Quality engineer jobs in Pflugerville, TX

Job Tittle: Manufacturing Engineer-Sr Duration: 06 Months Contract As a member of the U.S. Orthopedics Operations Engineering team, you'll lead the planning and execution of manufacturing transfers across our global network. You'll coordinate technical readiness, validation activities, and process documentation to ensure smooth transitions between manufacturing sites. Key Responsibilities: • Execute end-to-end manufacturing and site transfer projects, including planning, risk assessment, validation, and handover. • Coordinate all technical documentation, process flows, and equipment readiness activities at both sending and receiving sites. • Support process and equipment validation (IQ/OQ/PQ) and ensure compliance with FDA and ISO 13485 requirements. • Partner cross-functionally with Quality, Regulatory, Supply Chain, Manufacturing, and R&D to ensure alignment and readiness. • Lead root cause analysis and technical problem-solving throughout the transfer lifecycle. • Prepare and maintain project documentation, including validation protocols, reports, and change control packages. • Communicate project progress, risks, and mitigation strategies to stakeholders at all levels. • Capture and share lessons learned to continuously improve future transfer processes. What You'll Need Success in this role requires technical expertise, attention to detail, and a collaborative mindset. You should be comfortable managing multiple priorities in a fast-paced, regulated environment. Required Qualifications: • Bachelor's degree in engineering, science, or related discipline. • Minimum of 4 years of experience in medical device manufacturing or other regulated industries. • Proven track record leading or supporting site or manufacturing transfers. • Or, proven track record of new product launches into existing sites. • Strong knowledge of process validation, change control, and manufacturing documentation. • Excellent problem-solving, communication, and organizational skills. • Ability to work independently and drive results with minimal supervision. Preferred Qualifications: • Experience with orthopedic implants, instruments, or precision assembly. • Familiarity with lean manufacturing and Six Sigma methodologies. • Proficiency with ERP, PLM, or MES systems.

Job Posting Start Date 11-21-2025 Job Posting End Date 02-27-2026Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a Quality Manager located in Austin, TX. Reporting to the Quality Director, the Quality Manager will be responsible to develop, implement, and coordinate product assurance program to prevent or eliminate defects in new or existing products. What a typical day looks like: Researches, evaluates and presents information concerning factors such as business situations, production capabilities, manufacturing problems, economic trends and design and development of new products for consideration by other members of management team. Suggests and debates alternative methods and procedures in solving problems and meeting changing market opportunities. Contributes with other top management personnel in formulating and establishing company policies, operating procedures and goals. Develops initial and subsequent modifications of product assurance program to delineate areas of control, personnel requirements and operational procedures within program. Evaluates contents of reports from product assurance program department heads and confers with top management personnel preparatory to formulating fiscal budget for product assurance program. Conducts management meetings with product assurance program department heads to establish, delineate and review program organizational policies, to coordinate functions and operations between departments, and to establish controls and procedures for attaining goals. Interface with customers on technical/quality issues and improvement initiatives. In charge of managing customer audits and regulatory/compliance agency audits. Reviews technical problems and procedures of departments and recommends solutions to problems or changes in procedures. Visits and confers with representatives of material and component vendors to obtain information related to supply quality, capacity of vendor to meet orders and vendor quality standards. Confers with engineers about quality assurance of new products designed and manufactured products on market to rectify problems. Reviews technical publications, articles, and abstracts to stay abreast of technical developments in industry.. The experience we're looking to add to our team: Bachelors degree in Engineering or Science. 10+ y of experience developing, implementing and maintaining quality systems in Medical Devices industry, including people management roles experience. Strong working knowledge of QMSR (Quality Management System) as well as ISO 13485 2016 (for medical devices) Quality tools (8's, 5 why, PFMEA, CAPA) Controls, Inspections in manufacturing process, incoming quality, laboratory Must have knowledge of national and international government regulatory agency standards. #LI-EA1 EA42 SS26 AA01 CH12 MS14 CC11 What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Job CategoryQuality Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

WHAT YOU DO AT AMD CHANGES EVERYTHING At AMD, our mission is to build great products that accelerate next-generation computing experiences-from AI and data centers, to PCs, gaming and embedded systems. Grounded in a culture of innovation and collaboration, we believe real progress comes from bold ideas, human ingenuity and a shared passion to create something extraordinary. When you join AMD, you'll discover the real differentiator is our culture. We push the limits of innovation to solve the world's most important challenges-striving for execution excellence, while being direct, humble, collaborative, and inclusive of diverse perspectives. Join us as we shape the future of AI and beyond. Together, we advance your career. THE ROLE: This dynamic, highly visible role drives product Quality & Reliability from concept to end of life to ensure a differentiated experience, improve customer satisfaction and build customer confidence. The suitable candidate will lead and be accountable for Quality & Reliability for all AMD datacenter CPU products. This is a high visibility role for highly experienced candidates. THE PERSON: Must have an excellent understanding of NPI flow to lead cross-functional activities across design, platform, operations, and customer system bring-up and manufacturing to meet product quality and reliability requirements. KEY RESPONSIBILITIES: * Influencing Fab and OSAT suppliers to meet product quality requirements including NUDD (New, Unique, Different, Difficult) for future technologies. * Define and manage product reliability qualification requirements and activities. * Measure and improve outgoing product quality through product end-of-life. * Maintaining robust Quality Processes & Quality Management Systems. * Close coordination with product/test engineering team for test gap debug and coverage solution implementation. * Interface between customer facing Customer Quality Engineering and the internal NPI team. PREFERRED EXPERIENCE: * Comfortable dealing with cross functional teams within AMD that requires structured problem solving and strong communication skills. * Experience in structured problem solving is necessary to ask questions in various "core team" meeting setting. * Extensive experience in product quality, reliability or product engineering, preferably in semiconductor industry. * Experience with semiconductor manufacturing and test flow fab, bump, assembly, test. * Highly organized, able to prioritize, and juggle multiple work streams to tight deadlines. * Ability to network, build relationships, and drive effective decision-making across multiple functions and levels within the organization is expected. ACADEMIC CREDENTIALS: * BS/MS/PhD in Electrical Engineering, Physics, Materials Science or similar. LOCATION: Austin, TX #LI-TW2 #LI-HYBRID Benefits offered are described: AMD benefits at a glance. AMD does not accept unsolicited resumes from headhunters, recruitment agencies, or fee-based recruitment services. AMD and its subsidiaries are equal opportunity, inclusive employers and will consider all applicants without regard to age, ancestry, color, marital status, medical condition, mental or physical disability, national origin, race, religion, political and/or third-party affiliation, sex, pregnancy, sexual orientation, gender identity, military or veteran status, or any other characteristic protected by law. We encourage applications from all qualified candidates and will accommodate applicants' needs under the respective laws throughout all stages of the recruitment and selection process.

In this role, you will be the Operations' technical owner responsible for end-to-end NPI manufacturing readiness starting from Proto build leading up to the OK2Ship milestone. You will partner closely with the Advanced Manufacturing Engineering (AME) teams including DFx, Test Engineering, Product Design Engineering, and with our manufacturing partners. You will be responsible to ensure overall manufacturing line readiness to enable NPI builds and its execution, and be also accountable to achieve manufacturing metrics and drive failure analysis and corrective actions (FACA). **Required Skills:** Product Quality Engineer Responsibilities: 1. Develop holistic manufacturing process flow, line layout, FA process flow, repair and rework process flow, headcount, and machine quantity during New Product Introduction (NPI) builds 2. Collaborate with cross-functional team to drive SMT and FATP Equipment & Fixture schedule and line readiness 3. Manage Major Issue List and facilitate technical discussion to resolve open issues, driving FACA to meet yield targets 4. Drive line cost savings through Capex & MVA reduction by utilizing yield bridge, UPH and OEE optimization 5. Drive development and implementation of repair and rework process flows 6. International travel to supplier sites, up to 25% **Minimum Qualifications:** Minimum Qualifications: 7. BS or higher in Business, Engineering, Supply Chain/Operations discipline or equivalent experience 8. Proven program/project management experience from NPI to high-volume MP 9. Experience working with international contract manufacturers 10. Background in process development, bring-up, and qualification, including Final Assembly, Test, Packout, and SMT processes 11. Knowledge of Design of Experiments and analytical problem-solving approaches 12. Cross-functional collaboration skills 13. Concise and clear communication **Preferred Qualifications:** Preferred Qualifications: 14. Demonstrated expertise in identifying, analyzing, and resolving complex technical issues within the hyperscaler manufacturing environment **Public Compensation:** $139,000/year to $200,000/year + bonus + equity + benefits **Industry:** Internet **Equal Opportunity:** Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.

Job DescriptionSUMMARY A detail-oriented Laboratory Technician to manage and perform calibration, verification, and maintenance of measurement and test equipment used throughout our manufacturing operations. The ideal candidate will ensure all equipment remains within specified tolerances and complies with internal quality systems and external standards (e.g., ISO 9001, ISO/IEC 17025, or other applicable requirements). ESSENTIAL DUTIES AND RESPONSIBILITIES Perform calibration, verification, and functional checks on a variety of instruments and equipment (e.g., pressure, temperature, dimensional, electrical, torque, and flow devices) Maintain and update calibration records, certificates, and traceability documentation in accordance with internal quality procedures Identify and segregate equipment found out of tolerance Coordinate repairs or adjustments with internal teams or external vendors Develop and maintain calibration schedules to ensure on-time service for all equipment Support root cause analysis and corrective actions for measurement-related nonconformances Work with quality and engineering teams to define calibration requirements for new or modified equipment Ensure all calibration activities meet relevant standards (e.g., NIST traceability, ISO/IEC 17025, or customer-specific requirements) Assist in audit preparation and provide technical support during internal and external audits. Maintain a clean, organized calibration area and follow all safety protocols and environmental procedures EDUCATION AND EXPERIENCE Education: Associate's degree in Metrology, Engineering Technology, Physics, or related technical field (or equivalent experience) Experience: 5+ years performing calibrations or working in a metrology or testing environment Familiarity with measurement principles, uncertainty, and common standards for dimensional, electrical, or mechanical calibration Ability to interpret technical drawings, specifications, and equipment manuals Strong computer skills and experience with calibration management software (e.g., GAGEtrak, IndySoft, or similar) Excellent attention to detail, recordkeeping, and organizational skills Ability to work independently and manage multiple priorities in a manufacturing environment CERTIFICATES, LICENSES, REGISTRATIONS Individuals must be able to perform the duties of the job at a level as generally prescribed and learned by attaining the credentials below. ASQ Certified Calibration Technician (CCT) preferred ASQ Certified Quality Technician (CQT) preferred PHYSICAL DEMANDS Ability to lift and move equipment up to 50 pounds Work may involve standing for extended periods or using fine motor tools Typical work environment: laboratory and production floor MANAGEMENT DISCLAIMER TECO-Westinghouse's Management reserves the right to revise, change or modify the duties and responsibilities of this position at any time to meet business and organizational needs. This position description may not list all duties for this position. The incumbent in the position may be asked to perform other duties. This position description is not a contract for employment and either the incumbent or TECO-Westinghouse may terminate employment at any time, for any reason. Powered by JazzHR 2eMynjmPfm

We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world. Team Description: Join our innovative Equipment Quality Team, a dynamic collective of experts dedicated to maintaining the precision and efficacy of high-tech equipment in preclinical and manufacturing domains. Engage with the latest in biomedical devices, industrial instrumentation, and high-end technologies like lasers and RF systems. As pioneers who've crafted a robust equipment program from scratch, we champion creative problem-solving and strive to set industry benchmarks. Immerse yourself in a mission-critical role that propels safety and regulatory compliance to new heights, and become part of a collaborative force driving the future of biomedical quality. Job Description and Responsibilities: Neuralink is seeking an Equipment Quality Technician with a strong knowledge of applied metrolog. This technician will calibrate, repair, and perform preventative maintenance on equipment in the quality program. In addition, they will troubleshoot and repair instruments and systems. This role requires participation in cross-functional teams and some travel. Additionally, you will be expected to: Calibrate and perform preventive maintenance on any instrument or device in the equipment quality program with little to no supervision Provide the technical expertise for assisting management in developing work procedures and protocols Assist in the design, fabrication, check-out, start-up, and acceptance of new or modified equipment Determine and requisition parts required for maintenance repairs Adhere to cGxP guidelines, SOPs, and safety rules/regulations Assist management with determining work schedules and project costs Work closely with cross-functional team members in regards to continuous improvement activities, solving problems, and improving overall product quality Explain calibration issues and processes to customers and management when needed Required Qualifications: Ability to comprehend and apply manuals and schematics for maintenance and troubleshooting Proficiency in using hand tools, physical/dimensional test instruments, and electronic test instruments Able to work in a dynamic, fast-paced environment Strong interpersonal skills: ability to work with colleagues and cross-functional teams in a professional and organized manner Competence in operating computing hardware and standard software Minimum of 1 year of experience related industrial instrumentation/calibration experience and/or training, or equivalent combination of education and experience Willingness to assist with other Quality Engineering activities such as facilities, equipment, and facilities validation Preferred Qualifications: Experience in PMEL, TMDE, Metrology, Calibration, Instrumentation, Validation, or Biomedical Equipment Associates or Bachelors Degree in Science, Technology, Engineering, Mathematics or military training in calibration Relevant experience working in a highly regulated (e.g., GMP, GCP, GLP) environments Expected Compensation: At Neuralink, your base pay is one part of your total compensation package. The anticipated hourly rate for this position is expected to be within the below range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. Texas Hourly Range: $20 - $34/Hr USD What We Offer: Full-time employees are eligible for the following benefits listed below. An opportunity to change the world and work with some of the smartest and most talented experts from different fields Growth potential; we rapidly advance team members who have an outsized impact Excellent medical, dental, and vision insurance through a PPO plan Paid holidays Commuter benefits Meals provided Equity (RSUs) *Temporary Employees & Interns excluded 401(k) plan *Interns initially excluded until they work 1,000 hours Parental leave *Temporary Employees & Interns excluded Flexible time off *Temporary Employees & Interns excluded

At Niagara, we're looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water. Consider applying here, if you want to: Work in an entrepreneurial and dynamic environment with a chance to make an impact. Develop lasting relationships with great people. Have the opportunity to build a satisfying career. We offer competitive compensation and benefits packages for our Team Members. Plant Quality TechnicianResponsible for executing corporate and plant specific Food Safety, Quality and Laboratory requirements. The QA Technician reports to QA Manager. In the absence of the Quality Assurance Technician, the QA Manager or designate will assume the job duties. Essential Functions Ensure all parameters of food safety and quality are being adhered to and maintained throughout the facility. Assist with batching chemicals/ingredients for production. Calibrate lab and line equipment for accurate results. Collect in-process and finished product samples. Conduct standardized qualitative and quantitative testing to ensure it meets specifications. Perform aseptic testing for microbial contamination. Follow protocols for documenting testing results. Recognize deficiencies and initiate proper follow-up. Identify and isolate product that does not meet standards. Aid in troubleshooting deficiencies and non-conformances. Review food safety and quality records. Actively participate in plant teams (HACCP, Safety, etc.) Conduct other duties as assigned by management. Please note this job description is not designed to contain a comprehensive list of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without prior notice. Qualifications Minimum Qualifications: 0 Years - Experience in Field or similar manufacturing environment 0 Years - Experience in Position 0 Years - Experience managing people/projects *experience may include a combination of work experience and education Must read, write and communicate in English. Must be able to work 12 hour shift (days or nights) on a rotating schedule Must follow GMP Policy - wear company issued shirt, hat, safety glasses, earplugs and hairnet in production areas. Able to lift up to 50 lbs. Able to work under pressure in a very fast paced environment Preferred Qualifications: 2 Years- Experience in Field or similar manufacturing environment 2 Years - Experience working in Position 2 Years - Experience managing people/projects *experience may include a combination of work experience and education Competencies This position embodies the values of Niagara's LIFE competency model, focusing on the following key drivers of success: Lead Like an Owner Makes safety the number one priority Keeps alert for safety issues and escalates immediately Effectively prioritizes tasks based on department goals Shows respect to others and confronts interpersonal issues directly Prioritizes resolution of customer issues effectively Responds promptly and honors commitments to internal and external customers InnovACT Makes recommendations to continuously improve policies, methods, procedures, and/or products Demonstrates adaptability by reacting appropriately to unexpected changes in situations or circumstances Increases performance through greater efficiency Find a Way Seeks to develop technical knowledge through learning from other experts Understands interdepartmental impact of individual decisions and actions Seeks solutions rather than placing blame Empowered to be Great Consistently looks for ways to improve one's self through growth and development opportunities Communicates clearly and promptly up, down, and across Communicates effectively to manage expectations Education Minimum Required: High School Diploma Preferred: Associate's Degree Certification/License: Required: N/A Preferred: HACCP Foreign Language Required: Full Professional Proficiency Preferred: None Required Benefits Our Total Rewards package is thoughtfully designed to support both you and your family: Regular full-time team members are offered a comprehensive benefits package, while part-time, intern, and seasonal team members are offered a limited benefits package. Paid Time Off for holidays, sick time, and vacation time Paid parental and caregiver leaves Medical, including virtual care options Dental Vision 401(k) with company match Health Savings Account with company match Flexible Spending Accounts Expanded mental wellbeing benefits including free counseling sessions for all team members and household family members Family Building Benefits including enhanced fertility benefits for IVF and fertility preservation plus adoption, surrogacy, and Doula reimbursements Income protection including Life and AD&D, short and long-term disability, critical illness and an accident plan Special discount programs including pet plans, pre-paid legal services, identity theft, car rental, airport parking, etc. Tuition reimbursement, college savings plan and scholarship opportunities And more! *********************************************** * *Los Angeles County applicants only** Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers, the California Fair Chance Act, and any other applicable local and state laws. Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity. Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees.

Job Description About Us Senseye is a NeuroTechnology Company in Austin, TX on the cusp of revolutionizing Mental Health. Over the past 6 years we have invested millions of dollars in R&D to build our platform allowing us to measure cognitive activity via the eye through mobile phones. Through multiple iterations and use cases we are now focused on building the world's first Objective Mental Health Diagnostics on top of our core technology. Our first diagnostic is for PTSD and is entering clinical trials now, followed soon by additional indications for Anxiety and Depression. As the world struggles with a mental health crisis, it is not hyperbolic to suggest that an objective diagnostic platform, that gives clinicians a safe and objective accurate approach to identifying and monitoring mental health disease, will redefine how mental health services are provided and will enable access to treatment for hundreds of millions of sufferers. The Senseye platform has the potential to be the technology that drives this change. Role Description We are seeking a Product Quality Engineer with strong experience in software and medical device quality systems to join our team. This individual will play a critical role in ensuring that our SaMD products meet regulatory, quality, and customer requirements throughout the product lifecycle-from development through post-market surveillance. Responsibilities Partner with Engineering, R&D, Regulatory, and Clinical teams to ensure compliance with ISO 13485, 21 CFR Part 820, IEC 62304, and other applicable standards. Support design and development activities by developing and reviewing documentation, ensuring design control compliance, and participating in design reviews. Perform risk management activities per ISO 14971, including creation and maintenance of risk analyses. Collaborate with development teams on cybersecurity requirements, threat modeling, vulnerability assessments, and post-market monitoring in accordance with FDA, ISO/IEC 27001, and other international standards to ensure product security. Define and implement non-product software validation strategies in alignment with FDA's CSA guidance, 21 CFR Part 11 and GAMP 5 principles. Contribute to the development and continuous improvement of the QMS, with a focus on software-specific quality processes. Investigate and resolve product quality issues, nonconformances, and CAPAs using root cause analysis techniques. Lead or support internal and external audits (e.g., FDA, Notified Bodies, ISO registrars). Participate in supplier qualification and software supplier evaluation processes. Monitor post-market product performance and contribute to complaint handling and field actions when needed. Drive quality metrics reporting and trend analysis to support management reviews and continuous improvement initiatives. Position requires access to Covered Defense Information for which the US Government requires US Citizenship You'll also need to pass an FBI background check Senseye maintains a drug free workplace and conducts pre-employment substance abuse testing. Senseye may also conduct substance abuse testing during employment, in accordance with its policies and customer requirements. Employment is subject to successfully completing and passing such tests. Requirements Bachelor's degree in Engineering, Computer Science, Life Sciences, or related technical discipline. 4+ years of experience in medical device quality engineering with 2+years in the SaMD environment (SaMD experience is a must!) Strong understanding of quality systems and regulatory frameworks, including ISO 13485, ISO 14971, IEC 62304, and 21 CFR Part 820/11. Experience with design control, risk management, and software validation. Familiarity with Jira, Confluence, and modern QMS or eQMS tools. Excellent communication, collaboration, and problem-solving skills. Extra Points: Perform agile software development/quality practices Perform Usability and Human Factor Engineering activities for medical devices Establish information security against HIPAA, GDPR requirements The compensation for this role is $97,000 - $121,000 annually. Benefits The freedom and trust to define your role as we design, build, and ship our products Competitive salary and stock option plan Flexible paid time off (vacation, sick leave, and public holidays) Flexible schedules Company health care plan Medical, dental, and vision insurance Short and long term disability insurance Life insurance policy 401k Commuter benefits for parking, public transit, carshares, etc. Mothers' room Fully stocked kitchen Opportunities for continuing education Senseye is dedicated to building a community of employees that are diverse, passionate, and engaged. We are committed to equal opportunity regardless of race, color, ancestry, religion, gender, gender identity, parental or pregnancy status, national origin, sexual orientation, age, marital status, disability, or veteran status. When we're safe, healthy, and balanced we can accomplish phenomenal things together.

At YETI, we believe that time spent outdoors matters more than ever and our gear can make that time extraordinary. When you work here, you'll have the opportunity to create exceptional, meaningful work and problem solve with innovative team members by your side. Together, you'll help our customers get the high-quality gear they need to make the most of their adventures. We are BUILT FOR THE WILD™. The Advanced Product Quality Engineer has primary responsibility of a product from “end to end lifecycle” from concept through the entire product development process, including once the product goes into the Wild. This includes product concept/requirement, design, validation, and manufacturing capability. Additionally, the APQE may take on supplier quality responsibilities directly or partner with global Supplier Quality Engineers (SQEs) to manage supplier quality for a portion of YETI's manufacturing partners and will be capable of delivering results in a fast paced and demanding environment. This person will have a significant level of partnership and engagement with project management, marketing, product development, manufacturing, and suppliers. He/She will work as a core team member on major product development projects. In addition, the advanced product quality engineer will be responsible for developing and standardizing processes and tools to better facilitate product development and manufacturing activities. More specifically, this individual's activities will be focused on bridging the design to the manufacturing and ensuring predictable quality through the product lifecycle. This is achieved through managing supplier qualification, ensuring solid manufacturing capability and driving PPAP on new/revised products, and thus serve as a bridge between new product development and manufacturing process approval and will be responsible to ensure that YETI's manufacturing partners are capable of producing high quality goods on an ongoing basis. Additionally, this role will be responsible to facilitate problem solving and sustaining activities on existing products, audit supplier processes for quality and conformance and drive continuous improvement activities related to product and process improvement. This role will also gather pre-shipment and ongoing warranty/reliability data, leverage LEAN tools and partnering with tier 1 and select tier 2 suppliers to drive continuous improvement, ultimately serving as the primary contact to funnel requested changes into the YETI system, and establish appropriate PPAP plans for product & process changes. Responsibilities: · Drive supplier quality throughout YETI's suppliers by partnering to implement manufacturing processes capable of ensuring a high degree of product conformance through the implementation of sustainable processes and statistical process controls · Work with cross functional teams and incorporate Advanced Product Quality Planning (APQP) in major product development projects and product changes; focus on Product requirement, Print reviews, DFx, FMEA, DVP, CAPA, Product and Process capability, Measurement System Analysis, Control Plans, and risk analysis · Drive the completion of Production Part Approval Process documentation packages with core team members and the suppliers · Analyze statistical data and product specifications to determine requirements and establish quality and reliability objectives · Work with suppliers to standardize processes, utilize metrics, and tools to improve product quality · Partner with YETI's suppliers to funnel required or requested changes through the change management process ultimately ensuring YETI's partners implement processes that drive a high degree of conformance and quality · Gather pre-shipment and warranty data related to specific YETI product families, leverage LEAN tools to establish root cause solutions and drive continuous improvement · Analyze new supplier capability as part of the supplier selection process · Drive continuous improvement by creating, maintaining, and implementing quality documentation such as SOPs, SIPs, workflows, standards libraries, manuals, etc. · Being the champion of customers and translate voice of customers into product requirement and design. Develop and maintain quality/reliability standards to ensure alignment with customer expectations · Perform quality reviews and internal audits on existing product development projects · Participate in supplier qualification and support sourcing decisions · Enthusiastically collaborate and drive a culture of quality, reliability, and continuous improvement throughout the organization Qualifications and attributes: · Bachelor's Degree in Engineering or related field is required · Greater than 5 years of engineering experience o (Hard Goods Space: with experience working with large tonnage, molded in color plastic injection parts, and processes) · Previous experience in quality and design engineering is preferred · Knowledge of quality tools, APQP, DFx, FMEA, DOE, GR&R, SPC, CAPA and PPAP · Knowledge of statistical methods and statistical analysis tools · Knowledge of reliability prediction methodologies · Ability to solve problems, perform risk analysis, make quality and timely decisions · Ability to lead and influence cross functional teams and being a team player · Ability to travel both internationally and domestically · Ability to solve problems, perform risk analysis, make quality and timely decisions. · Ability to lead and influence cross functional teams and being a team player. · Previous experience within a global full-service supply chain model. Additional Attributes - nice to have Knowledge and experience with a broad array of manufacturing methods, materials and tooling. Good vision and measured color perception. Additional computer skills preferred: PLM, SharePoint, Salesforce, Tableau, SolidWorks or other CAD software. Benefits & Perks: Click here to learn about the benefits and perks we offer at YETI. YETI is proud to be an Equal Opportunity Employer. Our commitment to creating a diverse, equitable, and inclusive culture is at the center of everything we do for our employees. We embrace all applicants looking to bring their authentic selves to YETI and contribute to our mission of keeping the wild WILD. Find out more about our commitment to DE&I at yeti.com/esg.html. All applicants for employment will be considered without regard to an individual's race, color, sex, gender identity, gender expression, religion, age, national origin or ancestry, citizenship, physical or mental disability, medical condition, family care status, marital status, sexual orientation, genetic information, military or veteran status, or any other basis protected by federal, state or local laws. YETI Applicant Privacy Notice YETI welcomes and encourages applications from people with disabilities. Accommodations are available upon request for candidates taking part in all aspects of the selection process. If you require accommodation in order to apply for a job, please contact us at accommodationrequest@yeti.com.

Kennedy Jenks is seeking a Drinking Water Process Engineer to provide technical expertise and support for drinking water treatment projects. The ideal candidate will have experience in drinking water treatment technologies and regulations, with a strong interest in continuing to develop their skills in water treatment. This role offers opportunities to work alongside experienced engineers and support clients on a variety of water quality and treatment projects. Key Responsibilities: Provide technical support for drinking water treatment projects, including treatment process evaluation, process selection, and operations optimization. Assist in preliminary engineering studies and feasibility assessments for municipal drinking water treatment systems. Support project teams with design and technical contributions, including developing process flow diagrams and design criteria for water treatment facilities. Collaborate with client service managers by contributing technical insights during project meetings and presentations. Participate in research and process improvements related to water quality and treatment technologies. Provide input on water treatment facility performance evaluations and assist in operations optimization. Stay engaged in water-focused professional organizations and present technical material at conferences. Qualifications: Bachelor's or Master's degree in civil / environmental engineering, or related scientific discipline required. 7+ years of experience in drinking water treatment engineering Practical professional engineer (PE) license or ability to obtain licensure within one year of hire. License in one or multiple states (CA, CO, FL, HI, OR, TX, VA, WA) preferred. Strong familiarity with drinking water treatment regulations and technologies. Ability to work as part of a project team, supporting senior staff and contributing to technical deliverables. Strong communication skills and ability to convey technical information clearly to colleagues and clients. Kennedy Jenks supports a healthy work-life balance and utilizes a hybrid model of home and office work, with a minimum of two days per week in the office. This approach empowers our people to thrive, collaborate, and achieve their full potential. The salary range for this position is anticipated to be $110,000 to $140,000, and may vary based upon education, experience, qualifications, licensure/certifications and geographic location. This position is eligible for performance and incentive compensation. #LI-Hybrid

Job DescriptionAbout Base Base is America's next-generation power company. We're rebuilding the foundation of modern civilization-electricity-by deploying a vast network of distributed batteries that is transforming today's fragile, centralized grid into a resilient and abundant system. We are engineers, operators, and creatives solving some of the most complex, interdisciplinary challenges of our time. About the Role We are looking for a manufacturing quality technician to join our team. This role focuses on continuous monitoring of the quality of our parts and processes throughout our manufacturing lines. You will conduct product-level testing and measurement, work with manufacturing and supplier engineering teams to identify and root cause manufacturing problems, validate new parts and processes, and manage non-conforming material. What You'll Do Perform measurements and testing of incoming material as part of our incoming quality control process Execute our manufacturing quality control plan by regularly testing parts and auditing processes and equipment Identify and manage non-conforming material throughout the manufacturing process, including quarantining of material, repair, and disposition Identify and investigate process abnormalities and excursions, working with process and equipment engineering teams to root cause issues and implement corrective actions Conduct process trials and design of experiments (DoEs) with cross-functional engineering teams to validate process and part improvements What You'll Bring 2+ years of experience working in a manufacturing or test lab environment or equivalent educational background in Mechanical/electrical engineering or similar. Ability to understand and interpret mechanical and electrical drawings and schematics. Working knowledge of geometric dimensioning and tolerancing (GD&T) and the ability to measure part features accordingly. Experience with CMMs, pCMMs or other high-precision dimensional metrology equipment and associated metrology software (PC-DMIS, Polyworks, etc.) strongly preferred Experience with various dimensional, mechanical, and electrical test and measurement tools (calipers, micrometers, force gauges, digital multimeters, etc.) Ability to work with and interpret data to drive action utilizing basic statistical analysis Who We Are Base is a company for people who want to win and who want their work to matter. We think from first principles, move with urgency, and treat the mission like our own. We talk about what isn't working before we talk about what is because every problem is an opportunity to fix something, improve the system, and compound progress. We cut through complexity, stay close to the work, and let results speak for themselves. Our Values First Principles Thinking: Question assumptions. Principles > rules. Operate at Base Pace: Focus on what matters, act quickly, and learn by doing. Give & Get Feedback: Be direct, be humble, and maintain a growth mindset. Everyone's an Owner: Follow through on commitments and own results. Strong Opinions, Loosely Held: Drive clarity and make calls with imperfect information. Committed to the Mission: Rebuilding the grid is a big challenge. We work hard because we care deeply about the impact we're creating. We work in-person. It's not a 9-to-5. We are all-in. Fun & Optimism Coexist with Grit: Collaboration and celebration coincide with the intensity of building real things. Do the best work of your life at Base.

Reports To: Quality & Warranty Manager Employment Type: Full-Time The Quality Technician is responsible for ensuring that all plumbing installations across active job sites meet internal quality standards, adhere to project specifications, and comply with safety and regulatory requirements. This role involves conducting inspections, generating detailed documentation, providing field-level support, and mentoring crew members on best practices. The ideal candidate is a proactive, detail-oriented professional with hands-on plumbing experience and has a strong commitment to quality and safety. Key Responsibilities: Jobsite Inspections Conduct routine and random inspections at active construction sites. Evaluate plumbing installations to ensure alignment with project plans, company standards, and local codes. Identify, document, and report deficiencies, hazards, or deviations from plans. Safety Oversight Monitor jobsite compliance with company safety standards and OSHA regulations. Proactively address and report unsafe conditions or practices. Field Support and Minor Repairs Perform minor plumbing repairs or adjustments in the field when necessary. Assist field crews with technical troubleshooting and guidance. Ensure the proper use of tools, materials, and PPE (personal protective equipment). Documentation and Reporting Maintain detailed inspection logs, quality assurance reports, and corrective action follow-ups. Learn and utilize digital reporting platforms for documentation and communication. Communicate findings with supervisors, project managers, and site leads. Training and Mentorship Assist in onboarding and training new field staff on quality control standards and safety protocols. Promote a culture of accountability, professionalism, and continuous improvement. Educate teams on new products or procedures. Qualifications: Minimum 3-5 years of experience in plumbing (residential or commercial). Current Journeyman Plumbing License required. Solid understanding of plumbing codes, materials, and modern installation practices. Strong knowledge of and adherence to OSHA safety standards. Ability to read and interpret blueprints and technical schematics. Strong verbal and written communication skills. Valid driver's license (with acceptable MVR) and reliable transportation required. Spanish-speaking skills preferred. Physical Requirements: Ability to walk, stand, kneel, stoop, and climb ladders for extended periods. Comfortable working in outdoor environments and active construction sites. Able to lift and carry loads up to 50 lbs.

Job Description Quality Technician-2nd shift is 2nd shift only (2p-10:30p) This position is responsible for monitoring parts and process quality and implementing and sustaining corrective and preventative actions and countermeasures. To perform this job successfully, an individual must be able to complete all areas outlined for this position in a satisfactory manner. The requirements listed below are representative of the knowledge, skills, and/or abilities to meet the minimum job requirements of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Essential Duties and Responsibilities Monitor part and process quality and implement and sustain corrective and preventative actions and countermeasures. Work closely with Process Engineering and Production team members to establish and sustain robust processes and procedures, which ensure consistent high quality. Audit manufacturing lines against approved manufacturing processes, procedures and requirements Verify and audit incoming, in-process and outgoing material to CelLink and Customer Quality and Engineering requirements and specifications. Promptly communicate emerging and trending quality issues. Lead and co-ordinate containment, sorting and MRB activities as needed. Support and participate in Quality System Development activities, New Product Launches, and Continuous Improvement Train operators/inspectors regarding quality, inspection and repair. Live the company culture of integrity, teamwork, self-discipline and professional competence Other duties as assigned Minimum Qualifications (Knowledge, Skills, and Abilities): To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below represent the required knowledge, skill, and/or ability. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions. Experience/Education: Engineering degree (Mechanical, Electrical, Manufacturing, Industrial, or similar) preferred but not required. Exceptions are based on years of experience in a similar role. One or more years of experience in a manufacturing, quality, or process focused role in a high-volume manufacturing environment. Knowledge/Skills/Abilities: Command of the English language, both written and verbal required. Mechanical inspection experience using basic and precision measurement tools (calipers, micrometers, thread gauges, etc.). Familiarity with common workplace software (Microsoft Office) Independent problem solver who desires to learn new skills and technology. Strong organizational skills and detail-oriented mindset. Ability to adapt to changing requirements in a fast-paced start-up setting. Excellent interpersonal and communication skills, strong work ethic, and ability to work in a collaborative team environment. Plusses: Experience in ISO 9001, IATF 16949, APQP, PPAP, FMEA, etc. Knowledge of Lean Manufacturing practices, 5S Prior start-up experience Physical Demands and Work Environment The physical demands described here represent those that an employee must meet to perform the essential functions of this position successfully. Reasonable accommodation may be made to enable individuals with disabilities to perform the functions. Working Conditions/Hours: Hourly Non-Exempt Physical Demands - Office and Manufacturing Environment While performing the duties of this position, the employee is regularly required to speak through a microphone or listen for software cues or other indicators that may not be presented visually. The employee must frequently use hands or fingers to handle or feel objects, tools, or controls. The employee must stand, walk, sit, and use hands and arms to pull/push, reach, climb, or balance; and. Periods of stooping, kneeling, crouching, or crawling may be required. The employee must lift and/or move up to 25 pounds without assistance. Specific vision abilities required by this position include close vision, distance vision, color vision, peripheral vision, and the ability to adjust focus are frequently required. Reasonable accommodation may be made to enable individuals with disabilities to perform the functions. Work Environment - Includes both a typical office environment, with minimal exposure to excessive noise or adverse environmental issues, and a shop environment, with exposure to high noise levels from operating machines, physical hazards from moving equipment and machine parts, nuisance dust, and skin exposure to chemicals used to run/maintain machines. PPE- Where required, must wear Personal Protective Equipment, including but not limited to safety glasses, safety shoes, bump caps, gloves, hair nets, masks, & clean-room frocks while adhering to the prescribed safety procedures.

Join Reynolds Consumer Products…and Drive Your Career across a world of opportunities! We provide amazing job opportunities for growth with competitive salaries and benefits in an exciting, dynamic, fast-paced, and high-performance organization. Are looking to build a strong career? Then we have an opportunity for you! We currently have an opening for a Process Engineer located at our facility in Temple, TX. Responsibilities Your Role: The Process Engineer role supports the manufacturing process using engineering skills to assess, manage, implement, improve, or revise processes, with the goal of improving efficiency of operation, safety, and the consistency of product quality. The individual will be responsible for developing procedures that facilitate the adoption of standardized processes that support future expansion. In addition, the individual will monitor the effectiveness of processes and quantifies results and presents findings to management. The role requires preparation of detailed reports and analysis for use by management in measuring overall production efficiency. You will have the opportunity to Make Great Things Happen! Achieve operational objectives by contributing information and recommendations to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, and quality; resolving problems; completing time studies; identifying trends; and implementing change. Draft and design layout of equipment, materials, and workspace to illustrate maximum efficiency, using drafting tools. Confer with vendors, and management personnel regarding purchases, procedures, product specifications, manufacturing capabilities, and project status. Knowledge of principles and methods for curriculum and training design, teaching and instruction for individuals and groups, and the measurement of training effects. Assess, document, and monitor existing processes. Implement and evaluate changes to existing processes designed to enhance productivity, safety, or product quality. Develop new processes as required. Interact closely with new product development group to assist in implementation and scale up of new products on the production lines. Analyze current machinery conditions and work with internal and external resources to modify and improve operational effectiveness. Lead facility in Lean Manufacturing efforts and education. You will love it here if… You put safety first, always. You listen, learn, and evolve. You are passionate about collaboration, teamwork, and achieving shared goals. You treat all people with respect, operating ethically, and embrace inclusivity. You are committed to improving our impact on local communities. Qualifications We need you to have: B.S. degree in Mechanical, Electrical or Industrial Engineering. 3-5 years of applicable technical experience required. Knowledge of raw materials, production processes, quality control, costs, and other techniques for maximizing the effective manufacture and distribution of goods. Knowledge of process-related standards. 5S and Lean experience. Mechanical aptitude and excellent technical, analytical and problem-solving skills (Root Cause analysis techniques required). Working knowledge of MS Office, MS Project, CAD, and Solidworks. Icing on the cake: MBA or other advanced degree a plus. Extrusion or reclaim experience preferred If you answer yes to the following…we want to meet you! Intellectual Curiosity: Do you have an inquisitive nature? Problem Solving: Do you have a knack for tackling issues head-on? Entrepreneurship: Do you enjoy taking ownership of your work? Customer Centricity: Do you always act in the best interests of the customer, putting their needs first? Growth Mindset: Do you focus on progress rather than perfection? Continuous Improvement: Are you never satisfied with the status quo? Want to know more? Check out our website or connect with us on LinkedIn! Apply today to join a fast-growing innovative company! Not a good fit but know someone who is? Please refer them! Local candidates only, no relocation assistance available Join Reynolds Consumer Products and Drive Your Career across a world of opportunities! For applicants or employees who are disabled or require a reasonable accommodation for any part of the application or hiring process, you may request assistance by emailing us at ******************************. No recruiter calls or emails please. RCP affords equal employment opportunities to applicants without regard to race, color, religion, age, disability status, sex, marital status, protected veteran status, pregnancy, national origin, genetics, genetic information, parental status, or any other characteristic protected by federal, state or local law. RCP conforms to the spirit as well as to the letter of all applicable laws and regulations. Posted Salary Range USD $80,000.00 - USD $90,000.00 /A

Job Posting Start Date 12-02-2025 Job Posting End Date 02-02-2026Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary The “Process Engineer” will be based onsite in Austin, TX. In charge for process-engineering capabilities focused on cost, quality and delivery improvements in order to hold up a manufacturing organization. Responsibilities: Recognize the manufacturing process, technologies, techniques and the product. Define, implement and evaluate proposed designs and processes for manufacturability. Have the capability to singly or with other engineering stakeholders identify root causes of failures in the manufacturing process. High level participation in daily production activities and effective problem solving on daily issues. Prepare justification, purchase and implement capital equipment for production. Hold up and oversee new process equipment production. Hold up the raising and introduction of engineering change orders (ECOs). Establish robust, repeatable and reproducible process parameters. Develop, implement and take ownership of process control methodologies. Trouble shoot process related issues. Participate in activities pertaining to cycle time and process improvements. Evaluate and select various engineered materials. Implement statistical process research on new and existing products. Implement safety, productivity and give in improvements. Improve manufacturing techniques and through put. Provide continuous development of manufacturing techniques that will improve in-house capabilities and gives in. Develop and maintain process documentation. Review processing methods. Interface with production of all activities associated with new process implementation and transfer. Assist in the development of training and provide training to production personnel during new technology transfer. Provide equipment maintenance and repair hold up as required. Guide cost improvement/reduction programs. Here is some of what you'll need (required): Typically requires a Bachelor's degree in related field or equivalent experience and training. Requires 2+ years of experience in engineering in the high technology electronics industry or related area. Willingness to learn new skills and work as part of a team Previous experience with factory lay out and process flow. Experience with MES is highly preferred Comfortable with customer facing environment Excellent verbal and written communication JS21 What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Job CategoryProduction Engineering Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

We are seeking a Product Quality Engineer to join our product quality engineering team, focusing on CPU / GPU server platforms. In this role, you will be responsible for ensuring the quality and reliability of CPU / GPU server products from development through mass production. You will collaborate closely with cross-functional teams including hardware design, manufacturing, supply chain, and data center operations to deliver best-in-class server solutions. Minimum Qualifications * Bachelor's degree in Electrical Engineering, Mechanical Engineering, Computer Engineering, or related field * 3+ years of experience in hardware quality engineering, preferably with server or data center hardware * Understanding of GPU / CPU architectures, server systems, and hardware validation methodologies * Familiarity with manufacturing processes, supplier management, and testing * Problem-solving, communication, and cross-functional collaboration skills Preferred Qualifications * Experience with large-scale data center deployments or hyperscale server environments * Prior experience working with GPU vendors and ODMs Responsibilities * Drive product development activities for GPU server products throughout the product lifecycle (NPI to mass production) * Develop test plans, and quality control processes for server hardware * Analyze manufacturing and field data to identify trends, root causes, and corrective actions for quality issues * Collaborate with design, sourcing and supplier teams to resolve technical issues and improve product quality * Lead failure analysis investigations and drive continuous improvement initiatives * Define and track key quality metrics * Support supplier quality engineering and manage quality escalations with vendors About Meta Meta builds technologies that help people connect, find communities, and grow businesses. When Facebook launched in 2004, it changed the way people connect. Apps like Messenger, Instagram and WhatsApp further empowered billions around the world. Now, Meta is moving beyond 2D screens toward immersive experiences like augmented and virtual reality to help build the next evolution in social technology. People who choose to build their careers by building with us at Meta help shape a future that will take us beyond what digital connection makes possible today-beyond the constraints of screens, the limits of distance, and even the rules of physics. Equal Employment Opportunity Meta is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, reproductive health decisions, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetic information, political views or activity, or other applicable legally protected characteristics. You may view our Equal Employment Opportunity notice here. Meta is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, fill out the Accommodations request form.

About Us Senseye is a NeuroTechnology Company in Austin, TX on the cusp of revolutionizing Mental Health. Over the past 6 years we have invested millions of dollars in R&D to build our platform allowing us to measure cognitive activity via the eye through mobile phones. Through multiple iterations and use cases we are now focused on building the world's first Objective Mental Health Diagnostics on top of our core technology. Our first diagnostic is for PTSD and is entering clinical trials now, followed soon by additional indications for Anxiety and Depression. As the world struggles with a mental health crisis, it is not hyperbolic to suggest that an objective diagnostic platform, that gives clinicians a safe and objective accurate approach to identifying and monitoring mental health disease, will redefine how mental health services are provided and will enable access to treatment for hundreds of millions of sufferers. The Senseye platform has the potential to be the technology that drives this change. Role Description We are seeking a Product Quality Engineer with strong experience in software and medical device quality systems to join our team. This individual will play a critical role in ensuring that our SaMD products meet regulatory, quality, and customer requirements throughout the product lifecycle-from development through post-market surveillance. Responsibilities Partner with Engineering, R&D, Regulatory, and Clinical teams to ensure compliance with ISO 13485, 21 CFR Part 820, IEC 62304, and other applicable standards. Support design and development activities by developing and reviewing documentation, ensuring design control compliance, and participating in design reviews. Perform risk management activities per ISO 14971, including creation and maintenance of risk analyses. Collaborate with development teams on cybersecurity requirements, threat modeling, vulnerability assessments, and post-market monitoring in accordance with FDA, ISO/IEC 27001, and other international standards to ensure product security. Define and implement non-product software validation strategies in alignment with FDA's CSA guidance, 21 CFR Part 11 and GAMP 5 principles. Contribute to the development and continuous improvement of the QMS, with a focus on software-specific quality processes. Investigate and resolve product quality issues, nonconformances, and CAPAs using root cause analysis techniques. Lead or support internal and external audits (e.g., FDA, Notified Bodies, ISO registrars). Participate in supplier qualification and software supplier evaluation processes. Monitor post-market product performance and contribute to complaint handling and field actions when needed. Drive quality metrics reporting and trend analysis to support management reviews and continuous improvement initiatives. Position requires access to Covered Defense Information for which the US Government requires US Citizenship You'll also need to pass an FBI background check Senseye maintains a drug free workplace and conducts pre-employment substance abuse testing. Senseye may also conduct substance abuse testing during employment, in accordance with its policies and customer requirements. Employment is subject to successfully completing and passing such tests. Requirements Bachelor's degree in Engineering, Computer Science, Life Sciences, or related technical discipline. 4+ years of experience in medical device quality engineering with 2+years in the SaMD environment (SaMD experience is a must!) Strong understanding of quality systems and regulatory frameworks, including ISO 13485, ISO 14971, IEC 62304, and 21 CFR Part 820/11. Experience with design control, risk management, and software validation. Familiarity with Jira, Confluence, and modern QMS or eQMS tools. Excellent communication, collaboration, and problem-solving skills. Extra Points: Perform agile software development/quality practices Perform Usability and Human Factor Engineering activities for medical devices Establish information security against HIPAA, GDPR requirements The compensation for this role is $97,000 - $121,000 annually. Benefits The freedom and trust to define your role as we design, build, and ship our products Competitive salary and stock option plan Flexible paid time off (vacation, sick leave, and public holidays) Flexible schedules Company health care plan Medical, dental, and vision insurance Short and long term disability insurance Life insurance policy 401k Commuter benefits for parking, public transit, carshares, etc. Mothers' room Fully stocked kitchen Opportunities for continuing education Senseye is dedicated to building a community of employees that are diverse, passionate, and engaged. We are committed to equal opportunity regardless of race, color, ancestry, religion, gender, gender identity, parental or pregnancy status, national origin, sexual orientation, age, marital status, disability, or veteran status. When we're safe, healthy, and balanced we can accomplish phenomenal things together.

Job DescriptionQuality Technician Reports To: Quality & Warranty Manager Employment Type: Full-Time The Quality Technician is responsible for ensuring that all plumbing installations across active job sites meet internal quality standards, adhere to project specifications, and comply with safety and regulatory requirements. This role involves conducting inspections, generating detailed documentation, providing field-level support, and mentoring crew members on best practices. The ideal candidate is a proactive, detail-oriented professional with hands-on plumbing experience and has a strong commitment to quality and safety. Key Responsibilities: Jobsite Inspections Conduct routine and random inspections at active construction sites. Evaluate plumbing installations to ensure alignment with project plans, company standards, and local codes. Identify, document, and report deficiencies, hazards, or deviations from plans. Safety Oversight Monitor jobsite compliance with company safety standards and OSHA regulations. Proactively address and report unsafe conditions or practices. Field Support and Minor Repairs Perform minor plumbing repairs or adjustments in the field when necessary. Assist field crews with technical troubleshooting and guidance. Ensure the proper use of tools, materials, and PPE (personal protective equipment). Documentation and Reporting Maintain detailed inspection logs, quality assurance reports, and corrective action follow-ups. Learn and utilize digital reporting platforms for documentation and communication. Communicate findings with supervisors, project managers, and site leads. Training and Mentorship Assist in onboarding and training new field staff on quality control standards and safety protocols. Promote a culture of accountability, professionalism, and continuous improvement. Educate teams on new products or procedures. Qualifications: Minimum 3-5 years of experience in plumbing (residential or commercial). Current Journeyman Plumbing License required. Solid understanding of plumbing codes, materials, and modern installation practices. Strong knowledge of and adherence to OSHA safety standards. Ability to read and interpret blueprints and technical schematics. Strong verbal and written communication skills. Valid driver's license (with acceptable MVR) and reliable transportation required. Spanish-speaking skills preferred. Physical Requirements: Ability to walk, stand, kneel, stoop, and climb ladders for extended periods. Comfortable working in outdoor environments and active construction sites. Able to lift and carry loads up to 50 lbs. Powered by JazzHR Hbod2PFa7M

Quality Technician 2nd shift only (2p-10:30p) The Quality Technician plays a critical role in ensuring that CelLink's products meet defined standards of quality, reliability, and performance. This position is responsible for inspecting materials and products at various stages of production, executing test procedures, and identifying non-conforming parts or processes. Quality Technicians support the manufacturing team by monitoring process quality, completing documentation accurately, and escalating quality concerns in a timely manner. Essential Duties and Responsibilities Monitor part and process quality, implement and sustain corrective and preventive actions, and countermeasures. Work closely with Process Engineering and Production team members to establish and sustain robust processes and procedures, which ensure consistent high quality. Audit manufacturing lines against approved manufacturing processes, procedures, and requirements. Verify and audit incoming, in-process, and outgoing material to CelLink and Customer Quality and Engineering requirements and specifications. Promptly communicate emerging and trending quality issues. Lead and co-ordinate containment, sorting, and MRB activities as needed. Support and participate in Quality System Development activities, New Product Launches, and Continuous Improvement. Train operators/inspectors regarding quality, inspection, and repair. Live the company culture of integrity, teamwork, self-discipline, and professional competence. Other duties as assigned. Minimum Qualifications (Knowledge, Skills, and Abilities) Experience/Education Engineering degree (Mechanical, Electrical, Manufacturing, Industrial, or similar) preferred but not required. Exceptions are based on years of experience in a similar role. One or more years of experience in a manufacturing, quality, or process-focused role in a high-volume manufacturing environment. Knowledge/Skills/Abilities: Command of the English language, both written and verbal, required. Mechanical inspection experience using basic and precision measurement tools (calipers, micrometers, thread gauges, etc.). Familiarity with common workplace software (Microsoft Office). Independent problem solver who desires to learn new skills and technology. Strong organizational skills and a detail-oriented mindset. Ability to adapt to changing requirements in a fast-paced start-up setting. Excellent interpersonal and communication skills, strong work ethic, and ability to work in a collaborative team environment. Plusses Experience in ISO 9001, IATF 16949, APQP, PPAP, FMEA, etc. Knowledge of Lean Manufacturing practices, 5S Prior start-up experience Physical Demands and Work Environment The physical demands described here represent those that an employee must meet to perform the essential functions of this position successfully. Reasonable accommodation may be made to enable individuals with disabilities to perform the functions. Working Conditions/Hours: Hourly Non-Exempt Physical Demands - Office and Manufacturing Environment While performing the duties of this position, the employee is regularly required to speak through a microphone or listen for software cues or other indicators that may not be presented visually. The employee must frequently use hands or fingers to handle or feel objects, tools, or controls. The employee must stand, walk, sit, and use hands and arms to pull/push, reach, climb, or balance. Periods of stooping, kneeling, crouching, or crawling may be required. The employee must lift and/or move up to 25 pounds without assistance. Specific vision abilities required by this position include close vision, distance vision, color vision, peripheral vision, and the ability to adjust focus are frequently required. Reasonable accommodation may be made to enable individuals with disabilities to perform the functions. Work Environment - Includes both a typical office environment, with minimal exposure to excessive noise or adverse environmental issues, and a shop environment, with exposure to high noise levels from operating machines, physical hazards from moving equipment and machine parts, nuisance dust, and skin exposure to chemicals used to run/maintain machines. PPE- Where required, must wear Personal Protective Equipment, including but not limited to safety glasses, safety shoes, bump caps, gloves, hair nets, masks, & clean-room frocks while adhering to the prescribed safety procedures. We believe diversity and inclusion among our teammates are essential to our success. We celebrate diversity and are committed to creating an inclusive environment for all employees while building teams that represent a variety of backgrounds, perspectives, and skills. We are an equal opportunity employer. All employment is decided based on qualifications, merit, and business needs. CelLink participates in the E-Verify program in specific locations as required by law. CelLink was founded in 2012 and entered volume production in 2018. CelLink provides electrical systems to the world's leading EV manufacturers, traditional automotive OEMs, and tiered suppliers. The company has raised approximately $315M in funding through private investment and multiple grants from the US Department of Energy. CelLink's investors include 3M, Atreides, BMW, BorgWarner, Bosch, D1 Capital, Fidelity, Fontinalis Partners, Ford, Franklin Templeton, Lear, Park West, SK Telecom, Standard Investments, T. Rowe Price, Tinicum, and Whale Rock .