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quality assurance engineer

TP-LINK

<div><p>Headquartered in the United States, <b>TP-Link Systems Inc. </b>is a global provider of networking devices and smart home products, consistently ranked among the world&rsquo;s leading providers of Wi-Fi devices. Serving customers in over 170 countries, TP-Link develops innovative technologies that connect millions of users and devices worldwide.</p><p>
At TP-Link, we believe technology can make life smarter, simpler, and more connected. We are committed to delivering high-quality products and cloud services that power modern networking, security, and smart home experiences.</p><p><b>
About the Role</b></p><p>
TP-Link is seeking a <b>Senior Software Quality Assurance Engineer </b>to join our growing <b>Cloud Services Quality Engineering </b>team. In this role, you will lead quality initiatives for cloud platforms that support millions of connected devices and users worldwide.</p><p>
You will be responsible for defining test strategies, driving automation, identifying quality risks, and ensuring the reliable delivery of scalable cloud services across TP-Link&rsquo;s networking and smart home ecosystem. Working closely with software engineers, architects, product managers, and fellow quality engineers, you will help shape the quality culture and engineering practices of our cloud platform organization.</p><p>
This role is ideal for an experienced quality engineer who is passionate about cloud technologies, backend systems, automation, and delivering exceptional customer experiences at scale.</p><p><b>
Responsibilities</b></p><ul><li>
Own quality planning, test strategy, and test execution for cloud service projects and backend systems.</li><li>
Serve as the quality owner for assigned projects, ensuring comprehensive test coverage and release readiness.</li><li>
Design and develop test plans, test cases, and testing approaches based on business requirements, system architecture, and risk analysis.</li><li>
Analyze distributed systems and microservices architectures to identify quality risks and testing opportunities.</li><li>
Validate cloud services through functional, integration, regression, API, database, and end-to-end testing.</li><li>
Develop, maintain, and enhance automated test frameworks and test suites to improve test coverage and efficiency.</li><li>
Integrate automated testing into CI/CD pipelines to support rapid and reliable software delivery.</li><li>
Perform backend validation using APIs, databases, logs, and monitoring tools.</li><li>
Execute performance, scalability, reliability, and resiliency testing for cloud services.</li><li>
Collaborate with development teams to investigate issues, reproduce defects, and support root cause analysis.</li><li>
Participate in architecture reviews, design discussions, and requirement analysis to ensure quality considerations are incorporated early in the development lifecycle.</li><li>
Drive continuous improvements in testing methodologies, automation practices, and quality engineering processes.</li><li>
Mentor junior engineers and promote quality engineering best practices across the team.</li><li>
Evaluate and adopt modern testing technologies, including AI-assisted tools, to improve engineering productivity and software quality.</li></ul><br>
<b>
Requirements</b><p><b><br>
Required Qualifications</b></p><ul><li>
Bachelor&rsquo;s degree in Computer Science, Software Engineering, or a related technical field.</li><li>
7+ years of experience in software quality engineering, backend system testing, or cloud service testing, with proven ability to define test strategies and lead quality initiatives for complex cloud systems.</li><li>
Strong understanding of microservices architectures and large-scale distributed systems, with the ability to analyze service interactions, identify quality risks, and develop effective testing strategies for cloud-based platforms.</li><li>
Hands-on experience testing RESTful APIs and backend services.</li><li>
Experience with Docker, Kubernetes, or other containerized environments.</li><li>
Familiarity with backend technologies such as Kafka, MySQL, MongoDB, Redis, or similar platforms.</li><li>
Experience working with AWS or other major cloud platforms.</li><li>
Hands-on experience with performance, scalability, reliability, and resiliency testing.</li><li>
Proficiency in Python or Java, with experience designing, developing, and maintaining automated test frameworks and scalable test automation solutions.</li><li>
Strong analytical, troubleshooting, debugging, and root cause analysis skills.</li><li>
Excellent communication skills and ability to collaborate effectively across engineering, product, and operations teams.</li></ul><p><b>
Preferred Qualifications</b></p><ul><li>
Experience leading quality initiative for complex projects or modules.</li><li>
Experience with IoT cloud platform, networking products, or smart home services.</li><li>
Knowledge of networking fundamentals, cloud security concepts, and observability tools.</li><li>
Experience leveraging AI-powered tools such as GitHub Copilot or other AI-assisted testing solutions to improve testing efficiency and engineering productivity.</li><li>
Mandarin and English bilingual proficiency is a plus.</li></ul><p><b>
Why Join TP-Link</b></p><ul><li>
Work on cloud services supporting millions of connected devices and users worldwide.</li><li>
Influence the quality strategy for industry-leading networking and smart home products.</li><li>
Build scalable automation solutions using modern cloud-native technologies.</li><li>
Collaborate with talented engineering teams across global locations.</li><li>
Gain exposure to large-scale distributed systems, IoT platforms, and AI-assisted engineering practices.</li><li>
Play a key role in shaping the future of TP-Link&rsquo;s cloud ecosystem and customer experience.</li></ul><br>
<b>
Benefits</b><p><i><br>
Salary Range: $135,000 - $170,000</i></p><ul><li>
Fully paid medical, dental, and vision insurance (partial coverage for dependents)
</li><li>Contributions to 401k funds
</li><li>15 days accrued vacation
</li><li>11 paid holidays
</li><li>Bi-annual pay increases
</li><li>Health and wellness benefits, including free gym membership
</li><li>Quarterly team-building events
</li></ul><p>At TP-Link Systems Inc., we are continually searching for ambitious individuals who are passionate about their work. We believe that diversity fuels innovation, collaboration, and drives our entrepreneurial spirit. As a global company, we highly value diverse perspectives and are committed to cultivating an environment where all voices are heard, respected, and valued. We are dedicated to providing equal employment opportunities to all employees and applicants, and we prohibit discrimination and harassment of any kind based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Beyond compliance, we strive to create a supportive and growth-oriented workplace for everyone. If you share our passion and connection to this mission, we welcome you to apply and join us in building a vibrant and inclusive team at TP-Link Systems Inc.</p><p><i>
Please, no third-party agency inquiries, and we are unable to offer visa sponsorship at this time.</i></p></div>

Senior Software Quality Assurance Engineer - Cloud Services

Edwards Lifesciences

<div><p>Imagine how your ideas and expertise can change a patient&rsquo;s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You&rsquo;ll bring your passion for problem solving and partner with various teams to influence decision-making for a product&rsquo;s entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.
</p><p></p><p>The Senior Software Quality Engineer is a key member of the Software Quality organization, responsible for ensuring the cybersecurity of product software including Software as a Medical Device (SaMD), Software in a Medical Device (SiMD), software as an accessory to a medical device, and other Digital Health Technologies. This role is responsible for owning and advancing product cybersecurity processes established within our Quality Management System and ensure alignment with applicable regulatory standards and industry guidance. The position will work in close partnership with R&amp;D, Product Security, Quality and other cross-functional team members to integrate cybersecurity requirements throughout the product software development lifecycle and support effective postmarket cybersecurity management.
</p><p></p><p>We are seeking an ambitious, technically strong candidate with a solid foundation in quality and cybersecurity, excellent communication skills, and the ability to build trusted relationships across the organization. This role offers meaningful opportunities to grow within a dynamic and evolving Software Quality function.
</p><p></p><p><b>How you will make an impact </b>:
</p><p></p><ul><li>Own the establishment, implementation, and continuous improvement of cybersecurity related processes for product software established in our Quality Management System
</li><li>Review and approve product cybersecurity related deliverables across the lifecycle, including planning, requirements, architecture/design, risk management, verification and validation, and problem resolution (dispositioning of cybersecurity vulnerabilities and defects).
</li><li>Execute Cybersecurity risk analysis on our products.
</li><li>Provide assurance that all requirements related to cybersecurity are followed when developing or making changes to product software.
</li><li>Work in close partnership with Product Security, Quality and R&amp;D to address and monitor cybersecurity risks throughout the Product Software Development Lifecycle.
</li><li>Support regulatory submissions and responses regarding cybersecurity related requests.
</li><li>Effectively manage multiple priorities, projects and ability to communicate at all levels of personnel.
</li><li>Author, review and approve documents in our Application Lifecycle Management and Product Lifecycle Management systems.
</li><li>Willingness to work in a fast-paced, dynamic environment to meet the needs of the business and deliver safe quality products to our patients.
</li></ul><p></p><p><b>What you will need (Required):
</b></p><p></p><ul><li>Bachelor&rsquo;s degree in Scientific, Engineering, or Computer Science fields plus four (4) years of relevant work experience; OR Master&rsquo;s degree Scientific, Engineering, or Computer Science fields plus three (3) years of relevant work experience.
</li><li>Highly regulated industry experience
</li><li>Experience with software development and/or software quality in regulated environments
</li></ul><p></p><p><b>What else we look for (Preferred):
</b></p><p></p><ul><li>Engineering or Computer Science degree
</li><li>Medical device industry experience
</li><li>Experience with cybersecurity risk assessments
</li><li>Experience integrating cybersecurity into the SDLC / design controls
</li><li>Familiarity with vulnerability management and post market cybersecurity processes
</li><li>Familiarity with software (IEC 62304) and cybersecurity (NIST) guidelines; including understanding of Waterfall and Agile concepts in context with the SDLC process.
</li><li>Knowledge and experience in Medical Device Risk Management (ISO 14971)
</li><li>Excellent written and verbal communication skills required.
</li></ul><p></p><p>Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
<br>
<br>
For California (CA), the base pay range for this position is $108,000 to $153,000 in tool (highly experienced).
<br>
<br>
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
</p><p></p><p>E dwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
</p><p></p><p><b>COVID Vaccination Requirement
</b></p><p>Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.</p></div>

Senior Software Quality Engineer - Cybersecurity

Katalyst Healthcares & Life Sciences

<div><b>Job Description:</b><br>
We are seeking a highly experienced Principal Quality Engineer to lead quality engineering initiatives in a regulated manufacturing environment. This role provides technical leadership for quality systems, product quality improvements, risk management, CAPA activities, process validation, and compliance programs. The Principal Quality Engineer serves as a subject matter expert, partnering with cross-functional teams to ensure products meet customer, regulatory, and business requirements while driving continuous improvement and operational excellence.<br>
<b>Responsibilities:</b>
<ul><li>Provide technical leadership and mentorship to Quality Engineers and cross-functional teams.
</li><li>Lead complex investigations involving customer complaints, nonconformances, deviations, and product quality issues.
</li><li>Drive root cause analysis using methodologies such as 8D, Fishbone, 5 Whys, Fault Tree Analysis, and FMEA.
</li><li>Lead CAPA development, implementation, effectiveness verification, and closure activities.
</li><li>Ensure compliance with FDA regulations, ISO 13485, ISO 14971, GMP, and other applicable quality standards.
</li><li>Support product development activities including Design Controls, Risk Management, Verification &amp; Validation, and Design Transfer.
</li><li>Develop and maintain quality plans, inspection strategies, control plans, and quality metrics.
</li><li>Analyze quality trends and manufacturing data to identify opportunities for process improvement and risk reduction.
</li><li>Lead internal and external audits, supplier audits, and regulatory inspections.
</li><li>Collaborate with Manufacturing, R&amp;D, Operations, Regulatory Affairs, and Supply Chain teams to resolve quality issues.
</li><li>Review and approve validation protocols and reports including IQ, OQ, PQ, TMV, and process validations.
</li><li>Support supplier quality management activities including supplier qualification and performance monitoring.
</li><li>Drive continuous improvement projects utilizing Lean, Six Sigma, and statistical process control methodologies.
</li><li>Review engineering changes and assess quality and regulatory impacts.
</li><li>Present quality performance metrics and recommendations to senior management.
</li></ul><h3 class="jobSectionHeader"><b>Requirements:</b><b>
</b></h3><ul><li>Bachelor's degree in engineering, Quality, Biomedical Engineering, Mechanical Engineering, Manufacturing Engineering, or related technical field.
</li><li>8 15+ years of quality engineering experience in Medical Device, Pharmaceutical, Biotechnology, Aerospace, or highly regulated industries.
</li><li>Strong knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, GMP, and quality management systems.
</li><li>Extensive experience with CAPA, complaint handling, investigations, risk management, and process validation.
</li><li>Experience leading audits and interacting with regulatory agencies.
</li><li>Strong statistical analysis and problem-solving skills.
</li><li>Proficiency with quality tools including Minitab, SPC, DOE, FMEA, Control Plans, and Risk Assessments.
</li><li>Excellent technical writing, communication, and leadership skills.
</li></ul><h3 class="jobSectionHeader"><b>Preferred Qualifications:</b><b>
</b></h3><ul><li>Master's degree in engineering or related field.
</li><li>ASQ Certifications such as:
<ul><li>Certified Quality Engineer (CQE)
</li><li>Certified Six Sigma Black Belt (CSSBB)
</li><li>Certified Manager of Quality/Organizational Excellence (CMQ/OE)
</li></ul></li><li>Experience with medical device product lifecycle management.
</li><li>Experience supporting global manufacturing operations.
</li></ul><h3 class="jobSectionHeader"><b>Key Skills:</b><b>
</b></h3><ul><li>Quality Systems Management.
</li><li>CAPA Leadership.
</li><li>Root Cause Analysis.
</li><li>Design Controls.
</li><li>Risk Management (ISO 14971).
</li><li>Process Validation.
</li><li>Statistical Analysis.
</li><li>Supplier Quality.</li></ul></div>

Principal Quality Engineer

Medtronic

<div>We anticipate the application window for this opening will close on - 22 Jun 2026<br>
<p></p><br>
<p>At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You&rsquo;ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
</p><p></p><h1 class="jobSectionHeader"><b>A Day in the Life
</b></h1>At Medtronic, we act boldly, compete to win, move with speed, foster belonging, and deliver results&mdash;the right way. This is the Medtronic Mindset, defining how we work and what we value. Our brand is rooted in action, and every team member plays a vital role in bringing our culture to life.
<br>
<br>
We recognize your extraordinary potential to help ensure future generations live better, healthier lives. A career at Medtronic is purposeful, mission-driven, and unlike any other. We are committed to alleviating pain, restoring health, and extending life for millions worldwide. As a Supplier Quality Engineer based in Irvine, CA you will support the Neurovascular Operating Unit by ensuring externally sourced materials, components, and services consistently meet Medtronic quality and regulatory requirements. This role partners closely with Neurovascular R&amp;D, Manufacturing, Operations Quality, and Sourcing to qualify and develop suppliers, support new product introductions and design changes, and resolve supplier-related nonconformances that could impact product performance or patient safety. You will lead investigations and root cause analysis for supplier issues, drive corrective and preventive actions with suppliers, and monitor performance through robust metrics and reviews. By building strong technical relationships with key suppliers and championing continuous improvement, this role helps maintain reliable supply and high first-time quality for Neurovascular products manufactured in Irvine, CA.
<br>
<br>
Onsite: At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We&rsquo;re working a minimum of 5 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.<br>
<p></p><p><b>Responsibilities may include the following and other duties may be assigned:
</b></p><ul><li><p>Ensures that suppliers deliver quality parts, materials, and services.
</p></li><li><p>Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness.
</p></li><li><p>Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur.
</p></li><li><p>Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation.
</p></li><li><p>Some individuals may have responsibilities that include Pre-Market Supplier Quality and duties may include: Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products.
</p></li><li><p>Provides technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements.
</p></li><li><p>Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products.
</p></li><li><p>Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods.
</p></li><li><p>Lead qualification and onboarding of new suppliers, including quality assessments, audits, and documentation review.
</p></li><li><p>Support risk management activities related to supplied materials and processes.
</p></li><li><p>Partners with Site R&amp;D, Quality, and Manufacturing Engineering to assist in developing test methods, equipment acquisition for new product testing, validations/qualifications, statistical analysis of data for significance, and other documented requirements for quality objectives.
</p></li><li><p>Lead investigations for supplier-related nonconforming material and complaints; perform root cause analysis and implement sustainable corrective actions
</p></li></ul><p></p><p><b>Must Have: Minimum Requirements
</b></p><p><i>To be considered for this role, please ensure the minimum requirements are evident in your applicant profile </i><b><i>.
</i></b></p><ul><li><p>Requires a Baccalaureate degree and minimum of 4 years of relevant experience OR Master's degree with a minimum of 2 years relevant experience OR PhD with 0 years relevant experience
</p></li></ul><p></p><p><b>Nice to Have
</b></p><ul><li><p>Experience working with medical device or highly regulated industries (FDA, ISO 13485, MDR, etc.)
</p></li><li><p>ASQ certifications such as Certified Quality Engineer (CQE), Certified Supplier Quality Professional (CSQP), or Certified Six Sigma Black/Green Belt
</p></li><li><p>Experience with supplier development and supplier performance improvement programs
</p></li><li><p>Demonstrated success in leading supplier audits (process, quality system, or compliance audits)
</p></li><li><p>Familiarity with risk management methodologies such as ISO 14971 and FMEA
</p></li><li><p>Experience supporting new product development (NPD) or design transfer to suppliers
</p></li><li><p>Strong background in advanced quality tools (SPC, MSA, DOE, capability analysis)
</p></li><li><p>Experience implementing or improving supplier corrective action (SCAR/CAPA) systems
</p></li><li><p>Experience working with contract manufacturers and global supply chains
</p></li><li><p>Exposure to manufacturing process validation (IQ/OQ/PQ) at supplier sites
</p></li><li><p>Experience with APQP, PPAP, and control plan development
</p></li><li><p>Familiarity with digital quality systems such as TrackWise, MasterControl, SAP, or similar QMS platforms
</p></li><li><p>Experience with component or process qualification for complex technologies (electronics, polymers, machining, sterile processing, etc.)
</p></li><li><p>Ability to analyze supplier quality metrics and drive continuous improvement initiatives
</p></li><li><p>Experience influencing suppliers and cross-functional teams without direct authority
</p></li><li><p>International supplier engagement experience or willingness to travel for supplier support and audits.
</p></li></ul><p>For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. &sect; 214.2(h)(4)(iii)(A) is required.
</p><p></p><p><b>Physical Job Requirements
</b></p><p></p><p>The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
</p><p></p><p>The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
</p><p></p><p><b>U.S. Work Authorization &amp; Sponsorship
</b></p><p>At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
</p><p>Join us in our mission to alleviate pain, restore health, and extend life&mdash;where your unique background and perspective are valued.
</p><h1 class="jobSectionHeader"><b>Benefits &amp; Compensation<br>
</b><br>
</h1><p><b>Medtronic offers a competitive Salary and flexible Benefits Package
</b><br>
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.<br>
<br>
</p><p></p>Salary ranges for U.S (excl. PR) locations (USD):$99,200.00 - $148,800.00<br>
<p></p>This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
<p></p>The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
<p></p><p>The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance , Health Savings Account , Healthcare Flexible Spending Account , Life insurance, Long-term disability leave , Dependent daycare spending account , Tuition assistance/reimbursement , and Simple Steps (global well-being program).<br>
</p><p></p><p>The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match , Short-term disability , Paid time off , Paid holidays , Employee Stock Purchase Plan , Employee Assistance Program , Non-qualified Retirement Plan Supplement (subject to IRS earning minimums) , and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).<br>
</p><p></p><p>Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.<br>
</p><p></p><p>Further details are available at the link below:
</p><p>Medtronic benefits and compensation plans
</p><p></p><h1 class="jobSectionHeader"><b>About Medtronic
</b></h1><p>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
<br>
Our Mission &mdash; to alleviate pain, restore health, and extend life &mdash; unites a global team of 95,000+ passionate people.
<br>
We are engineers at heart&mdash; putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
</p><p></p><p>Learn more about our business, mission, and our commitment to diversity here .
</p><p></p><p>It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
</p><p></p><div><div><div><div><div><div><div><p>If you are applying to perform work for Medtronic, Inc. (&ldquo;Medtronic&rdquo;) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.</p></div></div></div></div></div></div></div></div>

Senior Supplier Quality Engineer

<div><p>Imagine how your ideas and expertise can change a patient&rsquo;s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You&rsquo;ll bring your passion for problem solving and partner with various teams to influence decision-making for a product&rsquo;s entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology. In this role, you will apply your knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution.
</p><p></p><div><b>How you will make an impact:
</b><br>
<ul><li>Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports.
</li><li>Optimize moderately complex Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk
</li><li>Develop, update, and maintain technical content of risk management files
</li><li>Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes
</li><li>Assign support tasks; gives instruction to technicians on conducting tests; trains technicians and provides feedback; and may coordinate technician work.
</li><li>Other incidental duties assigned by Leadership
</li></ul></div><p></p><div><b>What you'll need (Required):
</b><br>
<ul><li>Bachelor's Degree in Engineering or Scientific field, 2 years&rsquo; experience related work experience or
</li><li>Master's Degree or equivalent in and internship, senior projects or thesis in Engineering or Scientific field including either industry or industry/education
</li></ul></div><p></p><div><b>What else we look for (Preferred):
</b><br>
<ul><li>Good documentation, communication and interpersonal relationship skills including negotiating and relationship management skills
</li><li>Basic understanding of statistical techniques
</li><li>Previous experience working with lab/industrial equipment required
</li><li>Solid understanding and knowledge of principles, theories, and concepts relevant to Engineering
</li><li>Solid problem-solving, organizational, analytical and critical thinking skills
</li><li>Solid understanding of processes and equipment used in assigned work
</li><li>Knowledge of and adherence to Quality systems
</li><li>Strict attention to detail
</li><li>Ability to interact professionally with all organizational levels
</li><li>Ability to manage competing priorities in a fast paced environment
</li><li>Must be able to work in a team environment, including the ability to manage vendors and project stakeholders
</li><li>Ability to build productive internal/external working relationships
</li><li>Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health &amp; Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
</li></ul></div><p></p><p>Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families. For California, the base pay range for this position is $87,000 - $123,000 (highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
</p><p></p><p>E dwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
</p><p></p><p><b>COVID Vaccination Requirement
</b></p><p>Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.</p></div>

Pilot Quality Engineer II - Sheaths

Stellar Consulting Solutions, LLC

<div>
 <p>
  <strong>
   Role: Supplier Quality Analyst
  </strong>
 </p>
 <p>
  <strong>
   Location: Irvine, CA(Onsite)
  </strong>
 </p>
 <p>
  <strong>
   Duration: 6+Months(Contract#w2)
  </strong>
 </p>
 <p>
  <strong>
   Client: Medical
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Education Bachelor Engineering or Quality
 </p>
 <p>
  Windchill / PLM Will red line Doc's
 </p>
 <p>
  Doc control , Validating systems , Updating supplier change request , reveiwing Quality Agreements
 </p>
 <p>
  <strong>
   Job Summary
  </strong>
 </p>
 <p>
  The Supplier Quality Analyst is responsible for ensuring that suppliers of materials, components, and services used in medical devices consistently meet quality, regulatory, and risk requirements. This role supports compliance with FDA Quality System Regulation (21 CFR 820), ISO 13485 through supplier performance monitoring, corrective action management, and risk-based supplier controls.
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Manage and maintain supplier qualification, monitoring, and re-evaluation activities in accordance with 21 CFR 820.50 (Purchasing Controls) and ISO 13485.
  </li>
  <li>
   Monitor supplier quality performance using KPIs such as defect rates, corrective action trends, and supplier risk levels.
  </li>
  <li>
   Maintain approved supplier lists (ASL) and supplier quality records per document control requirements.
  </li>
  <li>
   Issue, track, and evaluate Supplier change requests.
  </li>
  <li>
   Escalate supplier quality risks and support remediation and improvement plans.
  </li>
  <li>
   Review and support supplier-initiated or internally driven changes that may impact product quality or compliance (materials, processes, manufacturing location).
  </li>
  <li>
   Collaborate with Engineering and Regulatory Affairs to assess supplier changes requiring validation, verification, or regulatory impact evaluation.
  </li>
  <li>
   Provide supplier quality input for management reviews and quality metrics.
  </li>
  <li>
   Ensure supplier quality documentation is accurate, complete, and maintained in the electronic Quality Management System (eQMS).
  </li>
  <li>
   Ensure supplier activities comply with internal procedures, regulatory requirements, and quality system expectations.
  </li>
 </ul>
 <p>
  <strong>
   Required Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Engineering, Quality, or a related field; or equivalent experience.
  </li>
  <li>
   2&ndash;5 years of experience in Supplier Quality, Quality Assurance, or Manufacturing within a medical device or other regulated environment.
  </li>
  <li>
   Working knowledge of 21 CFR 820, ISO 13485, and supplier control requirements.
  </li>
  <li>
   Proficiency in Microsoft Excel and data analysis.
  </li>
 </ul>
 <p>
  <strong>
   Key Skills &amp; Competencies
  </strong>
 </p>
 <ul>
  <li>
   Strong understanding of regulated quality systems
  </li>
  <li>
   Analytical, detail-oriented problem-solving mindset
  </li>
  <li>
   Clear written and verbal communication
  </li>
  <li>
   Ability to influence suppliers and internal stakeholders
  </li>
  <li>
   Strong organizational and time-management skills.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  kindly share resume at gaurav@stellarconsulting.com or call me at 678-935-7045 to discuss more!
 </p>
</div>


Supplier Quality Assurance

Tata Consultancy Services (TCS)

<div></div><div><div><div><div><div>BAU/L3 Support _ Data Engineer &ndash; L3 Support Engineer (Lead)</div><br>
<div></div><br>
<div>This role requires coordination between onshore, nearshore, and offshore teams</div>
<div>Required Skills</div>
<ul><li> Strong experience with Databricks, Apache Spark, and performance tuning.
</li></ul><ul><li> Expertise in Apache Airflow/Astronomer for workflow orchestration and DAG design.
</li></ul><ul><li> Deep understanding of Data Engineering, ETL/ELT, and large-scale data platforms.
</li></ul><ul><li> Experience with CI/CD, DevOps, Infrastructure as Code (IaC), and automation.
</li></ul><ul><li> Strong platform management, monitoring, and incident management experience.
</li></ul><ul><li> Excellent leadership and stakeholder management skills.
</li></ul><div>Preferred Domain Experience</div>
<ul><li> Asset Management
</li></ul><ul><li> Investment Management
</li></ul><ul><li> Capital Markets
</li></ul><ul><li> Portfolio &amp; Market Data Platforms<br>
</li></ul><div></div><br>
<div>Job Summary</div>
<div>We are seeking an experienced Data Engineering Tower /Pod Lead with a strong background in Asset Management to lead enterprise-scale data engineering initiatives. The ideal candidate will be responsible for end-to-end data delivery, platform stability, and managing multiple data engineering pods while ensuring alignment with business and investment management objectives.</div>
<div>Key Responsibilities</div>
<ul><li> Lead and manage the Data Engineering Tower, overseeing multiple teams and delivery pods.
</li></ul><ul><li> Own end-to-end data platform delivery, operational excellence, and SLA adherence.
</li></ul><ul><li> Drive scalable data pipeline development, data quality, and platform reliability.
</li></ul><ul><li> Manage cross-functional dependencies, stakeholder communication, and issue escalations.
</li></ul><ul><li> Ensure high availability, monitoring, alerting, and production support readiness.
</li></ul><ul><li> Collaborate with business, portfolio management, and technology leadership teams.
</li></ul><div>Define and implement best practices for platform governance, operational readiness, and performance optimization</div><br>
<div></div><br>
<div>Salary Range- $110,000-$150,000 a year</div>
</div></div></div><div><div><div>Location
</div><div>Irvine, CA
</div></div><div><div>Job Function
</div><div>TECHNOLOGY
</div></div><div><div>Role
</div><div>Lead
</div></div><div><div>Job Id
</div><div>417458
</div></div><div><div>Desired Skills
</div><div>Apache Spark
</div></div><div><div>Salary Range
</div><div>$110,000-$150,000 a year</div></div></div></div><div></div>

BAU_L3 Support_Data Engineer

Explore 36+ Quality assurance engineer in Irvine this July. Find roles across top companies and apply now to boost your career.