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quality engineer

Amphenol

<p></p><div><div><div><div><div><div><div><div><div><div><div><div><p><b>Location:</b></p><b> </b></div></div><div>Yocumtown, Pennsylvania
</div></div><br>
<div><div><div><p><b>Department:</b></p><b> </b></div></div><div>Engineering
</div></div><br>
<div><div><div><p><b>Posted:</b></p><b> </b></div></div><div>8/25/2025
</div></div><br>
<div><div><div><p><b>Location Name:</b></p><b> </b></div></div><div>Valley Green
</div></div><br>
</div></div></div><div><div><div><div><div><div><p><b>Wage:</b></p><b> </b></div></div><div>Depends on Experience<br>
</div></div><br>
<br>
</div></div></div></div></div><p></p><div><div><div><p><b>Position: Quality Engineer</b></p>
<p><b>Location: Valley Green, PA</b></p>
<p>Amphenol High Speed Products Group is the market leader for high speed, high bandwidth electrical connectors for the Telecom/Datacom market (Mobile Networks, Storage, Servers, Routers, Switches, etc.). Our products help to enable the electronics revolution and remain a key enabler for all the major Tier 1 OEM's globally. Our global headquarters are located in Nashua, NH and we have design, sales and manufacturing locations globally. The HSIO CN team is looking for a Quality Engineer to join them in the Valley Green, PA location. The Quality Engineer will help to plan and facilitate quality related activities for manufacturing development projects by fulfilling the duties associated with FMEA's, Product Quality Planning, Process Qualification Planning, Metrology Planning, Control Plans, Inspection Plans and Methods, Workmanship Standards, DOE's and other necessary studies within a development protocol in developing Statistical Process Control.</p>
<p><b>RESPONSIBILITIES:
</b></p><ul><li>Act as a team member to manage projects to assess quality aspects, report process feasibility &amp; risks and make quality recommendations on how to proceed.</li>
<li>Participate in definition of respective project plan qualification tasks and schedules for development projects that meet time to market (TTM) objectives.</li>
<li>Interface with vendors, process engineering, product engineering and manufacturing to assure capability levels and documentation compliance are achieved in meeting quality deliverables.</li>
<li>Participate in quality readiness at the site by providing the inspections plans, metrology, Cpk requirements and any special qualification requirements.</li>
<li>Participated in product &amp; process FMEA, characterization of product and process critical features and respective risk assessment activities.</li>
<li>Determine initial inspection methods based or best-known methods (where applicable) and manage metrology requirements (internal &amp; external)</li>
<li>Define process qualification plans, inspection plans, inspection workflow, metrology requirements and workmanship standards for process engineering.</li>
<li>Facilitate process qualification planning assuring conformance to standards and specifications.</li>
<li>Develop, facilitate and control standards and methods both internally and externally for the inspection of CTF's inclusive of accuracy, linearity, R&amp;R's, long term stability, FAI's, Cmk's and Cpk's.</li>
<li>Support the analysis of defined risk areas and experimentation, proof of principle tooling, feasibility studies, capability studies, detailed design and analysis, DOE, passive data collection (PDC) and or basic technology searches and development.</li>
<li>Assist process development engineers and mechanical Integrity engineers in the (data &amp; statistical) analysis of feasibility studies, DOE's, passive data collection's (PDC) and capability studies.</li>
<li>Assist product and process engineering in the reconciliation of First Article Inspections, Capability Studies and Comparison Studies through corrective actions driven by root cause analysis that incorporate process improvement tools.</li>
<li>Work with outside consulting houses as an extension of the engineering department.</li>
<li>Interface with site quality, engineering, and other departments throughout final phases of development and pre-release to manufacturing.</li>
<li>Transfer all quality pertinent documentation to the receiving manufacturing site.</li>
<li>Coordinate and or participate in the metrology transfer and training to respective personnel.</li></ul><br>
<p>
</p><p><b>QUALIFICATIONS:
</b></p><ul><li>Bachelor's degree from four-year College in engineering, Quality Assurance; or six to eight years related experience and/or training; or equivalent combination of education and experience.</li>
<li>Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations.</li>
<li>Ability to write reports, business correspondence, and procedure manuals.</li>
<li>Ability to effectively present information and respond to questions from groups of managers, customers, and the internal Amphenol groups.</li>
<li>Ability to effectively identify and eliminate common cause variation within continuous or batch processes through the use of solid practices and analysis in establishing statistical process control (SPC)</li>
<li>Ability to define and generate Quality Plans, Control Plans and Workmanship Standards.</li>
<li>Ability to provide qualification assessments related to product/process risks, capability and manufacturability.</li>
<li>Ability to effectively present information and respond to questions from managers, customers, vendors, engineers and manufacturing site representatives.</li>
<li>Should have knowledge and skills using:
<ul><li>Microsoft Suit (Power Point, Excel, Word, SharePoint)</li>
<li>Measurement System Analysis</li>
<li>Statistical analysis software (Minitab)</li>
<li>Geometric Dimensioning &amp; Tolerancing</li>
<li>Strong Knowledge of Gage Repeatability and Reproducibility</li>
</ul></li><li>Demonstrated skill and knowledge to train individuals and teams.</li>
<li>Demonstrated ability to operate with minimal supervision and provide updates on project status where issues or problems can be reviewed, discussed and resolved.</li>
</ul>
<p>Amphenol Corporation is proud of our reputation as an excellent employer. Our focus is to provide the highest level of support and responsiveness to both our employees and our customers, the world's largest technology companies. Amphenol Corporation offers the opportunity for career growth within a global organization. We believe that Amphenol Corporation is unique in that every employee, regardless of his or her position, has the ability to positively impact the business.</p>
<p>Amphenol is an &quot;Equal Opportunity Employer&quot; - Minority/Female/Disabled/Veteran/Sexual Orientation/Gender Identity/National Origin</p>
<p>For additional company information please visit our website at https://www.amphenol-cs.com/</p></div></div></div></div></div></div></div><p></p>

Quality Engineer

Intellectt Inc

<div>
 <p>
  <strong>
   Job Title:
  </strong>
  Quality Engineer (Medical Device)
 </p>
 <p>
  <strong>
   Location:
  </strong>
  Portland, OR
 </p>
 <p>
  <strong>
   Duration:
  </strong>
  06+ Month Contract
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Summary:
  </strong>
 </p>
 <p>
  We are seeking an experienced Quality Engineer to support our client in the medical device industry. This role will be focused on ensuring quality compliance and continuous improvement within extrusion production lines, supporting both manufacturing and product quality requirements.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Provide quality engineering support for extrusion manufacturing processes and production lines.
  </li>
  <li>
   Develop, implement, and maintain quality systems and procedures in compliance with FDA, ISO 13485, and other regulatory requirements.
  </li>
  <li>
   Conduct process validations, risk assessments, and capability studies related to extrusion operations.
  </li>
  <li>
   Partner with cross-functional teams including manufacturing, R&amp;D, and regulatory to support new product introductions and ongoing production.
  </li>
  <li>
   Monitor and analyze non-conformances, deviations, and CAPAs; ensure timely closure with effective corrective and preventive actions.
  </li>
  <li>
   Perform root cause analysis and drive continuous improvement initiatives to enhance product quality and process reliability.
  </li>
  <li>
   Support audits (internal, external, and regulatory) by preparing required documentation and participating in inspections.
  </li>
  <li>
   Provide technical guidance and training to production teams on quality requirements.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Required Skills &amp; Qualifications:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Engineering, Quality, or related technical field.
  </li>
  <li>
   Minimum 3&ndash;5 years of Quality Engineering experience in the medical device industry.
  </li>
  <li>
   Strong background in extrusion manufacturing processes (preferably tubing, catheters, or similar medical device components).
  </li>
  <li>
   Knowledge of FDA 21 CFR Part 11/820, ISO 13485, ISO 14971, and GMP requirements.
  </li>
  <li>
   Experience with process validation (IQ/OQ/PQ), SPC, and statistical data analysis tools (Minitab preferred).
  </li>
  <li>
   Hands-on experience with CAPA, root cause analysis, FMEA, and risk management.
  </li>
  <li>
   Strong problem-solving, analytical, and communication skills.
  </li>
  <li>
   Ability to work effectively in a cross-functional and regulated environment.
  </li>
 </ul>
</div>


Rockford Ball Screw

<div>Description:
<p><b>
Summary/Objective</b></p><p>
The role of the Sr. Quality Engineer is to drive excellence into the product quality and quality processes at RBS though robust quality control inspection processes and effective collaboration with operations. The Quality Engineer will leverage their expertise by fostering a culture of quality in all aspects of the product lifecycle. This position reports directly to the Quality Manager.</p><p><b>
Essential Functions</b></p><p>
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><ul><li>
Perform supplier quality management by collaborating with suppliers to assess and improve their quality systems.</li><li>
Training and development by mentoring and training the QC team, as well as operations associates on the QMS process and general metrology skill sets.</li><li>
Works with RBS 3rd party CMM programming services and oversees the development of efficient CMM part programs and validation.</li><li>
Evaluate and recommend improvement opportunities of existing CMM programs to reduce run time and improve inspection results reporting.</li><li>
Instructs and trains manufacturing personnel on how to properly interpret CMM inspection reports to improve machine utilization, product quality, and production throughput.</li><li>
Maintains Gauge Calibration program ensuring gages are calibrated on time and the appropriate frequencies are established to maximize effectiveness while driving associated costs down.</li><li>
Drives product quality improvement conducting investigations of defective products to determine root causes and the development of corrective actions. Actively maintains RBS RGA and CAR databases.</li><li>
Participates in the development of APQP processes, PPAP&rsquo;s and metrological qualification to improve first time pass.</li><li>
Support quality management with compliance to the company&rsquo;s ISO 9001:2020 quality system through internal audits and promote continuous improvement throughout the organization.</li><li>
Create and/or update RBS QMS documentation when required.</li><li>
Support Quality Management with review of non-conformance/scrap data. Present findings to MRB for dispositioning actions.</li><li>
Any/all other duties as assigned.</li></ul><p><b>
Work Environment and Physical Demands</b></p><p>
Working conditions are normal for a manufacturing environment. Work involves frequent lifting of materials and product up to 50 pounds and seldom lifting to 75lbs. Frequent use of hands and fingers to handle and/or adjust equipment. Moderate reaching, pushing, pulling, gripping, and grasping. Machinery operation requires the use of safety equipment to include but not limited to safety glasses, and steel toed work boots or shoes.</p><p><b>
Position Type and Expected Hours of Work</b></p><p>
This is a full-time position. The standard working hours for exempt employees are set at 45 hours per week with an additional 30-minute lunch break each day. General business hours are 6:30 am- 5:00 pm. this position follows a specific work schedule of Monday through Friday 7:00 am- 4:30 pm. Occasional evening and weekend work may be required to meet business demands.</p><p><b>
Compensation</b></p><p>
Our current hiring pay range for this position is $70,000- $90,000. This hiring pay range is based on several factors which vary based on position. These include labor markets and, in some instances, may include education, work experience, knowledge, skills and certifications.</p><p>
In addition to this base pay, Rockford Ball Screw employees are eligible for a bonus. Depending on your position you may be categorized into different tiers in the quarterly or annual bonus plan. Currently, this position is classified as a Quarterly Bonus within the Individual Contributor tier.</p><p><b>
Benefits</b></p><p>
Rockford Ball Screw believes a happy healthy employee is what makes our business work. We want to continuously invest in the people that make it happen. Rockford Ball Screw eligible employees have access to a comprehensive competitive package. Please visit our website at https://rockfordballscrew.com/contact/careers/ for more information.</p>
Requirements:
<p><b>
Required Education and Experience</b></p><ul><li>
Must be 18 years or older.</li><li>
Associate's Degree in Quality Assurance or a related industrial program or significant relevant work experience.</li><li>
5+ years of experience within quality control in a manufacturing environment practicing ISO 9001.</li><li>
Demonstrated proficiency utilizing metrology/inspection tools, experience with calibration systems.</li><li>
5+ years of experience with CMM operation serving as the SME (Zeiss hardware and/or Calypso Software preferred).</li><li>
Intermediate level of computer literacy, specifically Office 365 (Word, Excel, PowerPoint, and Outlook).</li><li>
Capable of using measuring instruments, i.e. micrometer, calipers, gages, etc.</li><li>
Ability to read/write, perform basic arithmetic, and follow verbal and written instructions.</li></ul><p><b>
Preferred Education and Experience</b></p><ul><li>
Bachelor&rsquo;s degree in quality assurance or a related industrial program.</li><li>
Certification in metal trades industry or Quality Control.</li><li>
Maintenance of Gage Calibration.</li><li>
Control of monitoring and measuring devices.</li><li>
Ability to interpret blueprints with a strong knowledge of GD&amp;T principles and inspection methods.</li><li>
Understanding and application of SPC techniques.</li></ul><p>
It is impossible to list every requirement for, or responsibility of, any position. Similarly, we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.</p></div>

FlexTek

<div>
 <p>
  Quality Systems Engineer - (6-9 month contract)
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Overview:
  </strong>
 </p>
 <p>
  We are seeking an experienced
  <strong>
   Quality Systems Engineer
  </strong>
  to lead the implementation of a robust
  <strong>
   Quality Management System (QMS)
  </strong>
  for our assembly and distribution center. This role is critical in aligning our quality systems with
  <strong>
   ISO 9001 and related standards
  </strong>
  , achieving certification readiness, and embedding a culture of continuous improvement across operations.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   <strong>
    Implement and maintain
   </strong>
   a comprehensive QMS in alignment with
   <strong>
    ISO 9001
   </strong>
   and other applicable standards.
  </li>
  <li>
   Lead the
   <strong>
    ISO certification process
   </strong>
   &mdash;including gap assessments, documentation, training, and audit preparation.
  </li>
  <li>
   Conduct
   <strong>
    internal audits
   </strong>
   to assess compliance and identify opportunities for improvement.
  </li>
  <li>
   Develop and maintain
   <strong>
    quality documentation
   </strong>
   , including policies, procedures, SOPs, and work instructions.
  </li>
  <li>
   Partner with cross-functional teams to
   <strong>
    integrate QMS principles
   </strong>
   into day-to-day operations and processes.
  </li>
  <li>
   Drive
   <strong>
    CAPA (Corrective and Preventive Action)
   </strong>
   activities to resolution and prevent recurrence.
  </li>
  <li>
   Implement and manage a
   <strong>
    Supplier Quality Management System
   </strong>
   , ensuring consistent quality across the supply chain.
  </li>
  <li>
   Facilitate
   <strong>
    QMS training
   </strong>
   for employees to promote awareness and compliance.
  </li>
  <li>
   Continuously monitor system effectiveness and lead
   <strong>
    process improvement initiatives
   </strong>
   .
  </li>
  <li>
   Stay current with changes in
   <strong>
    ISO standards
   </strong>
   and regulatory requirements and ensure continued compliance.
  </li>
  <li>
   Support implementation of industry
   <strong>
    best practices
   </strong>
   and quality tools.
  </li>
  <li>
   Adhere to all
   <strong>
    safety, quality, and compliance standards
   </strong>
   .
  </li>
  <li>
   Perform additional duties as assigned by management.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <p>
  <strong>
   Education &amp; Experience:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in
   <strong>
    Engineering
   </strong>
   ,
   <strong>
    Quality Management
   </strong>
   , or related field
  </li>
  <li>
   Equivalent combination of education and experience may be considered
  </li>
  <li>
   <strong>
    5+ years
   </strong>
   of experience in
   <strong>
    manufacturing
   </strong>
   or
   <strong>
    industrial environments
   </strong>
   , with a focus on quality systems
  </li>
  <li>
   Proven track record of
   <strong>
    implementing QMS from the ground up
   </strong>
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Technical Skills &amp; Certifications:
  </strong>
 </p>
 <ul>
  <li>
   In-depth knowledge of
   <strong>
    ISO 9001
   </strong>
   and other relevant ISO standards
  </li>
  <li>
   Experience with
   <strong>
    internal audits
   </strong>
   , documentation control, and CAPA processes
  </li>
  <li>
   Proficient in
   <strong>
    quality management tools and software
   </strong>
  </li>
  <li>
   Strong analytical and problem-solving abilities
  </li>
  <li>
   Excellent communication skills&mdash;both verbal and written
  </li>
  <li>
   Ability to collaborate across multiple departments and levels of the organization
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Preferred certifications:
  </strong>
 </p>
 <ul>
  <li>
   ASQ Certified Quality Engineer (CQE)
  </li>
  <li>
   ASQ Certified Quality Manager (CQM)
  </li>
 </ul>
 <p>
 </p>
</div>


PEKO Precision Products

<div>
 PEKO Precision Products: We Make Products That Matter
 <br/>
 <br/>
 PEKO is a full-service, debt-free, privately-owned contract manufacturer with over 50 years embedded in the Rochester, NY community. In collaboration with our valued business partners, we deliver new product development (NPI) strategies for product commercialization and provide solutions in the medical, industrial, defense, and renewable energy industries. Enriching life is a crucial component of what we do daily.
 <br/>
 <br/>
 <strong>
  The Opportunity:
 </strong>
 Quality Engineer
 <br/>
 <br/>
 <strong>
  Your Role:
 </strong>
 Under the direction of the Quality Director, you will assist in elevating and systematizing engineering and manufacturing processes. Daily activities will require you to proactively identify potential issues to mitigate risk, improve product quality, manage industry and regulatory compliance and assist in delivering corporate strategic initiatives.
 <br/>
 <br/>
 <strong>
  Responsibilities Include:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Analyzes quality performance data and metrics to identify and drive improvement opportunities.
  </li>
  <li>
   Actively promote and participate in a cross-functional teamwork environment.
  </li>
  <li>
   Facilitate and promote the use of appropriate problem-solving techniques for effective root cause analysis and successful corrective action for customer complaints and internal nonconformances.
  </li>
  <li>
   Understand and promote overall compliance with AS9100/ISO9001 and 13485 specifications as they relate to product conformance and contractual requirements.
  </li>
  <li>
   Understanding of inspection methodologies used to determine compliance for machined and assembled products.
  </li>
  <li>
   Manage, conduct, and support internal and external audits, publishing findings and recommendations.
  </li>
  <li>
   Lead in the implementation of assurances, process controls, and corrective and preventative actions (CAPA) related systems designed to meet or exceed internal and external requirements.
  </li>
  <li>
   Drives continuous improvement and prevention of future failures by helping facilitate the implementation of corrective action.
  </li>
  <li>
   May be accountable for projects/ programs and developing methods and parameters, project methodology, and/ or project proposals.
  </li>
  <li>
   Demonstrate a productive work ethic and commitment to quality that sets the standard for PEKO Standards.
  </li>
  <li>
   Assist with other duties as assigned by the Manager.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Reports To:
 </strong>
 Director of Quality
 <br/>
 <br/>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <strong>
  Basic Qualifications:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Associate degree in Engineering or equivalent.
  </li>
  <li>
   2+ years of quality control experience in a manufacturing environment
  </li>
  <li>
   4+ years of experience utilization of Quality Management Systems (QMS)
  </li>
  <li>
   4+ years of creating and/or managing Design History Files (DHF) and Device Master Records (DMR).
  </li>
  <li>
   Knowledge of ISO 13485 and AS9100; ability to establish quality protocols and procedures that align with requirements.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred Qualifications:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in engineering or equivalent
  </li>
  <li>
   Strong communication, negotiation, team moderation skills, and ability to manage time and workload constraints.
  </li>
  <li>
   Good understanding of QA methodologies, tools, and processes.
  </li>
  <li>
   Knowledge in the application of quality methods and problem-solving tools (TQM, Six Sigma, 8D, 5-Why, Lean Manufacturing, or other continuous improvement methodologies).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Work Authorization:
 </strong>
 US Persons
 <br/>
 <br/>
 <strong>
  PEKO Perks:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive Compensation
  </li>
  <li>
   Tuition Reimbursement (IRS Allowable pre-tax Max)
  </li>
  <li>
   401K, Medical, Dental, Vision
  </li>
  <li>
   Flexible Spending &amp; Health Savings Accounts
  </li>
  <li>
   Life, Short and Long-Term Disability
  </li>
  <li>
   Recognition Awards &amp; Discretionary Benefits
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Our Core Values:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   We care about our talented and loyal PEKO family.
  </li>
  <li>
   We are committed to providing a safe, clean, and positive workplace.
  </li>
  <li>
   We believe in transparency, honesty, and respect for all stakeholders.
  </li>
  <li>
   We are dedicated to maintaining an agile and financially prudent organization.
  </li>
  <li>
   We foster the belief that PEKO people are resilient problem-solvers impacting the future.
  </li>
  <li>
   Get a glimpse of why we are #PEKOProud: #PEKOProud - YouTube
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Other:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This position may require you to follow other job-related instructions and to perform other job-related duties as requested or assigned, subject to all applicable state and federal laws. Duties, responsibilities, and activities may change at any time with or without notice
   <br/>
   <br/>
  </li>
 </ul>
 A reasonable estimate of the compensation range for this position is $60,000 - $89,000 per year.
 <em>
  The wage range for this role considers a wide range of factors when making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational requirements.
 </em>
 .
 <br/>
 <br/>
 Powered by JazzHR
 <br/>
 <br/>
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</div>


Winchester Interconnect

<div><p><b><i>At Winchester Interconnect, we always do the right thing, the right way.</i></b></p><p></p><p><br>
Winchester Interconnect is committed to inspiring the most innovative teams. We foster a dynamic, inclusive environment that thrives on collaboration and continuous growth. We hire exceptional people, celebrate wins, empower employee growth, and provide opportunities to thrive. Winchester is where potential transforms into purpose, and every team member plays a vital role in shaping our shared success.</p><p></p><p><b><br>
Position Summary:</b></p>
<p>
As our Quality Engineer specializing in programming, you will be responsible for product quality verification! Winchester Hermetics is a unique design and manufacturing company that works with cutting-edge technology for the most demanding high-cost-of-failure applications. We support the World's leading Tech companies in a variety of markets using our &ldquo;GSD&rdquo; attitude while still having fun.</p><p></p><p><b><br>
Qualifications &amp; Requirements:</b></p>
<ul>
<li>CMM programming will include Zeiss Calypso software and a strong understanding of GD&amp;T standards (Certifications preferred)</li>
<li>BS degree required and 3-5 years of quality experience</li>
<li>Analytical thinker with demonstrated technical ability to perform root cause analysis, prepare and implement action plans, lead improvement initiatives, and interface with customer&rsquo;s technical resources</li>
<li>Work with drawings, specifications, inspection, and department procedures</li>
<li>Operate and maintain mechanical inspection equipment such as micrometers, pin gages, OGP, and simple electrical and hermeticity testing equipment</li>
<li>Effective use of microscope (10-40x) for inspection of workmanship defects</li>
<li>Document and maintain inspection records</li><br>
</ul>
<p>Our core values - <b>Accountability</b>, <b>Collaboration</b>, and <b>Empowerment</b> <b>(ACE)</b> - are the foundation of how we operate and drive success. You will take ownership of your contributions, collaborate with a team that gets stuff done, and be empowered to innovate and pursue bold initiatives that drive our business forward.</p><p></p><p><b><br>
Are You Our Next ACE?</b></p>
<ul>
<li><b>General QMS</b> - In-process Inspection, final QC, receiving inspection, review FAIs, and maintain control plans</li>
<li><b>Long-Term Organic Growth - </b>Help build talent in the QC team by growing current team members and training new hires, reduction/eliminating RMA&rsquo;s &amp; CAR&rsquo;s, improving inspections, yield, &amp; reducing inventory adjustments</li>
<li><b>A Quality Culture - </b>Champion the Winchester culture while creating a strong department</li>
<li><b>Safety </b>- Support and awareness of safety policies and procedures</li>
<li>Actively participate on behalf of the Quality team both internally and externally on NPI projects, Engineering requirements, contract review, RMA&rsquo;s, CAR&rsquo;s, production, and general customer service</li>
<li>Support the maintenance of inspection criteria and control plans to ensure conformance</li>
</ul>
<p><b>Systems You&rsquo;ll Use:</b></p>
<ul>
<li>Google Enterprise</li>
<li>BambooHR</li>
<li>Paycom &amp; ADP</li>
</ul>
<p>For a sneak peek into some of our benefits and to learn more about our career opportunities, click here https://www.winconn.com/jobs/.</p><p></p><p><i><br>
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities. In addition to federal law requirements, Winchester Interconnect complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.</i></p><p></p><p><i><br>
Winchester Interconnect expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status.</i></p><p></p><p><b><br>
***Candidate Inquiries Only-No Third-Parties***</b></p></div>

Vast

<div><div><p>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<b> all-in</b>, 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.</p></div><p>
Vast is looking for a <b>Supplier Quality Engineer</b>, reporting to the<b> Manager of Quality Assurance</b>, 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.</p>
<p>
This will be a <b>full-time, exempt</b> position located in our <b>Long Beach</b> location.</p>
<p><b>
Responsibilities:</b></p>
<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>
<p><b>Minimum Qualifications:</b></p>
<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>
<p><b>Preferred Skills &amp; Experience:</b></p>
<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>
<p><b>Additional Requirements:</b></p>
<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>
<p><b>Pay Range:</b></p>
<ul>
<li>Quality Engineer II: $100,000- $128,380</li>
<li>Senior Quality Engineer: $126,200 - $150,920</li>
</ul><div><div><b>COMPENSATION AND BENEFITS</b></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>
<p><b>U.S. EXPORT CONTROL COMPLIANCE STATUS</b></p>
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><br>
<div></div>
<p><b>
EQUAL OPPORTUNITY</b></p>
<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>

Supplier Quality Engineer

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