist with the development and distribution of compliance-related communications and notifications in partnership with internal stakeholders
• Maintain organized, audit-ready records and documentation related to compliance, issue management, and quality assurance activities
• Utilize company systems to enter, update, and manage compliance-related data, ensuring accuracy, consistency, and completeness
• Generate routine and ad hoc reports that provide visibility into trends, risks, issue status, and resolution timelines
• Support the continuous improvement of tools, templates, workflows, resources, and training materials that strengthen quality assurance, safety, and brand standards
• Collaborate with cross-functional teams to support issue resolution, process improvement, and system-wide quality initiatives

Quality Assurance Specialist

• Lead supplier capability development initiatives to improve quality, scalability, robustness, and long-term supplier readiness
• Develop supplier improvement roadmaps and long-term development plans aligned with Strategic Procurement strategies and Technical Engineering priorities
• Own supplier improvement activities including Kaizens, process optimization efforts, and cost reduction initiatives
• Perform supplier capability assessments and technical evaluations
• Support and execute on make versus buy analysis
• Partner with Strategic Procurement to support category strategy and diversification efforts
• New supplier identification, qualification, and development initiatives
• Supply risk reduction initiatives and inspection programs
• Evaluation of outsource programs
• Support complex supplier programs including large qualifications, supplier expansion activities, and supplier capability growth efforts
• Lead supplier stabilization and monitoring activities for new suppliers, outsourced processes, or developing supply chains
• Support supplier segmentation and risk stratification activities associated with capability, capacity, scalability, and other business continuity factors
• Participate in subtier supplier assessments and mitigation efforts, as appropriate
• Contribute technical inputs supporting long-term supply continuity initiatives
• Lead and develop a growing Supplier Development Engineering team
• Provide technical guidance, mentorship, and prioritization support
• Help establish operating models, engagement processes, and best practices for the Supplier Development organization
• Partner across Procurement, Engineering, Manufacturing, Regulatory, and Quality functions

Supplier Quality Engineering Manager – Supplier Development

• Implement AI2IO’s software quality assurance framework, covering manual, automated, functional, and performance testing.
• Utilize Azure DevOps (ADO) for QA processes, including test plans, work item tracking, and reporting dashboards.
• Collaborate with developers, delivery leads, and analysts to embed QA early in the design and development lifecycle.
• Conduct hands-on testing, validation, and regression testing during initial phases of the QA program.
• Develop and maintain reusable test case libraries, templates, and documentation standards.
• Establish release readiness criteria, defect triage procedures, and metrics for quality tracking and reporting.
• Recommend and pilot test automation tools and frameworks for future scaling.
• Mentor development pods in QA best practices and support the recruitment and onboarding of future QA/Test Engineers.
• Continuously assess and improve QA workflows to reduce defects, rework, and time-to-release.

Senior QA Specialist

• Lead ongoing implementation and continuous improvement of the Software Quality Management System (QMS)
• Serve as the Quality Lead for the cybersecurity process
• Guide software development teams in creation and maintenance of Design and Development Files (DDFs)
• Support ISO 14971 risk management, IEC 62366 usability engineering, and FDA cybersecurity guidance integration into SDLC
• Support post-market cybersecurity surveillance activities
• Provide CAPA, complaints, audit, and QMS support related to software and cybersecurity incidents

Senior Quality Engineer, Cybersecurity

• Partner with Engineering throughout the development of new hardware, firmware, software, and connected products.
• Develop verification and validation strategies that ensure products meet customer, performance, and regulatory requirements.
• Design and execute test plans that validate functionality, reliability, usability, and safety.
• Build and evaluate prototypes while identifying opportunities to improve product quality before launch.
• Participate in design reviews and provide technical guidance throughout product development.
• Investigate failures, identify root causes, and drive corrective actions.
• Collaborate with global manufacturing partners to support successful product launches.

Senior Design Quality Engineer – Connected Products

• Ensure that products, processes, and systems meet internal quality standards and customer requirements
• Focus on validation planning, inspection control, metrology systems, and quality support
• Lead review and disposition of Non-Conforming Material Reports (NCMRs)
• Develop, review, and execute validation protocols such as IQ, OQ, and PQ
• Design and implement effective inspection strategies for materials and products
• Oversee calibration and maintenance of measurement and inspection equipment
• Act as the main point of contact for customer quality concerns and audits
• Ensure compliance with industry standards and participate in quality audits
• Collect, analyze, and present quality data; generate performance reports

Quality Engineer

• Lead and support analytical qualification, validation, and transfer of analytical methods for small and large molecules
• Review, approve and/or oversee various aspects of analytical validation activities
• Serves as the primary point of contact for Travere cross functional groups and contract vendors for analytical questions
• Provide subject matter expertise in aiding risk assessment activities
• Support product(s) stability program with review and approval of protocols
• Support the analytical review of data for regulatory submissions

Associate Director, Quality Assurance – Technical

• 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
• Leads validation efforts, projects, and action items including validations of: Process; Facilities, Utilities, Equipment (FUE); Shipping; Cleaning, Test Methods, and Computer System Validation
• Develop, execute, review, approve and/or oversee various aspects of a validation activities, including but not limited to: Master Plan (VMP) Validation Plan (VP) User Requirements Specifications (URS) Process Failure Mode and Effects Analysis (FMEA) of the process Process Characterization (PC) and Process Understanding (PU) studies Factory Acceptance Test (FAT) Site Acceptance Test (SAT) Commissioning Installation Qualification (IQ) Operational Qualification (OQ) Performance Qualification (PQ) Process Validation (PV) protocols/reports
• Direct Support of contract manufacturing, testing, storage and distribution organizations including, but not limited to: Change Control Deviations/Quality Events OOS/OOT investigations Corrective Actions and Preventive Actions Risk Management Vendor qualification and auditing Contractor qualification
• Collaborate closely with the Technical Operations Department for review and approval of CSP documentation for the above functionality
• Provide technical input to Travere Polices, SOPs, Work Instructions, etc., assuring internal needs are defined while complying with Regulatory requirements, Guidance and/or industry standards
• Review and approve Travere GxP related documents as requested
• Ensure compliance with applicable laws, regulations and guidelines for Travere Therapeutics’ contract manufacturing organizations
• Participate in the project core teams and sub-teams as needed and assigned
• Track progress versus timelines and goals

Director, Quality Assurance – Technical

• Participate in ongoing implementation of the Quality Management System (QMS) in conformance with US FDA QMSR, ISO 13485, IEC 62304, and IEC 62366-1 and other relevant standards.
• Support the product development team in creation of design history files (DHFs) including product requirements, software architecture and design specifications, design verification and validation test protocols and reports, risk management file, cybersecurity documentation, traceability matrices, etc.
• Guide and lead risk management activities, including failure modes and effects analysis (FMEA) and hazards analysis, in alignment with ISO 14971.
• Guide and lead computerized system assurance and validation activities for SW tools and systems.
• Engage and collaborate with suppliers and support design, development and design transfer activities.
• Support and participate in internal and external audits, coordinating and providing documentation and evidence of compliance.
• Support root cause analysis for nonconformances, defects and CAPAs, issue management, management review and quality data analysis.
• Foster a collaborative environment, champion continuous improvement initiatives and promote a quality culture across the organization.

Senior Software Quality Engineer

• Preparing and reviewing documentation in accordance with the bank's policies and procedures
• Working on highly complex documentation and supporting Loan Administrators
• Assisting the Market Leader in directing workflow and performing quality assurance
• Managing highly complex loan documentation while adhering to compliance and regulatory guidelines
• Reviewing loan documentation for accuracy and completeness
• Ensuring closing disclosure and loan document packages are prepared according to regulatory and client expectations

Document Administrator III – Custom Mortgage Lending, Inline Quality Assurance Specialist

• Supervise the activities of the QA Inspectors
• Responsible for labor budget management, performance evaluation, hiring, discipline, coaching, training and development
• Ensure that employees are trained and comply with safe work procedures
• Apply corrective actions when required and report all unsafe working conditions
• Investigate product/process failures quickly and thoroughly
• Manage relationships with intra- and inter-departmental colleagues and suppliers
• Administer all facilities’ hold, release and traceability programs
• Ensure timely release of equipment, ingredients and finished products
• Facilitate transitions between shifts for seamless handoffs

Assistant Manager – FSQA

• Ensuring company base aircraft are maintained in accordance with the Company Manual, FAR’s and Part 135 regulations.
• Conducts internal and vendor audits to ensure that proper qualifications are met to perform maintenance, inspection, and repair of company aircraft.
• Assists in CASS Program.
• Responsible for obtaining data used to measure the effectiveness of the maintenance and inspection program.
• Monitors corrective action measures determined by CASS committee.
• Monitor compliance with FAR’s, company policies and procedures.
• Monitor compliance with Airworthiness Directives, Service Bulletins and Manufacturer’s recommendations.
• Audit return to service paperwork, and maintenance tracking updates.
• Audit aircraft maintenance, inspection and repair for correct work scope, qualified personnel, proper tooling and appropriate equipment.
• Monitor procurement policies to assure required certification of all parts and materials used in the maintenance of aircraft.
• Institute changes to maintenance and inspection procedures and methods as required.

Aviation Maintenance Quality Assurance Analyst

• At BKF, we’re not just growing—we’re thriving! As a dynamic multi-service consulting firm, we specialize in planning, engineering, surveying, and construction management.
• The Project Manager will be able to build a project portfolio and a staff of additional qualified environmental professionals.
• BKF is seeking a self-driven, results-oriented Environmental Project Manager to lead projects and support the expansion of our Environmental Planning Practice in California.
• The CEQA Lead will be responsible for client engagement, leadership, strategic planning, staff development and business development focused in one of our key markets within the BKF Planning team.
• Job duties include leading environmental compliance as a project manager, overseeing CEQA/NEPA document preparation and related technical studies, conducting environmental constraints and peer review of CEQA/NEPA documents.
• Coordinating complex environmental projects and/or multi-agency/multi-jurisdictional planning efforts.
• Serving as a technical consultant and advisor to elected officials, citizen groups, and other stakeholders related to planning policies/standards, issues, processes, procedures, zoning/rezoning issues, ordinance changes, and environmental regulations.

QA Engineer jobs in California

See all jobs on JobTailor