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supplier quality engineer

Hansae Mobility US Manufacturing

Job SummaryThe Supplier Quality Engineer (SQE) will be the technical liaison between HANSAE Mobility purchasing, product engineering, manufacturing, and our supply base. In this role, the Supplier Quality Engineer will work with the suppliers to resolve supplier manufacturing and quality issues, implement and monitor advanced quality planning systems, and provide technical support throughout the lifecycle of the assigned components.Duties and Responsibilities<ul><li>Assure supplier understanding and compliance with APQP processes and product PPAP submission and approval requirements.</li><li>Review and approve supplier quality plans (Control Plans, PFMEA, etc.) of new components and assemblies for new vehicles.</li><li>Review and audit supplier manufacturing processes and quality systems.</li><li>Support on internal improvement actions related to supplier quality issues.</li><li>Perform on-site or remote supplier root cause analysis and verification of corrective actions of supplier quality issues.</li><li>Implement and monitor supplier part qualification and certification processes (PPAP, Run and rate, etc.).</li><li>Improve quality performance of suppliers by conducting onsite workshops at supplier locations, providing technical assistance in developing a robust quality system, or other technical support as required.</li><li>Provide technical assistance during supplier launch, changeover and ongoing production activities.</li><li>Maintain a supplier performance database including metric scorecard reporting.</li><li>Manage incoming material inspection program including supervision of incoming material inspectors.</li><li>Update indicators of internal and external supplier quality performance on a regular basis.</li><li>Conduct internal product audits.</li><li>Support internal and external audits, including customers audits.</li><li>Manage non-conforming materials such as trace, hold, sort, certify, and containment activities in the event of an issue, as well as managing the Quality Cage.</li><li>Promote and support continuous improvement activities focused on defect reduction and process optimization (internal or at supplier).</li><li>Ensure ongoing compliance with the Quality Management System (QMS) and applicable standards (IATF 16949, ISO 9001, VDA 6.3).</li><li>Other duties as assigned.</li></ul>Education &amp; LanguageMinimum degree: <ul><li>Bachelor&rsquo;s degree in engineering (Mechanical, Industrial, Electrical, Manufacturing, or Materials preferred).</li><li>Other Technical and Quality Certifications are a plus</li></ul>Required skills and Experience<ul><li>Minimum five years of experience in quality, engineering and/or manufacturing.</li><li>Quality Systems Planning (APQP), including PPAP.</li><li>Control Plan &amp; FMEA (Failure Mode and Effects Analysis).&bull;</li><li>Proficient in print reading and interpretation, part measurement, gage design and function.</li><li>Experience working with an OEM or Tier 1 in automotive.</li><li>Knowledge of geometric design and tolerancing (GD&amp;T).</li><li>Knowledge of manufacturing and assembly plant processes, procedures, tooling, equipment and facilities layout.</li><li>Knowledge of Quality &amp; statistical tools (8Ds, 5 Whys, Fishbone, SPC, design of experiments, etc.).</li><li>Experience in preforming process and product audit.&bull; Ability to investigate quality problems using technical judgment to perform root cause analysis, develop and implement effective countermeasures.</li><li>Good understanding of Specific Requirements of Stellantis and Volkswagen.</li><li>Ability to travel as needed (domestic and international).</li></ul>Preferred Qualifications<ul><li>Lean Manufacturing and / or Manufacturing Quality.</li><li>Manufacturing, Process and or Tool Engineering.</li><li>Statistical Problem Solving (Red X, DFSS, DMAIC).</li><li>ISO9001 / IATF 16949 and/or VDA 6.3 Certified Auditor.</li></ul>Physical Requirements and Demands<ul><li>Prolonged periods of sitting at a desk and working on a computer.</li><li>Occasional walking, standing, bending, and reaching.</li><li>Repetitive movement of hands and fingers- typing and or writing.</li></ul>Work Authorization<ul><li>Must be authorized to work in the U.S.</li></ul>Job Type: Full-timePay: From $70,000.00 per yearBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Employee assistance program</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Paid time off</li><li>Vision insurance</li></ul>Application Question(s):<ul><li>Will you now or in the future require job sponsorship to work in the US?</li><li>What is your desired compensation?</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Ability to Commute:<ul><li>Pontiac, MI 48341 (Required)</li></ul>Ability to Relocate:<ul><li>Pontiac, MI 48341: Relocate before starting work (Preferred)</li></ul>Work Location: In person

Supplier Quality Engineer

Elevator Controls

<div>Supplier Quality Engineer
Full Time Position
Sacramento &ndash; Onsite
If you are a motivated problem-solver with a passion for quality and an interest in manufacturing, we have an opportunity for you! Vantage Elevation is seeking a Supplier Quality Engineer to join our Elevator Controls team. In this role, you will support quality activities that help ensure our elevator products meet the highest safety, reliability, and performance standards. Working closely with experienced engineers and production teams, you will gain hands-on experience in inspections, process improvements, and supplier collaboration while building a strong foundation for your career in quality engineering.
About Us
Vantage Elevation, LLC is North America&rsquo;s leading independent manufacturer of elevator components and systems. Vantage is comprised of eight business units including GAL Manufacturing; GAL Canada; Hollister-Whitney; Elevator Controls; Courion; Bore-Max; Thames Valley Controls and Vertical Dimensions. Through its brands, Vantage supplies almost all electro-mechanical devices used in contemporary elevators. Founded in 1927, the Vantage group employs over 900 staff in multiple locations across the United States, Canada, and United Kingdom.
Job Summary
We are seeking an enthusiastic Supplier Quality Engineer to join our elevator manufacturing team in Sacramento. In this role, you will support day-to-day quality activities, assist in resolving supplier and production issues, and help maintain compliance with company and industry quality standards. You will collaborate with engineers, production teams, and suppliers to collect and analyze data, perform inspections, and contribute to process improvements. This position offers hands-on experience in manufacturing quality practices and the opportunity to develop your technical skills while supporting safe, reliable, and high-performing elevator products.
Key Responsibilities<ul><li>
Assist in the supplier qualification and approval process by supporting audits, assessments, and basic risk evaluations.</li><li>
Conduct inspections of incoming materials and components to verify conformance to specifications.</li><li>
Support data collection and maintenance of supplier performance metrics and scorecards.</li><li>
Participate in root cause analysis and corrective/preventive action (RCA/CAPA) activities under the guidance of senior engineers.</li><li>
Assist in documenting and updating quality control procedures and work instructions.</li><li>
Collaborate with cross-functional teams, including Sourcing, Engineering, and Production, to address basic quality issues and implement process improvements.</li><li>
Help prepare quality reports, inspection records, and other documentation for internal and supplier communications.</li><li>
Monitor and track nonconformance reports and follow up with suppliers as directed.</li><li>
Support supplier and internal quality initiatives to meet safety, reliability, and compliance requirements.</li><li>
Travel occasionally to supplier or customer locations as needed (typically less than 10%).</li></ul>
Qualifications<ul><li>
Bachelor&rsquo;s degree in engineering, manufacturing technology, or a related technical field (or equivalent combination of education and relevant experience).</li><li>
Up to 2 years of experience in quality engineering, manufacturing, or a related technical role (internships, co-ops, or project-based experience encouraged).</li><li>
Basic understanding of quality principles, inspection methods, and common manufacturing processes.</li><li>
Familiarity with fundamental quality tools (e.g., basic FMEA, SPC charts, 5 Whys, fishbone diagrams); willingness to learn advanced tools such as PPAP, APQP, and MSA.</li><li>
Exposure to or coursework in ISO 9001 or other quality management standards.</li><li>
Strong problem-solving skills with the ability to collect, organize, and analyze data.</li><li>
Proficient in Microsoft Office Suite; experience with ERP or quality management software is a plus.</li><li>
Strong communication and teamwork skills, with the ability to collaborate across departments.</li><li>
Willingness to travel occasionally (typically less than 20%) to supplier or customer sites.</li></ul>
Benefits of Working With Us<ul><li>
Salary Range for Sacramento based Applicants: $ $73,000 - $92,000 per year (actual compensation will be determined based on experience, location, and in keeping with local legislation).</li><li>
Medical/Dental/Vision/Life Insurance</li><li>
10 Vacation days and 5 sick days with 7 paid holidays</li><li>
HSA</li><li>
401(K)/ Company Match/ Non-Elective</li><li>
Tuition Reimbursement</li><li>
Employee Assistance Program (EAP)</li><li>
&hellip; and more!</li></ul>
Position Details
Full-Time
8:00 AM &ndash; 4:30 PM, Monday - Friday
Sacramento
Vantage Elevation, LLC provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to 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. 
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Like What You Read?
If you&rsquo;re excited by the prospect of supporting manufacturing operations and contributing to a world-class employer, then we invite you to apply for the Quality Engineer position at Vantage Elevation, LLC.
#LI-JM1 
#LI-ECC</div>

Vast

<div><div>At Vast, our mission is to contribute to a future where billions of people are living and thriving in space. We are building artificial gravity space stations, allowing long-term stays in space without the adverse effects of zero-gravity. Our initial crewed space habitat will be Haven-1, scheduled to be the world's first commercial space station when it launches into low earth orbit in May 2026. Our team is all-in, committed to executing our mission safely and on time. If you want to work with the most talented people on Earth furthering space exploration for humanity, come join us.</div>
Vast is looking for a Supplier Quality Engineer, reporting to the Manager of Quality Assurance, to support the development of systems that will be required for the design and build of artificial-gravity human-rated space stations. In the role of Supplier Quality Engineer you will be crucial in ensuring the consistent quality and reliability of the products and components we receive from our suppliers.

This will be a full-time, exempt position located in our Long Beach location.

Responsibilities:
<ul>
<li>Evaluating and onboarding new suppliers, ensuring they meet our quality expectations by conducting regular audits, assessments, and evaluations to ensure that our suppliers adhere to our quality standards.</li>
<li>Assure supplier understanding of product and submission requirements</li>
<li>Establish and maintain strong relationships with our suppliers, address any quality-related issues, identify risks in the supply chain, and implement improvements.</li>
<li>Work collaboratively with design engineers to gain an in-depth knowledge of piece part, assembly, and/or sub-system design intent.</li>
<li>Work collaboratively with various departments across the business to strategically source parts matched with supplier competencies by reviewing and assessing supplier manufacturing processes and quality systems.</li>
<li>Setting and enforcing quality standards for incoming materials, components, and products.</li>
<li>Conduct inspections, tests, and assessments to ensure that the products meet our specifications and are free from defects.</li>
<li>Use expertise to contribute to the prevention of defects and non-conformities, ultimately reducing the likelihood of recalls and/or customer complaints.</li>
<li>Drive continuous improvement initiatives, both internally and with our suppliers, by analyzing quality data, identifying trends, and implementing corrective and preventive actions to enhance the overall quality of our products and reduce costs.</li>
<li>Create and define supplier technical and quality requirements based on customer and program requirements and expectations for NPI and manufacturing phases</li>
<li>Implement and monitor production part approval process (PPAP) with selected suppliers to enable rate manufacturing</li>
<li>Develop and approve process controls to regulate acceptance of critical characteristics</li>
<li>Recommend technical product improvements to reduce risk and potential defect opportunities and provide feedback as appropriate on manufacturing methods and technologies.</li>
<li>Analyze supplier quality and delivery metrics to identify trends, pinpoint systemic performance gaps, and determine root causes in order to develop supplier improvement plans.</li>
<li>Function as liaison between purchasing, engineering, manufacturing and suppliers to resolve supplier quality issues and to provide technical support.</li>
<li>Drive supplier corrective actions associated with any escapes or contaminants identified in Vast manufacturing or the Vast supply chain.</li>
<li>Demonstrate autonomy, innovation, technical excellence, and attention to detail.</li>
</ul>
Minimum Qualifications:
<ul>
<li>Bachelor's degree in engineering, business, or supply chain; or (5+ years of continuous experience in Supplier Quality)</li>
<li>3+ years of manufacturing, mechanical, supply chain, or business management experience</li>
</ul>
Preferred Skills &amp; Experience:
<ul>
<li>Master's degree in engineering, business, or supply chain</li>
<li>5+ years of experience with mechanical assemblies, materials and processes.</li>
<li>1+ years of experience with optical systems.</li>
<li>In-depth understanding of aerospace industry regulations and standards.</li>
<li>Experience managing external suppliers.</li>
<li>Strong negotiating skills to drive preferred pricing and results.</li>
<li>Experience with Quality Management Systems (ISO 9000 / AS9100 / NADCAP).</li>
<li>Knowledge of supplier quality processes (PPAP, APQP, FAI reports, etc.).</li>
<li>Experience in statistical controls and methods (e.g. MSA, GR&amp;R, Design of Experiments, Six Sigma, etc.)</li>
<li>Ability to thrive in a fast paced environment.</li>
<li>Effective written, verbal and presentation communication skills.</li>
</ul>
Additional Requirements:
<ul>
<li>Willingness to work evenings and/or weekends to support critical mission milestones</li>
<li>Ability to lift up to 25 lbs unassisted</li>
<li>Ability to travel up to 50% of the time</li>
</ul>
Pay Range:
<ul>
<li>Quality Engineer II: $100,000- $128,380</li>
<li>Senior Quality Engineer: $126,200 - $150,920</li>
</ul><div><div>COMPENSATION AND BENEFITS</div>
<div></div>
<div>Base salary will vary depending on job-related knowledge, education, skills, experience, business needs, and market demand. Salary is just one component of our comprehensive compensation package. Full-time employees also receive company equity, as well as access to a full suite of compelling benefits and perks, including: 100% medical, dental, and vision coverage for employees and dependents, flexible paid time off for exempt staff and up to 10 days of vacation for non-exempt staff, paid parental leave, short and long-term disability insurance, life insurance, access to a 401(k) retirement plan, One Medical membership, ClassPass credits, personalized mental healthcare through Spring Health, and other discounts and perks. We also take pride in offering exceptional food perks, with snacks, drip coffee, cold drinks, and dinner meals remaining free of charge, and lunch subsidized as part of Vast's ongoing commitment to providing high-quality meals for employees.</div>
<div>
U.S. EXPORT CONTROL COMPLIANCE STATUS
The person hired will have access to information and items subject to U.S. export controls, and therefore, must either be a &quot;U.S. person&quot; as defined by 22 C.F.R. &sect; 120.62 or otherwise eligible for deemed export licensing. This status includes U.S. citizens, U.S. nationals, lawful permanent residents (green card holders), and asylees and refugees with such status granted, not pending.</div> 
<div></div>

EQUAL OPPORTUNITY
<div>
Vast is an Equal Opportunity Employer; employment with Vast is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.</div></div></div>

Sentec

<div>The Supplier Quality Engineer (SQE) ensures the reliability, compliance, and superior performance of supplied components and assemblies, with a heavy emphasis on electromechanics and injection molding. The SQE works closely with Procurement, Quality Assurance, Engineering, and external suppliers to improve quality, optimize processes, and meet stringent industry standards.
Essential Duties and Responsibilities<ul>
<li>Lead the evaluation, qualification, and selection of new and existing suppliers through audits, assessments, and risk-based analysis.</li>
<li>Review and approve supplier manufacturing processes, focusing on electromechanical assembly and molding parameters.</li>
<li>Plan, schedule, and conduct supplier audits to evaluate compliance with quality management systems, regulatory standards, and contractual requirements.</li>
<li>Partner with the Quality team on the inspection and testing of incoming materials, components, and products, ensuring conformity to specifications and regulatory requirements, ensuring timely resolution of any discrepancies or non-conformances with suppliers.</li>
<li>Lead investigations of supplier-related quality issues, utilizing root cause analysis tools to drive effective corrective (CAR) and preventive actions (PAR). Track and report the status of actions related to nonconforming materials or processes (NCPs) to ensure timely closure.</li>
<li>Develop and monitor key performance indicators (KPIs) for supplier quality, delivery, and responsiveness. Generate supplier scorecards and lead regular performance reviews, driving improvement initiatives as necessary.</li>
<li>Maintain documentation of supplier quality activities and support compliance with relevant standards and audits.</li>
<li>Ensure supplier compliance with regulatory and quality standards, including FDA 21 CFR Part 820, ISO 13485, QMS, and GMP requirements.</li>
<li>Partner with Procurement, Quality Assurance, R&amp;D and Engineering to ensure supplier quality requirements are integrated throughout the product lifecycle.</li>
</ul>Requirements<ul>
<li>Bachelor&rsquo;s degree in Mechanical, Electrical, Manufacturing Engineering, Materials Science, or related field.</li>
<li>3-5 years&rsquo; experience in supplier quality engineering, preferably in electromechanics or injection molding industries.</li>
<li>Experience in medical device development and manufacturing environment, preferred.</li>
</ul>Benefits<ul>
<li>Meaningful work in a rapidly growing company with opportunity for advancement</li>
<li>Directly influence the quality of products and make a difference for patients worldwide</li>
<li>Opportunities for professional and personal growth</li>
<li>Base salary: $80,000 - $100,000 plus bonus</li>
</ul>Sentec offers competitive benefits like Medical, Dental, Vision, HSA, FSA, and 401K matching, as well as paid parental leave , a wellness stipend and tuition reimbursement. Sentec emphasizes employee voices and recognizes hard work making it a promising environment for professional growth. Sentec focuses on delivering impactful healthcare products and improving patient care.
By choosing a career at Sentec, you&rsquo;re not just choosing a job &ndash; you&rsquo;re embracing the chance to make a real impact, contributing to the development of innovative medical solutions that support the wellbeing of individuals worldwide.
Sentec is a Swiss-American medical device company specializing in respiratory care. Since its founding in 1999, Sentec utilizes a deep-tech approach that is founded on advanced science and avant-garde technologies for respiratory patients across care areas. Sentec provides healthcare professionals worldwide with non-invasive, continuous monitoring and effective therapeutic solutions.</div>

Unify Technologies

Job Description &amp; Skill Requirement:<ul><li>Knowledge of application of Regulatory requirement including ISO 13485, FDA and International</li></ul>requirements<ul><li>Enhanced quality system requirements (QSR) throughout business unit by improving quality</li></ul>process and CAPA Closure<ul><li>Implementing SICR- Supplier Initiated Change Requests (DCR, ECR, MCR) through Change</li></ul>management Process and as per ISO 13485 &amp; CFR 21 Part 820 requirements<ul><li>Presenting Supplier Initiated Change Requests to Change Management Board (CMB) for review &amp;</li></ul>Approval<ul><li>Review and Closure of Supplier Audit Non-Conformities as per NC &amp; CAPA management System</li></ul>(Track wise)<ul><li>Review of Supplier deliverables like MSA, SPC, GD&amp;T, Process Validation, PPAP, FMEA etc.</li><li>Conducting Supplier's Pre-Assessment Audits with Sourcing &amp; RAQA Leads.</li><li>Implementing Change Control Agreement (CCA), Audit Adoption, Self-Assessment Audit and</li></ul>Onsite Audit through organization procedure<ul><li>Collaborates with cross-functional and suppliers' teams to address top quality issues.</li><li>Own identified supplier driven non-conformances and manage the timely closure of NC's within</li></ul>Trackwise.<ul><li>Own or support identified supplier CAPAs and manage to timely root cause investigation,</li></ul>implementation and closure.<ul><li>Communicate &amp; collaborate with suppliers regarding non-conformances, escalating supplier</li></ul>corrective action requests as required.<ul><li>Participates and may lead in the creation and/or review of new or modified procedures.</li><li>Maintain KPIs for monitoring of supplier quality processes, perform analysis, and interpret trends,</li></ul>identifying and activating on appropriate actions as necessary.<ul><li>Applies statistical methods of analysis and process control to external operations.</li><li>Support manufacturing transfers to/from other plants/facilities, executing appropriate quality</li></ul>activities.<ul><li>Lead quality issues with suppliers &amp; partner with Internal Customers; Lead effective supplier</li></ul>containment and corrections/corrective actions<ul><li>Act as point of contact for Internal/ External Customer groups on key compliance issues related to</li></ul>assigned suppliers<ul><li>Responsible for accuracy and integrity of supplier data that ensures compliance with documented</li></ul>procedures &amp; processes.<ul><li>Ownership and reporting on all quality issues associated with the assigned suppliers. Ensure all</li></ul>assigned supplier related material quality issues are effectively communicated to key stakeholders.<ul><li>Maintain structured communication channels with strategic sourcing, identifying responsibility by</li></ul>commodity / supplier.<ul><li>Deliver continuous improvement activities focusing on supplier quality.</li><li>Participate in supplier audit program - planning, execution and closure.</li><li>Partner with SQM functions and Strategic Sourcing on the developments and approval quality</li></ul>assurance agreements with suppliers.<ul><li>Ability to collaborate effectively with lead cross functional team</li></ul>Qualification:<ul><li>Bachelor's Degree in Engineering or Science-related field</li><li>5+ years' experience in quality, engineering, manufacturing, or highly regulated environment</li><li>Fluent in written, oral in English and</li><li>Understanding of US and International Medical Device Regulations.</li><li>Strong knowledge of Quality Concepts (e.g. Risk Management, NC/CAPA, Audits, Statistics).</li></ul><ul><li>Must possess strong communication, project management and influencing skills as well as have</li></ul>the ability to manage multiple tasks simultaneously.<ul><li>Strong interpersonal skills, written, oral communication and negotiations skills.</li><li>Strong in critical thinking and &quot;outside the box&quot; thinking.</li><li>Highly developed problem-solving skills. Strong analytical skills.</li><li>Demonstrated ability to work independently and as part of cross-functional teams</li></ul>FrenchJob Type: Full-timePay: $73,732.33 - $84,795.92 per yearWork Location: In person

TTM Technologies

<div>TTM Technologies, Inc. &ndash; Publicly Traded US Company, NASDAQ (TTMI) &ndash; Top-5 Global Printed Circuit Board Manufacturer
<h2 class="jobSectionHeader">About TTM 
</h2> 
TTM Technologies, Inc. is a leading global manufacturer of technology solutions including engineered systems, radio frequency (&ldquo;RF&rdquo;) components and RF microwave/microelectronic assemblies, and quick-turn and technologically advanced printed circuit boards (&ldquo;PCBs&rdquo;). TTM stands for time-to-market, representing how TTM's time-critical, one-stop manufacturing services enable customers to shorten the time required to develop new products and bring them to market.
Additional information can be found at www.ttm.com
Summary:
Performs quality assurance activities concerned with the engineering of products, materials and processes by performing the following essential duties.
Essential Duties &amp; Responsibilities:
<ul><li>Performs and evaluates First Article Inspection of Supplier product and approves AS9102 First Article documentation
</li><li>Schedules and performs on-site Surveys and Source Inspections at Supplier&rsquo;s facilities for compliance to Purchase Order requirements
</li><li>Answers questions relating to standard practices and procedures
</li><li>Reviews and provides input to statements of work for subcontractors
</li><li>Acts as liaison between departments and makes independent decisions to insure adherence to quality procedures
</li><li>Develops, implements, and maintains supplier quality procedures
</li><li>Develops and maintains monthly program status
</li><li>Collects data for metrics reporting and analyzes results of activities for potentially adverse trends
</li><li>Prepares status reports for management
</li><li>Generates supplier notifications (NOE, SCR &amp; SCAR) and tracks responses to closure
</li><li>Establishes and maintains an effective monitoring program, including the use of PC-based tools for planning, tracking and evaluating performance
</li><li>Establishes and maintains supplier rating system, approved supplier list, supplier control program, and monthly reports on status of vendors with low ratings
</li><li>Reviews and approves purchase requisitions, purchase orders, and supplier corrective action
</li><li>Performs pre-award surveys as a team member with other departments
</li><li>Generates inspection alerts
</li><li>Minimum 25% travel required
</li><li>Performs other duties as directed
</li></ul>Skills:
<ul><li>Bachelor&rsquo;s degree in Engineering from a four-year college or university
</li><li>Must have a background that would permit the U.S. Department of Defense to issue a secret clearance when necessary for work on a project that requires such a clearance
</li><li>Ability to use standard electronic test equipment, such as oscilloscopes, meters, counters, frequency meters, logic analyzers, etc.
</li><li>Ability to use mechanical measurement equipment, such as calipers, micrometers, height gauges, comparators and scales
</li><li>Knowledge of various drawing types, specifications and Configuration Management systems
</li><li>Knowledge of IPC-A-610, IPC/WHMA-A-620, J-STD-001 requirements in a capacity to make nonconforming material decisions
</li><li>Detailed knowledge of ISO9001/AS9100 and AS9102 requirements
</li><li>Familiarity with the PC (Excel, Word, Power Point)
</li><li>Working knowledge of true Root Cause &amp; Corrective Action Techniques (5 Why, Fishbone, Is/Is Not and 8D tools)
</li><li>Knowledge of Manufacturing processes for Electronics and/or Mechanical assemblies.
</li><li>Knowledge of Advanced Quality Planning (APQP) / Control Plans
</li><li>Knowledge of basic Failure Mode and Effect Analysis
</li><li>Knowledge of Process and Compliance Auditing
</li><li>Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
</li></ul>#LI-PG1 
<h2 class="jobSectionHeader"> 
Compensation and Benefits:
</h2>TTM offers a variety of health and well-being benefit programs. Benefit options include medical, dental, vision, 401k, flexible spending and health savings accounts, accident benefits, life insurance, disability benefits, paid vacation &amp; holidays. Benefits are available on the 1st of the month following date of hire. For some positions, only PTO and holiday benefits are offered.
Compensation ranges for roles at TTM Technologies varies depending on a wide array of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At TTM Technologies, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on each individual set of circumstances. A reasonable estimate of the current range is:
$104,982 - $184,624
Additional compensation: An annual or quarterly company bonus may apply based on position assignment. Positions hired for alternative shift may be eligible for a shift premium based on the assigned shift and location.
Export Statement:
 
Must comply with TTM Export Control Policies and Procedures and all applicable laws including ITAR, EAR and OFAC including but not limited to: a) being able to identify ITAR product on the manufacturing floor and understand that access to these products and related technical data is restricted to only US Citizens and US Permanent Residents; b) recognition of Foreign Person visitors by badge differentiation; c) understand and follow authorization procedures for bringing foreign visitors into facilities (VAL); d) understand the Export and ITAR requirements for shipments leaving the US; e) manage vendor approvals for ITAR manufacturing and services.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status.</div>

MB&A

Contract Supplier Quality Engineer (Onsite &ndash; Orthopedic Medical Device, Spine Preferred)Contract: 8 months (1099 Contractor &ndash; not C2C)Location: Onsite &ndash; Olive Branch, MS or Denver, CO SuburbOverview:We are seeking an experienced Contract Supplier Quality Engineer to support a manufacturing transfer project in the orthopedic medical device industry (spine preferred). This role requires hands-on expertise in supplier quality engineering, process validations, and control plans, with strong working knowledge of MSA &amp; GR&amp;R specific to regulated environments.Key Responsibilities:<ul><li>Support supplier quality activities for manufacturing transfers of orthopedic devices</li><li>Lead and document process validation activities (IQ, OQ, PQ) in compliance with FDA and ISO 13485 standards</li><li>Develop and implement supplier control plans to ensure product quality and consistency</li><li>Execute MSA &amp; GR&amp;R studies for measurement system validation</li><li>Partner with suppliers and internal engineering teams to drive issue resolution</li></ul>Qualifications:<ul><li>5+ years&rsquo; experience in supplier quality or manufacturing transfer within the orthopedic medical device industry (spine preferred)</li><li>Strong knowledge of FDA, ISO 13485, and orthopedic device regulatory requirements</li><li>Expertise in process validations, MSA &amp; GR&amp;R</li><li>Excellent communication, supplier management, and problem-solving skills</li><li>Required onsite full-time in Olive Branch, MS or Denver, CO suburb</li></ul>Job Type: ContractPay: $60.00 - $65.00 per hourApplication Question(s):<ul><li>Tell us about your experience supporting a manufacturing transfer in the medical device industry (ideally orthopedics). What was your role, and what challenges did you face?</li><li>Describe a time when you led or supported process validations (IQ, OQ, PQ). How did you ensure compliance with FDA and ISO 13485 requirements?</li></ul><ul><li>How have you developed and implemented control plans with suppliers to ensure product quality during a transfer? Can you give a specific example?</li></ul><ul><li>Explain your hands-on experience with Measurement System Analysis (MSA) and Gage R&amp;R. How did your work impact the outcome of the project?</li></ul><ul><li>This role is offered as a 1099 contract. Can you confirm your ability and willingness to work on a 1099 basis?</li><li>Are you open for this onsite role, either in Olive Branch, MS or Denver, CO Suburb? </li><li>Are you a Green Card Holder or US Citizen? </li></ul>Work Location: In person

Contract Supplier Quality Engineer

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