April 30, 2026For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com.
San Diego, California21 days ago
2. Rebuilding supplier quality oversight capabilities lost through attrition and organizational restructuring, which affected both the prior Supplier Quality Engineering group and Supply Chain Engineering roles. Ascential Medical and Life Sciences is a leader in delivering precision engineering and automation solutions for medical devices, diagnostics, and life sciences.
San Diego, CA30+ days ago
li style="margin-bottom:13px">Cross-Functional Collaboration: Interact daily with other functions such as technical support, engineering, facilities, production control, and finance to meet organizational goals Strategic Planning: Develop and implement strategic plans, including creating current and future state value stream maps. Trigo’s team of dedicated Delivery Assurance Specialists, Supplier Development Specialists, Supplier Quality Engineers and Program Managers support hundreds of Customers and are deployed to thousands of Suppliers worldwide focused on achieving On-Time and On-Quality Delivery results.
San Diego, CA30+ days ago
Trigo’s team of dedicated Delivery Assurance Specialists, Supplier Development Specialists, Supplier Quality Engineers and Program Managers support hundreds of Customers and are deployed to thousands of Suppliers worldwide focused on achieving On-Time and On-Quality Delivery results. - Prior practical experience and implementation of Quality Engineering tools and systems such as: DOE, FMEA, SPC, RCCA, APQP, PPAP, controls plans, material control, process control, systems performance, product evaluation, MSA, metrology, automated measurement, and software is preferred.
San Clemente, CA30+ days ago
p>Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. This person has primary responsibility for performing supplier/vendor assessments, on-site inspections, and monitoring performance of vendors/suppliers in accordance with the Supplier Quality Management program.
Aliso Viejo, CA30+ days ago
The Senior Quality Engineer I will be responsible for establishing documentation control and approval workflows to support manufacturing and testing for processes, test methods, test results, batch records, etc. for manufacturing and collaborate with Product Development, Manufacturing, and other cross-functional teams to ensure product quality and regulatory compliance. The Senior Quality Engineer I will support all RxSight products and will be expected to apply knowledge of process engineering, risk management, and quality engineering techniques to innovate and improve quality system processes while simultaneously ensuring conformance to applicable regulatory requirements.
San Diego, CA30+ days ago
p>POSITION SUMMARY: The Senior Quality Engineer performs key aspects required for proper evaluation and resolution of quality related matters and technical issues that may arise during manufacturing and maintenance of turbine engine components. This position supports activities related to quality system requirements compliance, and additionally creates, tracks, and provides statistical analysis, reports, and metrics for quality related activities.
San Diego, California30+ days ago
li>Assesses quality performance issues of assigned suppliers using multiple input data streams from Dexcom and the supplier’s process to drive / support supplier development activities. Some type of activities may include assisting with defining design inputs; designing components and processes; verifying that design outputs satisfy design inputs.
San Diego, CA30+ days ago
p>POSITION SUMMARY: The Quality Engineer performs key aspects required for proper evaluation and resolution of quality related matters and technical issues that may arise during manufacturing and maintenance of turbine engine components. This position supports activities related to quality system requirements compliance, and additionally creates, tracks, and provides statistical analysis, reports, and metrics for quality related activities.
p>We are seeking a Supplier Quality Engineer to drive product quality with the supply chain across the entire lifecycle - from new product introduction (NPI) through sustaining production - while ensuring AS9100 compliance, robust quality systems, and continuous improvement. Must have the analytical ability required to develop solutions to routine and non-routine quality issues and the skills required to present those solutions to internal contacts.
We are seeking an experienced Supplier Quality Engineer to drive product quality with the supply chain across the entire lifecycle - from new product introduction (NPI) through sustaining production - while ensuring AS9100 compliance, robust quality systems, and continuous improvement. Typically requires a bachelor''s or master''s degree in engineering or related discipline and five or more years of related experience with a bachelor''s degree or three or more years with a master''s degree.
Carlsbad, California7 days ago
For more information about Enovis, please visit
li>Review and approve Change Orders required by process owners to write and issue procedures to assure compliance with the current FDA QSR regulations, ISO 13485, CMDR and Medical Device Directive requirements; and to provide training to process owners related to Quality Management System requirements, as necessary.
Support Sustaining Design Quality Engineering Assignments, including ensuring verification and validation for design changes for product and process improvements, component end of life transition, and quality improvements.
p>While performing the duties of this job, the employee is frequently exposed to an office environment; and occasionally exposed to manufacturing environment and elements such as odor, noise, dust, heat, cold, chemicals, or some element present which makes conditions less desirable than usually found in an office. Work with other engineering groups as necessary (manufacturing, industrial, and process engineers) in order to implement corrective actions as necessary to prevent quality escapes and improve manufacturability parts and assemblies.
Familiarity with common medical device manufacturing and assembly technologies (e.g., molding, electronic assembly, surface-mount technology, joining and bonding methods, forming and machining operations, and product identification processes) is desirable, with the ability to understand how manufacturing capabilities and limitations may influence mechanical design decisions, tolerances, and risk controls; deep hands‑on manufacturing expertise is not required. The position drives robust Design Controls and Risk Management practices for complex electro-mechanical systems and consumables, while working independently to optimize and continuously improve quality system processes and internal operations to ensure conformance to specifications, effective risk reduction, and continuous improvement of both device quality and business performance.
p>For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). Activities involves assessing incoming inspection methods and sampling, process controls at the contract manufacturers, facilitating nonconforming material report investigation and closure, failure investigations, CAPA and SCAR ownership, and change control activities.
San Diego, CA30+ days ago
Champion activities to contribute and drive in the investigation and elimination of internal and external quality problems using applicable problem-solving techniques for determining Containment, Root Cause and Corrective/Preventive Action solutions along with Verification actions. About Us: AMETEK Programmable Power Business Unit (~$160M) is headquartered in San Diego, CA and provides the most advanced Power and Instrumentation solutions for Precision Stimulus, Process Power and Measurement and Switching applications.
San Diego, CA30+ days ago
AMETEK Programmable Power Business Unit (~$160M) is headquartered in San Diego, CA and provides the most advanced Power and Instrumentation solutions for Precision Stimulus, Process Power and Measurement and Switching applications. Demonstrate a high level of technical competence related to electronics and electromechanical box build product assembly manufacturing technology, focusing on consistent quality and reliability.
For specific work locations within San Jose, the San Francisco Bay area and New York City metropolitan area, the base pay range for this role is $79,500.00- $119,500.00/ annually. Learn more about Viasat's comprehensive benefit offerings that are focused on your holistic health and wellness at https://careers.viasat.com/benefits.
San Diego, CA30+ days ago
In this pivotal role, you will apply your technical expertise, analytical skills, and leadership capabilities to evaluate product complaints, mitigate risks, and collaborate across functions to deliver innovative solutions that uphold our commitment to womens health. Strong knowledge of post-market engineering practices, including reliability engineering, complaint trending, failure analysis, and returned product evaluations.
San Diego, CA30+ days ago
p>POSITION SUMMARY: Associate Quality Engineer aims to ensure that the product or service an organization provides is fit for purpose and meets both external and internal requirements, including legal compliance and customer expectations. We are a leading provider of aftermarket parts, repairs, and solutions that safely & reliably extend the life of aircraft engines and gas turbines.
p/>For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable).
- Support design controls activities for surgical instruments used with Informatix systems to ensure efficient, effective, and compliant new product launches including, but not limited to development planning, requirements specifications, verification and validation .
li>Lead design assurance and development activities, including engineering studies, feasibility testing, and drawing reviews for new product development. Highly Preferred knowledge of Software Development Life Cycle Processes (IEC 62304) and Usability Engineering Processes (IEC 62366).
Develop, improve, and implement quality methods and systems, working on cross functional teams in a regulated environment to ensure the safety, reliability and efficacy of products and processes. Lead Material Review Board (MRB), own Non-Conformance (NC) development and resolution, lead reworks and deviations, participate in Supplier Review Board (SRB).
San Diego, CA30+ days ago
You will be responsible for guiding teams through the execution of design control activities in alignment with quality system requirements and current best practices to ensure the company's products and processes are safe, effective, and meet customer performance needs. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package.
- Quality Engineer with experience in the Medical Device industry, specializing in quality engineering, design assurance, risk management, design controls, and product verification & validation. Roles & Responsibilities:
- Support quality engineering and design assurance activities within the Medical Device industry.
li>Must have strong leadership skills to direct staff members and ensure project costs and schedules are maintained while representing the organization on technical quality assurance issues. - Typically requires a bachelor''s or master''s degree in engineering or related discipline and six or more years of related experience with a bachelor''s degree or four or more years with a master''s degree.
div style="text-align:justify">Skill Descriptors:
- Effective Communications: Understanding of effective communication concepts, tools and techniques; ability to effectively transmit, receive, and accurately interpret ideas, information, and needs through the application of appropriate communication behaviors.
- Supplier Management - MFG: Knowledge of processes and methods to effectively manage business relationships and transactions with suppliers of raw materials or product components; ability to apply related knowledge, experience and skills into real practice.
San Diego, California26 days ago
div>Lead 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).
Prin QA Engineer General Dynamics Ordnance and Tactical Systems Inc
Prin QA Engineersan diego, CA30+ days ago
Required Qualifications Required education and experience: Associate''s Degree and 8-10 years'' experience OR Equivalent Combination of Relevant Education &/or Experience Critical professional related technical skills; computer skills: Proficient in Microsoft Office (Excel, Word, PowerPoint) Preferred Qualifications Preferred education and experience: Bachelor''s Degree Discipline/Major: Quality or Engineering degree preferred Knowledge, skills & abilities: Technical expertise. OTS empowers the U.S. military and its allies with an extensive range of overarching product segments applied across all levels of strategic and tactical operations, providing a cutting-edge advantage to our warfighters.
San Diego, CA30+ days ago
p>Job Description: About Us:
AMETEK Programmable Power Business Unit (~$160M) is headquartered in San Diego, CA and provides the most advanced Power and Instrumentation solutions for Precision Stimulus, Process Power and Measurement and Switching applications.
Champion activities to contribute and drive in the investigation and elimination of internal and external quality problems using applicable problem-solving techniques for determining Containment, Root Cause and Corrective/Preventive Action solutions along with Verification actions.
For specific work locations within San Jose, the San Francisco Bay area and New York City metropolitan area, the base pay range for this role is $79,500.00- $119,500.00/ annually. Learn more about Viasat's comprehensive benefit offerings that are focused on your holistic health and wellness at https://careers.viasat.com/benefits.
San Diego, CA30+ days ago
We are comprised of six, purpose-built centers of excellence throughout the USA and Mexico, each strategically focused on serving specific markets across aerospace engines and airframes, as well as munitions, radomes, antennas and fuel containment. Axillon Aerospace is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications.
Carlsbad, California22 days ago
If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information.. Summary: Under minimal supervision, the Quality Engineer I, will support Quality Management System activities that include document change control, data analysis and development of quality metric reports, support internal and external audits, conduct training, and manage training records, support internal and external corrective & preventive actions.
San Diego, CA30+ days ago
The position will be responsible to support change management activities, Nonconformances, equipment lifecycle, meeting facilitation and other ad hoc sustaining manufacturing requests. The position requires exceptional communication, interpersonal, and project management skills to effectively coordinate activities and deliver results.
This position involves designing and executing comprehensive test plans, building automated test suites, and collaborating closely with software developers, DevOps, and product teams to deliver robust, secure, and scalable solutions. Identify, document, and track defects using issue-tracking tools such as Jira; verify fixes and coordinate retesting cycles.
San Diego, CA30+ days ago
li>You have experience performing and reviewing software risk management activities, including Software Hazard Analysis (SHA), design FMEA, and change impact assessments for cloud, data, and AI/ML components.
You will drive pre‑market risk management deliverables, including Software Hazard Analysis (SHA), design FMEA, and risk controls related to cloud infrastructure, data processing, and AI/ML functionality.
Aliso Viejo, California25 days ago
The position focuses on identifying quality trends, improving product reliability, and ensuring timely resolution of quality issues through data-driven analysis and cross-functional collaboration. This role is responsible for supporting manufacturing and engineering quality activities, including defect analysis, root cause investigations, and customer return processes.
li style="white-space:pre-wrap;vertical-align:baseline;background-color:transparent;text-align:left">Generate and evaluate quality metrics to identify issues/trends and implement corrective/preventive actions to address nonconformances . Read and confirm compliance to Assembly Drawings, Bill of Materials (BOMs), Wire List, Engineering Drawings, Change Orders, and Rework Instructions .
The AI Quality Engineer leads quality assurance efforts for AI‑driven medical device software, overseeing end‑to‑end lifecycle development and compliance activities for Artificial intelligence (AI)/machine learning (ML) models to ensure safety, effectiveness, and regulatory alignment. The essential requirements of the job include: Bachelor's or master's degree in computer science, Data Science, Artificial Intelligence or a related technical field; advanced degree preferred, with 5+ years of quality experience in medical devices, IVD, or similarly regulated industries.
div> Job Summary:- Quality Engineer with experience in the Medical Device industry, specializing in quality engineering, design assurance, risk management, design controls, and product verification & validation. Roles & Responsibilities:
- Support quality engineering and design assurance activities within the Medical Device industry.