<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Engineer is responsible for ensuring that products and processes adhere to all standards and requirements. </p><p>The role includes participating in quality-improvement initiatives and projects, performing quality reviews and internal audits, evaluating data, and writing reports to validate or indicate deviations from existing standards. The Quality Engineer analyzes statistical data and product specifications to determine standards and establish quality and reliability objectives of finished products. They will recommend modifications to existing quality or production standards to achieve optimum quality.</p><p><br></p><h2>Responsibilities</h2><ul><li>Recommend quality improvement by identifying statistical methods relevant to manufacturing processes.</li><li>Research statistical confidence by identifying sample size and acceptable error rate, determining levels of confidence.</li><li>Analyze quality data from plant processes or customer indicators.</li><li>Provide feedback to customers based on quality projects (e.g., warranty, APQP, issues, etc.).</li><li>Lead quality investigations and problem solving.</li><li>Research statistical reliability by using mean time before failure, reliability modeling, and reliability demonstration tests.</li><li>Develop quality improvement experiments by applying full and fractional factorial techniques.</li><li>Develop sampling plans by applying attribute, variable, and sequential sampling methods.</li><li>Maintain statistical process controls by applying demerit/unit, zone charting, charts for distributions, and individual-media/range for multi-stream processes.</li><li>Analyze data by completing hypothesis, normal distribution, and process capability analysis tests.</li><li>Prepare statistical information and reports by collecting, analyzing, and summarizing data and trends.</li><li>Contribute to quality engineering and organization success by welcoming related, different, and new requests; helping others accomplish job results.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s Degree in Engineering</li><li>3+ years of Quality Engineering experience in a Manufacturing environment</li><li>Proficient in APQP</li><li>IATF / automotive experience</li><li>Process audit experience</li><li>Proven troubleshooting/root cause analysis</li><li>Statistical analysis</li><li>Statistical process control</li></ul><h2>&quot;Nice to have&quot; Qualifications</h2><ul><li>Statistical analysis</li><li>SPC</li></ul><h2>Work Environment</h2><p>The role offers a high level of project ownership and the opportunity to be considered a leader within the organization. </p><p>You will receive internal training and development from engineering leadership. The company takes pride in promoting from within, providing opportunities to move into advanced roles. </p><p>The position includes 10 days of PTO, 6 paid holidays, and access to Udemy after 6 months (negotiable). </p>

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Quality Engineer

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>The primary objective of this role is to ensure quality in manufacturing and supply chain in support of the development and production of the Aurora Driver, delivering the benefits of self-driving technology safely, quickly, and broadly. A successful candidate is data-driven, excels at complex problem-solving, has a strong quality and product-focused mindset, and can lead cross-functional teams to identify and eliminate quality problems, issues, and risks.</p><br><h2>Responsibilities</h2><ul><li>Create test and inspection plans based on program plans, product requirements, and specifications.</li><li>Coordinate calibration of data acquisition, inspection, and testing equipment, maintaining records and certificates.</li><li>Design or coordinate the design of custom inspection and test fixtures and sensors for quality control.</li><li>Direct and manage all non-conforming product(s) and return material authorization activities.</li><li>Support inspection and testing activities to ensure continuous compliance of products to specifications.</li><li>Collaborate closely with engineering and manufacturing teams to develop manufacturing test requirements, quality standards, and product quality plans.</li><li>Identify critical risks in design and manufacturing and drive actions to mitigate risks with cross-functional teams.</li><li>Develop, validate, and roll out critical quality controls across production lines, in coordination with engineering and manufacturing teams.</li><li>Lead and support the qualification of new production lines and processes by utilizing quality tools and techniques.</li><li>Work with internal and external suppliers to establish requirements and ensure product quality.</li><li>Investigate and resolve product complaints and quality problems in the field and in the process.</li><li>Use lean tools, statistical techniques, and analytical methods for effective problem-solving.</li><li>Track quality performance metrics, prioritize top issues, and drive continuous improvement activities.</li><li>Provide technical support and mentorship to junior-level engineers and technicians.</li><li>Lead and participate in initiatives to support business and quality objectives.</li></ul><h2>Essential Skills</h2><ul><li>Quality Control, QMS, IPC expertise.</li><li>Bachelor of Science in Electrical, Mechanical, Industrial Engineering, or related fields; or equivalent combination of education and experience.</li><li>5+ years in automotive manufacturing, electro-mechanical assembly operations, robotics, or equivalent field experience.</li><li>Excellent data analysis skills, using simulation/modeling tools.</li><li>Ability to interpret regulations and test procedures.</li><li>Ability to operate and use diagnostic scan tools, scopes, meters, and other test equipment.</li><li>Ability to read design/wiring schematics and operate data acquisition systems.</li><li>Understanding of test equipment maintenance, calibration, upgrades, and improvements.</li><li>Investigate, debug, and resolve quality inspection or test problems in the manufacturing process.</li><li>Comprehensive understanding of the quality toolbox (SPC, 8D root cause analysis, tolerancing, control and inspection standards).</li><li>Knowledge of Continuous Improvement, Kaizen, 5S, Six Sigma Process, APQP, PPAP, DFMEA, PFMEA.</li><li>Experience with Google Sheets, Docs, Slides, and Gmail.</li><li>Experienced in ISO-9001.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in IATF, ISO standards.</li><li>Experience with Linux operating systems.</li><li>Minitab or other statistical software capabilities.</li><li>Experience programming and scripting (C++, Python or equivalent).</li><li>Experience with Jira.</li><li>Ability to communicate effectively with internal stakeholders and third parties.</li></ul><h2>Work Environment</h2><p>This is an on-site position where you will be working directly on autonomous vehicles.</p><br>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>This position is responsible for supporting the Quality Team to ensure that products and processes comply with the relevant requirements of the Quality Management System and ISO 9001. The role also involves managing the Quality Management System and driving continuous improvement initiatives across all areas of the company, utilizing Quality tools to guide the process.</p><br><h2>Responsibilities</h2><ul><li>Assist in establishing, implementing, and maintaining the Quality Management System; ensuring integrity of the data.</li><li>Responsible for maintenance and improvement of the Quality Management System.</li><li>Perform root cause analysis and implementation of corrective action for production and operation concerns.</li><li>Support the Quality Team to ensure products and processes comply with relevant requirements of the Quality Management System and ISO 9001.</li><li>Conduct full cycle internal audits; compile and present final determination to management.</li><li>Review and analyze nonconformance reports; deliver insightful recommendations that drive actions to improve the quality of on-time delivery.</li><li>Analyze customer complaints; determine root cause and create corrective and preventative actions.</li><li>Interact and support Purchasing; evaluate external suppliers including conducting on-site audits.</li><li>Perform other duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering</li><li>Quality assurance</li><li>PPAP</li><li>Root cause analysis</li><li>CAPA</li><li>Quality management</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>B.S. or M.S. degree in Engineering, or related study required.</li><li>Experience with quality tools such as CAPA, PDCA, Six Sigma, DFMA.</li></ul><h2>Work Environment</h2><p>The work environment involves using a variety of quality tools and methodologies, such as CAPA, PDCA, Six Sigma, and DFMA, to drive continuous improvements. The role requires interaction with various departments, including Purchasing, and conducting evaluations and audits of external suppliers. Dress code and shift information are not specified.</p><br>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>Join a dynamic team and contribute to precision CNC-machining manufacturing, quality, and automation technology in industries such as aerospace, defense, semiconductor, and oil and energy. We are seeking two Quality Engineers to enhance our growing team.</p><br><h2>Responsibilities</h2><ul><li>Lead a machining team of five, working on the floor to review drawings and blueprints.</li><li>Develop quality plans and apply problem-solving techniques and process improvements.</li><li>Ensure compliance with ISO9001 and AS9100 standards.</li><li>Engage in customer and client communication to address quality concerns.</li><li>Work with the quality team to verify and inspect blueprints and drawings.</li><li>Perform root cause analysis and implement corrective actions.</li><li>Conduct PPAP and audits to ensure quality assurance.</li><li>Train and lead a team of five, focusing on floor operations and contract machining.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering and assurance expertise.</li><li>Proficiency in root cause analysis and PPAP.</li><li>Experience with audits, ISO9001, and AS9100 standards.</li><li>Strong communication skills for interacting with customers, engineers, and vendors.</li><li>4-10 years of relevant experience.</li><li>Experience in aerospace is preferred.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Familiarity with GD&amp;T.</li><li>Ability to work on the floor and understand machining operations.</li><li>Experience in an ITAR facility.</li><li>Soft skills are highly valued.</li></ul><h2>Work Environment</h2><p>The work environment is a machine shop setting, focusing on precision machining with opportunities to work directly on the floor and engage in contract machining. This role emphasizes a combination of technical skills and effective communication, with a strong emphasis on process improvement and quality assurance.</p><br>

<h3>Quality Engineer</h3><p><em>Location: Onsite in Melbourne, FL</em></p><p><em>Industry: Aerospace &amp; Defense </em></p><p><br></p><p>Actalent is seeking a highly experienced Quality Engineer to lead quality assurance efforts across the full lifecycle of satellite system development. </p><p><br></p><p>You’ll play a critical role in ensuring compliance with NASA, DoD, ISO, and AS standards from concept through launch. This is a high-impact position offering autonomy within a collaborative, international engineering environment.</p><p><br></p><h3>Responsibilities</h3><ul><li>Lead quality assurance for satellite programs from design through operational handover.</li><li>Apply and interpret standards such as NASA NPR 8735.2, NASA-STD-8739 series, MIL-STD-1540, and MIL-STD-883.</li><li>Establish and maintain ISO 9001 and AS9100 quality management systems.</li><li>Collaborate with engineering, manufacturing, and test teams to implement quality plans, risk assessments, and process controls.</li><li>Participate in design reviews, technical meetings, and failure investigations.</li><li>Conduct internal, supplier, and system audits aligned with industry standards.</li><li>Define inspection criteria and oversee verification and validation during integration and testing.</li><li>Support root cause analysis and CAPA processes for nonconformances.</li><li>Maintain detailed quality documentation to ensure compliance.</li><li>Mentor junior quality staff and drive continuous improvement initiatives.</li></ul><h3>Qualifications</h3><ul><li>Proven experience in quality engineering for space hardware programs.</li><li>Deep knowledge of NASA, ISO 9001, AS9100, and military standards.</li><li>Expertise in FMEA, PFMEA, FRACAS, and root cause analysis.</li><li>Certified Quality Engineer (CQE) or equivalent certification preferred.</li><li>Experience with spaceflight hardware qualification and acceptance processes.</li><li>Familiarity with configuration management and nonconformance tracking systems.</li><li>Knowledge of ECSS standards is a plus for international programs.</li><li>Strong organizational skills and attention to detail.</li><li>Excellent problem-solving and multi-tasking abilities.</li></ul><h3>Top Skills</h3><p>Quality Engineering | Space Hardware | NASA Standards | ISO 9001 | AS9100 | Environmental Testing | Launch Preparation | FMEA | FRACAS | Root Cause Analysis</p>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>Assure product quality from design through assembly operations. Provide leadership in failure analysis and corrective action to prevent defects from happening in the manufacturing and assembly operations. The Quality Engineer will also serve as a quality representative, providing input on the manufacturability and serviceability of designs. Utilizing failure and defect reports, the role will assist in making recommendations to improve quality.</p><br><h2>Responsibilities</h2><ul><li>Perform failure and defect analysis in cooperation with Engineering and Manufacturing to determine appropriate corrective actions for quality problems and follow-up to ensure these actions are implemented.</li><li>Conduct in-process audits to identify production problems before products are submitted to Final Inspection.</li><li>Plan and execute quality measures for incoming material, manufactured components, assemblies, and finished products.</li><li>Assist in establishing effective inspection sampling plans and quality audits to ensure cost-effective compliance with customer expectations and specifications.</li></ul><h2>Essential Skills</h2><ul><li>3-5 years of experience in quality engineering with a focus on manufacturing quality and process improvement.</li><li>Proficiency in PPAP, root cause analysis, and statistical process control (SPC).</li><li>Strong understanding of quality standards, quality control, and quality assurance.</li><li>Experience in conducting audits and statistical analysis.</li><li>Bachelor&#39;s degree in Engineering or a related field.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Training in SPC and other quality tools used for process improvement.</li><li>Knowledge of SCAR, CAPA, CpK, PPAP, control plans, and non-conformance management.</li></ul><h2>Work Environment</h2><p>The position is based in a clean facility and involves a mix of desk work and on-the-floor activities. The Quality Engineer will have a dedicated desk and will use various tools to manage suppliers and improve supplier performance.</p><br>

<h1><strong>Job Title: Quality Assurance Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Quality Assurance Engineer to join our integration team. This role is pivotal in post-market surveillance, complaint handling, and enhancing quality systems, particularly as we integrate a newly acquired software company into our existing medical device quality system. The ideal candidate will possess experience with software products and non-medical devices, coupled with a robust <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in quality systems.</p><p><br></p><h2>Responsibilities</h2><ul><li>Investigate customer complaints, warranty claims, and field failures.</li><li>Identify root causes and drive corrective actions.</li><li>Improve the product return and complaint handling process.</li><li>Ensure timely resolution of complaints by collaborating with teams.</li><li>Provide regular trend reports to highlight recurring issues.</li><li>Maintain and improve the Quality Management System (QMS).</li><li>Align with standards such as ISO 9001, ISO, and TL 9000.</li><li>Write and update quality procedures and work instructions.</li><li>Collaborate with stakeholders to create process maps for new procedures.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering</li><li>CAPA post-market surveillance</li><li>Complaint handling</li><li>ISO standards compliance</li><li>Corrective action plans</li><li>Non-conforming processes</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Engineering, Life Sciences, or related field (or equivalent experience).</li><li>3+ years in Quality Engineering within a regulated industry (medical devices, pharma, etc.).</li><li>Strong knowledge of ISO and 21 CFR Part 820.</li><li>Experience with complaint handling, CAPA, and nonconformance processes.</li><li>Excellent problem-solving, data analysis, and communication skills.</li></ul><h2>Work Environment</h2><p>The position involves working in a dynamic and fast-paced environment where adherence to quality standards is paramount. The role requires collaboration with various teams to ensure the integration of software products into the medical device quality system is seamless and effective. The work environment encourages proactive problem-solving and innovation in quality improvements.</p>

<h1 style="text-align: center;"><strong>Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>This position is responsible for supporting the Quality Team to ensure that products and processes comply with the relevant requirements of the Quality Management System and ISO 9001. The role also involves managing the Quality Management System and driving continuous improvement initiatives across all areas of the company, utilizing Quality tools to guide the process.</p><p><br></p><h2>Responsibilities</h2><ul><li>Assist in establishing, implementing, and maintaining the Quality Management System; ensuring integrity of the data.</li><li>Responsible for maintenance and improvement of the Quality Management System.</li><li>Perform root cause analysis and implementation of corrective action for production and operation concerns.</li><li>Support the Quality Team to ensure products and processes comply with relevant requirements of the Quality Management System and ISO 9001.</li><li>Conduct full cycle internal audits; compile and present final determination to management.</li><li>Review and analyze nonconformance reports; deliver insightful recommendations that drive actions to improve the quality of on-time delivery.</li><li>Analyze customer complaints; determine root cause and create corrective and preventative actions.</li><li>Interact and support Purchasing; evaluate external suppliers including conducting on-site audits.</li><li>Perform other duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering</li><li>Quality assurance</li><li>PPAP</li><li>Root cause analysis</li><li>CAPA</li><li>Quality management</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>B.S. or M.S. degree in Engineering, or related study required.</li><li>Experience with quality tools such as CAPA, PDCA, Six Sigma, DFMA.</li></ul>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Engineer is responsible for ensuring that production quality standards are met through comprehensive quality assurance activities. This role involves coordination with various departments such as Operations, Customers, Suppliers, Sales, Engineering personnel, Technicians, and Corporate support.</p><p><br></p><h2>Responsibilities</h2><ul><li>Manage the PPAP process by establishing requirements, gathering documentation, validating the process, and obtaining final approval.</li><li>Develop and implement Control Plans and FMEAs.</li><li>Interpret data using CPK and CP methodologies.</li><li>Apply knowledge of the IATF16949 technical standard.</li><li>Establish process controls including Poke yokes and check frequencies.</li><li>Perform layered audits and internal process audits.</li><li>Collaborate with Automotive OEMs through in-person meetings, phone calls, and email communication.</li><li>Understand and interpret blueprint tolerances.</li><li>Utilize measurement tools such as calipers, micrometers, and general hand gauges.</li><li>Operate CMM, Faro arm, or other programmable measurement devices.</li><li>Organize and analyze data to recommend actions to management.</li><li>Implement formal problem-solving techniques such as 5P or 8D.</li><li>Supervise a team of more than four associates across three shifts.</li><li>Work with the production team on continual improvement activities related to cost reduction.</li></ul><h2>Essential Skills</h2><ul><li>3+ years of experience in quality engineering.</li><li>Experience in a fast-paced manufacturing environment.</li><li>Proficiency with measurement tools including calipers, micrometers, and hand gauges.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with machining and/or aluminum products.</li><li>Experience working in casting environments.</li><li>Ford experience is a plus.</li></ul><h2>Work Environment</h2><p>This position offers a dynamic work environment with great benefits and an on-site health clinic. It involves supervision across three shifts, ensuring effective teamwork and coordination. The role requires interaction with advanced measurement technologies and promotes continual improvement activities for cost reduction.</p>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Quality Engineer to join our team. The successful candidate will engage in problem analysis, mistake-proofing countermeasure investigation, and process evaluation. You will play a pivotal role in resolving customer quality concerns and ensuring the implementation of quality standards. This includes developing check fixtures, ensuring the correctness of test methods, and assisting in the development of test fixtures for new programs.</p><br><h2>Responsibilities</h2><ul><li>Analyze problems and investigate mistake-proofing countermeasures.</li><li>Review and evaluate process changes.</li><li>Resolve customer quality concerns by collaborating with Internal QAE, manufacturing, and production engineering personnel.</li><li>Create and implement quality standards such as Key Quality Check Standard, Critical Process Check Standards, and QA data sheets.</li><li>Develop check fixtures and evaluation methods to confirm product quality.</li><li>Ensure test methods, equipment, and programming are correct.</li><li>Assist in developing test fixtures and procedures for new programs and identify continuous improvement ideas.</li><li>Investigate and dispose of product abnormalities in a timely manner.</li><li>Ensure department reports are accurate and distributed timely both within and outside the department.</li><li>Prepare and evaluate new products, ensuring compliance with SRK-OH and customer standards.</li><li>Attend initial builds at customer lines to address concerns and represent our commitment to quality.</li><li>Perform periodic proactive customer visits and communicate with customers regarding quality issues.</li><li>Participate in and support QA Target Management activities.</li></ul><h2>Essential Skills</h2><ul><li>3+ years of practical experience in Automotive Engineering, Engineering Quality, or Manufacturing Quality.</li><li>Proficiency in IATF, PPAP, ISO9001.</li><li>Experience with problem-solving tools, including root cause analysis and statistical analytical tools.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>BS Degree in Engineering is nice to have.</li><li>Automotive QE experience working with Ford, Nissan, or Honda Systems/Portals.</li><li>Experience working directly with automotive OEMs.</li><li>Familiarity with castings, rubber curing, and rubber injection molding.</li></ul><h2>Work Environment</h2><p>The work environment is fast-paced and involves manufacturing anti-vibration automotive components. The products include hydraulic and conventional engine mounts, body mounts, engine drivelines, exhaust isolation mountings, and body isolation products. These products aim to enhance comfort, reduce noise, and improve road handling in vehicles.</p><br>

<h2>Responsibilities</h2><ul><li>Approval of incoming and outgoing products.</li><li>Gauging and some knowledge of CMM programming.</li><li>Adhering to ISO 9001 standards.</li><li>Performing internal audits.</li><li>Reading and interpreting blueprints and GD&amp;T.</li><li>Developing and implementing quality standards.</li><li>Developing and implementing quality control systems.</li><li>Monitoring and analyzing quality performance.</li><li>Inspecting and testing materials, equipment, processes, and products to ensure quality specifications are met.</li><li>Collaborating with operations managers to develop and implement controls and improvements.</li><li>Ensuring that workflows, processes, and products comply with safety regulations.</li><li>Investigating and troubleshooting product or production issues.</li><li>Developing corrective actions, solutions, and improvements.</li><li>Reviewing codes, specifications, and processes.</li></ul><h2>Essential Skills</h2><ul><li>3-5+ years of experience in Quality Engineering.</li><li>Experience developing and implementing quality systems and standards in an ISO 9001 environment.</li><li>PPAP experience.</li><li>Blueprint reading and troubleshooting product or production issues.</li></ul>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>Responsible for a wide range of inspection functions supporting quality operations. This includes reviewing documents, drawings, and specifications, as well as planning to meet quality standards. You will also create manufacturing plans for production and train manufacturing teams (Inspection and Production) to understand customer requirements.</p><br><h2>Responsibilities</h2><ul><li>Perform first article inspections on machined parts using micrometers, calipers, and other measurement devices while working in compliance with AS9100 standards.</li><li>Review planning and work instructions.</li><li>Train quality and production teams to meet customer requirements.</li><li>Utilize precision measurement tools and equipment including calipers, micrometers, height gauges, hardness testers, and conductivity meters.</li><li>Familiarize with outside processing certifications.</li><li>Read and interpret Engineering drawings and models.</li><li>Use Microsoft Office efficiently.</li><li>Apply CATIA/Enovia CAD experience.</li><li>Understand basic CMM operations.</li><li>Understand basic CNC machining.</li><li>Conduct AS9100/QMS audits.</li><li>Implement Six Sigma/8D methodologies and RCCA training.</li><li>Communicate with internal customers.</li><li>Perform assembly inspections.</li><li>Conduct CMM inspections.</li><li>Approve first article inspections (FAI).</li></ul><h2>Essential Skills</h2><ul><li>Minimum of five years’ experience in Quality Aerospace/Aircraft.</li><li>Proficiency in quality engineering and quality assurance.</li><li>Experience with CATIA, blueprint reading, and AS9100 standards.</li><li>Quality inspection experience.</li><li>Proficiency in reading engineering drawings/models.</li><li>Proficiency with Microsoft Office.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Basic understanding of CMM.</li><li>Basic understanding of CNC machining.</li><li>Experience with Six Sigma/8D and RCCA training.</li><li>Familiarity with outside processing certifications.</li></ul><h2>Work Environment</h2><p>This is a full-time position with hours from Monday to Friday, 8 AM to 5 PM, in an engineering office area. The quality department is expanding, and this new role will help manage the increased workload coming into the shop.</p><br>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>As a Quality Engineer, you will play a vital role in supporting activities related to manufacturing quality assurance. This includes managing nonconformance and corrective action systems, supporting new and existing product quality, and conducting root cause investigations. You will collaborate with various teams to ensure product and process compliance with industry standards and regulations.</p><br><h2>Responsibilities</h2><ul><li>Generate corrective action requests and facilitate improvement plans.</li><li>Verify closure of corrective actions and conduct periodic reviews.</li><li>Support the development and maintenance of quality documentation, including control plans and inspection procedures.</li><li>Process Failure Mode and Effects Analysis (FMEA) and support Advanced Product Quality Planning (APQP).</li><li>Lead root cause investigations and implement corrective actions for production quality issues.</li><li>Conduct internal audits to ensure compliance with quality standards.</li><li>Create quality control plans that meet customer, regulatory, and sector requirements.</li><li>Review production specifications to ensure conformance with drawings and contract requirements.</li><li>Establish quality controls over production processes and testing throughout the product cycle.</li><li>Analyze reported defects and failures, approve dispositions, and document corrective actions.</li></ul><h2>Essential Skills</h2><ul><li>Experience with quality assurance and root cause analysis.</li><li>Proficiency in PPAP, corrective action, CAPA, FMEA, and quality assurance processes.</li><li>Familiarity with ISO 9001 and AS9100 standards.</li><li>Experience with internal audits and supporting process flow charts.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in the manufacturing industry.</li><li>Experience with FMEA, APQP, FAI, and Corrective Action.</li><li>Exposure to internal audits is a plus.</li></ul><h2>Work Environment</h2><p>This role is primarily onsite with 75% of the time spent at a desk and 25% on the shop floor. The company, which has around 250 employees, operates in a newly refurbished, bright, and open facility. Benefits include a 401k match and tuition reimbursement, with repayment conditions if leaving within 24 months.</p><br>

<h1 style="text-align: center;"><strong>Hiring for an Aerospace Quality Engineer in Cheshire, CT!</strong></h1><p><br></p><h2>Job Description</h2><p>Join a leading organization in the aerospace and defense industry as a Quality Engineer. You will be responsible for overseeing all quality-related activities, ensuring compliance with Quality Management Systems, and contributing to continuous improvement initiatives. This position offers growth opportunities and the chance to work in a dynamic environment in Cheshire, CT.</p><p><br></p><h2>Responsibilities</h2><ul><li>Ensure processes and procedures defined in the Quality Management System (QMS) are understood and followed to maintain Quality System Approvals.</li><li>Lead and support internal and external audit activities, including System, NADCAP, and Customer audits, to meet requirements and maintain approvals.</li><li>Ensure export compliance by understanding and controlling Export Control requirements.</li><li>Drive the robust Root Cause Corrective Action (RCCA) process with real-time daily stand-up Quality reviews and non-conformance tracking.</li><li>Support process improvements with on-time reporting of Quality Key Performance Indicators (KPIs) and drive year-over-year improvements in quality performance.</li><li>Manage all aspects of the Quality Planning, New Product Introduction (NPI), and First Article Inspection (FAI) processes.</li><li>Review customer purchase orders, requirements, and drawing specifications.</li><li>Conduct ballooned drawings and associated document reviews.</li><li>Perform gaging reviews and manage special gaging requirements.</li><li>Conduct Gage R&amp;R Studies and develop Statistical Process Control (SPC) Plans.</li><li>Create Inspection Management System (IMS) and FAI templates in line with customer requirements.</li><li>Develop and validate Coordinate Measuring Machine (CMM) Programs.</li><li>Secure special process approvals and Non-Destructive Testing (NDT).</li><li>Coordinate customer submittals and approvals, utilizing customer web portals.</li><li>Attend customer training and attain certifications for self-release programs.</li><li>Utilize statistical software to establish, analyze, and address quality process control data.</li><li>Lead regular SPC review sessions with engineering and develop action plans for continuous improvement.</li><li>Participate actively in the Company Continuous Improvement Program and Rapid Improvement Events (RIEs).</li><li>Perform other related duties or responsibilities as required.</li><li>Participate in training as needed.</li><li>Domestic travel up to 5-10% may be required.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s Degree in Engineering or a related field.</li><li>2+ years of experience in a manufacturing environment, aerospace preferred.</li><li>Proficiency in Microsoft Word, Excel, PowerPoint, and Access.</li><li>Working knowledge of inspection techniques and quality engineering practices.</li><li>Understanding of data collection and Statistical Process Control (SPC) techniques.</li><li>Good communication skills, capable of effectively communicating with engineers, shop personnel, management staff, suppliers, and customers.</li><li>Must be a “U.S. Person” as defined by the US Government and able to work without restriction with ITAR-related data.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>5+ years of experience in a manufacturing environment, aerospace preferred.</li><li>Experience with root cause analysis and supplier quality management.</li><li>Familiarity with ISO 9001 standards.</li><li>Experience with gage R&amp;R, NPI, QMS, and airfoil manufacturing.</li><li>Pratt experience is highly preferred.</li><li>Experience with stators, vanes, or airfoils is a plus.</li></ul><h2>Work Environment</h2><p>Enjoy a 9/80 work schedule, offering every other Friday off. Benefit from a profit-sharing program and opportunities for career growth. Medical, dental, and vision benefits start the month following your hire date. Participate in a 401K plan with a company match of up to 4%. Work in state-of-the-art facilities located in Cheshire, CT, equipped with the latest technologies.</p>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>Lead the Quality Review Board process and collaborate with other technical leads to investigate, understand, and resolve customer feedback issues. Work closely with engineering, manufacturing, product management, quality, and supplier quality teams to understand customer and product requirements, design intent, and manufacturing processes to develop root cause of failure. Create, maintain, and report key performance measures (KPIs).</p><br><h2>Responsibilities</h2><ul><li>Lead Quality Review Board process.</li><li>Receive customer feedback and collaborate with other technical leads to resolve issues.</li><li>Collaborate with engineering, manufacturing, product management, quality, and supplier quality teams to understand requirements and develop root cause of failure.</li><li>Create, maintain, and report key performance measures (KPIs).</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering</li><li>Problem solving</li><li>Root cause analysis</li><li>Bachelor&#39;s degree in Mechanical Engineering or related field</li><li>2+ years of related quality engineering experience</li><li>Experience working with customers or suppliers</li><li>Six Sigma</li><li>8D problem solving</li><li>Project management</li><li>Process engineering</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>5+ years of experience in a manufacturing setting preferred</li><li>Process Engineering experience is a plus</li><li>Refrigeration experience would be a plus</li><li>Strong problem-solving and analytical capability</li><li>Detail-oriented</li><li>Ability to assess product performance and develop root cause analysis and initial problem solving</li></ul><h2>Work Environment</h2><p>The role involves working 1/3 of the time at customer sites in the field, 1/3 in the factory with engineering, supplier quality, and project management teams, and 1/3 working independently on processes or reports. The position requires running a cross-functional team and quality council, including weekly meetings to discuss field data and problem-solving strategies. Travel across the US and Canada is required to support North American customers.</p><br>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a Quality Engineer with strong experience in manufacturing environments. This role supports organizational quality initiatives across customer programs and supplier engagements. The ideal candidate will lead quality assurance efforts, drive process improvements, and manage root cause and corrective action (RCCA) activities, including non-conformance investigations and implementation of effective solutions.</p><p><br></p><h2>Responsibilities</h2><ul><li>Ensure quality assurance for assigned programs from proposal through final delivery, ensuring compliance with customer expectations and internal cost and schedule goals.</li><li>Actively contribute to Integrated Product Teams (IPTs) and lead Failure Mode and Effects Analyses (FMEAs).</li><li>Coordinate and host external quality audits and participate in internal audit processes.</li><li>Serve as a liaison between the organization and suppliers/customers regarding quality requirements.</li><li>Develop, implement, and maintain quality systems and assurance programs.</li><li>Establish and monitor quality metrics for supplier performance.</li><li>Issue and manage Supplier Corrective Action Requests (SCARs) and internal Corrective and Preventative Actions (CAPAs).</li><li>Provide guidance on interpreting quality standards and regulatory requirements.</li><li>Analyze product and process reliability to recommend improvements.</li><li>Collaborate with engineering teams to ensure quality is embedded in product development and readiness.</li><li>Track and follow up on supplier audit action plans to ensure timely and accurate resolution.</li><li>Lead quality efforts in production, including materials, processes, assemblies, and returned product analysis (RMA).</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in interpreting engineering drawings and applying Geometric Dimensioning and Tolerancing (GD&amp;T).</li><li>Strong understanding of Statistical Process Control (SPC) and process capability analysis.</li><li>Familiarity with ISO 9001 and AS9100 quality management systems.</li><li>Experience in supplier quality assurance and continuous improvement methodologies.</li><li>Strong analytical and problem-solving abilities.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s or Master’s degree in a science or engineering discipline, preferably with a focus on electro-mechanical systems.</li><li>Experience with precision machining and assembly operations.</li><li>Understanding of Lean Manufacturing principles and ERP/MRP systems.</li><li>Proficiency in Microsoft Office Suite and familiarity with Microsoft Project.</li></ul><h2>Work Environment</h2><p>This position operates in a dynamic manufacturing environment, often requiring collaboration across various teams and external partners. The role involves occasional travel to supplier sites and customer locations to oversee quality audits and ensure compliance with established standards</p>

<h1 style="text-align: center;"><strong>Hiring for a Quality System Engineer (document control) in Putnam, CT!</strong></h1><p><br></p><h2>Job Description</h2><p>This is a full-time on-site role located in Putnam, CT, for a Quality System Engineer. The role involves managing day-to-day tasks related to quality management, auditing, quality assurance, and ensuring compliance with quality systems.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct internal documentation and internal auditing processes.</li><li>Perform risk assessments to drive the Corrective Preventative Action (CAPA) program.</li><li>Overhaul and enhance the CAPA process through effective root cause analysis.</li><li>Utilize ETQ quality systems for quality management.</li><li>Interact with customers and manage quality survey requests efficiently.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering expertise.</li><li>Proficiency in root cause analysis techniques such as 5 why&#39;s and fishbone method.</li><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in documentation quality assurance.</li><li>Experience in internal auditing.</li><li>Knowledge of ISO standards and quality systems.</li><li>Effective communication and interpersonal skills.</li><li>Bachelor&#39;s degree in Engineering, Quality Management, or related field.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Quality Assurance certification is a plus.</li><li>Experience with ETQ system.</li><li>Ability to prioritize tasks and maintain a positive attitude.</li></ul><h2>Work Environment</h2><p>The company specializes in custom polymer resin compounding, primarily catering to medical needs. The work involves creating materials that can be identified under scans, such as making catheters visible under x-rays. The quality team comprises 15 members, including technicians, Sr Quality Engineers, and a quality manager. </p>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Engineer will perform routine analysis on quality problems identified within the manufacturing process and resolve them through the application of acquired expertise guided by precedent. The role involves establishing and executing project quality plans, witness-points, and quality records for compliance with contract requirements, ensuring customer quality requirements and lessons learned are considered when analyzing proposed changes to improve processes. Additionally, the Quality Engineer will develop new solutions under guidance or in a team setting, collaborate with cross-functional teams to solve production quality problems, and deliver products as part of a team while performing analytical activities and maintaining quality metrics related to production quality.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform routine analysis on quality problems within the manufacturing process.</li><li>Resolve issues using acquired expertise guided by precedent.</li><li>Establish and execute project quality plans for compliance with contract requirements.</li><li>Ensure customer quality requirements and feedback are considered in process improvements.</li><li>Develop new solutions under guidance or in team settings.</li><li>Collaborate with cross-functional teams to solve production quality problems.</li><li>Deliver products as part of a team.</li><li>Perform analytical activities and maintain quality metrics related to production quality.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering knowledge.</li><li>Understanding of quality standards.</li><li>Experience with lean manufacturing techniques.</li><li>Bachelor&#39;s degree in Engineering (Mechanical, Industrial, Electrical).</li><li>Minimum of 2 years of experience in Manufacturing Quality.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with developing solutions in team settings.</li><li>Ability to collaborate with cross-functional teams.</li></ul><h2>Work Environment</h2><ul><li>The position is onsite five days a week.</li></ul>

<p><strong><em>Overview:</em></strong></p><p>We are currently seeking a Quality Engineer. </p><p><br></p><p><strong><em>Description:</em></strong></p><ul><li>Ensures efficient operation and proper functioning of the manufacturing processes in his/her control.</li><li>Specifies, purchases, coordinates, installs, samples, schedules, troubleshoots as well as maintains and improves all production processes, tools and equipment in the area assigned.</li><li>Works with customers and suppliers as needed to support APQP, Production, Delivery, Cost and or Quality issues.</li><li>Identifies and develops improvements to the processes in support of the company goals.</li><li>Understands and reports the daily status of production and quality (SPC, CpK, etc.) of all processes in this control and to initiate improvement as required.</li><li>Ensures a safe clean working environment.</li><li>Ensures 100% conformance to company Quality System and TS16949 in production operations.</li><li>Samples and qualifies new tools/products including PPAP preparation.</li><li>Samples and qualifies repaired existing tools.</li><li>Develops training materials and trains operators and supports employees.</li><li>Leads production teams, supervises hourly employees.</li><li>Ensures equipment is maintained.</li><li>Prioritizes tool changes in coordination with Manufacturing Manager.</li><li>Works with or leads APQP team and problem solving processes.</li></ul><p><strong><em>Qualifications:</em></strong></p><ul><li>Bachelor&#39;s Degree in Engineering.</li><li>2 years of experience within quality.</li><li>Exposure and experience with APQP and PPAP standards. </li><li>Computer Skills (MS Office)</li><li>Experience in sampling and qualifying new tools, products and processes.</li><li>Ability to read prints inch/metric.</li><li>Familiar with required measuring equipment.</li><li>Intermediate to advanced statistics knowledge.</li></ul>

<p><strong>Job Description</strong></p><p>The Quality Engineer is responsible for quality assurance activities to ensure production quality standards are met. This position coordinates with Operations, Customers, Suppliers, Sales, other Engineering personnel, Technicians, and Corporate support.</p><p><br></p><p>Essential Functions and Duties Include:</p><p>- Manage the PPAP process, including establishing requirements, gathering documentation, validating the process, and final approval.</p><p>- Develop Control Plans and FMEAs.</p><p>- Interpret data using CPK and CP.</p><p>- Apply knowledge of the IATF16949 technical standard.</p><p>- Establish process controls (Poke yokes, Check frequencies, etc.)</p><p>- Perform layered audits and internal process audits.</p><p>- Collaborate with Automotive OEMs in-person, on phone, and via email.</p><p>- Understand blueprint tolerances.</p><p>- Utilize measurement tools such as calipers, micrometers, and general hand gauges.</p><p>- Operate CMM, Faro arm, or other programmable measurement devices.</p><p>- Organize data to recommend actions to upper management.</p><p>- Implement formal problem-solving techniques (5P / 8D or equivalent).</p><p>- Supervise a team of 4+ associates across 3 shifts.</p><p><br></p><p><strong>Must Have</strong></p><p>- 3+ years quality engineering experience</p><p>- Experience in a fast paced manufacturing environment</p><p>- Some measurement tool usage (calipers, micrometers, and hand gauges)</p><p><br></p><p><strong>Nice to Have</strong></p><p>- Machining and/or aluminum products experience</p>

<p><strong><u>** Immediate Quality Engineering Opportunity!** </u></strong></p><p><br></p><p><strong><em>For immediate consideration, please apply directly to this job posting AND email habels @actalentservices.com with the following:</em></strong></p><p><strong>1) Word copy of resume</strong></p><p><strong>2) 2-3 professional references</strong></p><p><strong>3) 4-5 brief bullet points highlighting technical qualifications</strong></p><p><br></p><h2>Job Description</h2><p>As a Quality Engineer, your primary role will involve directly supporting the production floor by conducting complex troubleshooting through root cause analysis and investigations. You will apply engineering principles, statistical analysis, and scientific methods to implement corrective actions effectively.</p><p><br></p><h2>Responsibilities</h2><ul><li>Provide oversight and control to ensure all raw materials, component details, and finished products meet contractual quality requirements.</li><li>Manage supplier interactions and work with new product development programs to ensure supplier compliance with quality requirements.</li><li>Develop and communicate expectations for quality performance, continuous improvement, quality systems, process controls, and capabilities to suppliers.</li><li>Mentor and train supplier representatives in best practices concerning quality systems, process control methods, problem-solving, and statistical tools.</li><li>Develop supplier audit schedules, conduct supplier audits, and follow up on supplier corrective actions.</li><li>Maintain supplier programs, including ratings and metrics.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in quality engineering, root cause analysis, and corrective actions.</li><li>Expertise in statistical process control and lean methodologies.</li><li>Ability to apply scientific methods and engineering principles, including Fishbone Method, 5 WHYs, Failure Modes and Effects Analysis (FMEA), Fault Tree Analysis, and 8D Methodology.</li><li>Experience in metals and metal fabrication, including welding, machining, GD&amp;T, and working with materials like inconel, stainless steel, and aluminum.</li><li>Knowledge of quality assurance, audits, corrective action plans, and quality control standards such as AS9100 and ISO 9001.</li><li>Supplier quality management and first article inspection.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in Mechanical or Aerospace Engineering.</li><li>5-10+ years of experience in a manufacturing environment.</li><li>Certified Quality Engineer (CQE) is a bonus.</li><li>Experience in aerospace manufacturing, focusing on internal and supplier quality engineering.</li></ul><h2>Work Environment</h2><p>The work environment includes a large industrial production floor where you will be actively engaged with production workers. You will be aligned to space programs and production areas, focusing on metallic and composite air ducting systems for rockets. The role offers a hands-on experience with technical investigations, root cause analysis, and corrective actions implementation, not confined to paperwork. The company, a leader in ducting systems design and manufacturing, offers modest office space and a newer design center housing engineers.</p>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Engineer will be responsible for promoting and managing the quality system within the organization. This role involves conducting internal quality audits, participating in management review meetings, and ensuring compliance with relevant standards.</p><p><br></p><h2>Responsibilities</h2><ul><li>Promote and manage the quality system.</li><li>Conduct and coordinate internal quality audits and track audit actions for QMS.</li><li>Participate in management review meetings.</li><li>Report on processes such as QMS, final tests, and product audits.</li><li>Manage documents and records.</li><li>Participate in TTM projects as a team member.</li><li>Provide QG support.</li></ul><h2>Essential Skills</h2><ul><li>Technical degree in science, preferably a bachelor&#39;s in engineering or related field.</li><li>Minimum of five years of experience in a production environment.</li><li>Certified Quality Auditor (e.g., ASQ CQA, RAB Lead Assessor, BSI Quality Auditor).</li><li>Knowledge of ISO 9001.</li><li>Familiarity with quality tools like TTM, FMEA, Control Plan, SPC, ECR.</li><li>Proficiency in MS Office.</li></ul><h2><br></h2>

<h1><strong>Job Title: Quality Assurance Engineer</strong></h1><p>We are seeking a detail-oriented and experienced Quality Engineer to join our team. The ideal candidate will have a strong experience in automotive or manufacturing quality systems, with hands-on experience in PPAP and APQP processes. This role is critical in ensuring product quality from development through production, supporting continuous improvement and customer satisfaction.</p><h3><br></h3><h3>Key Responsibilities:</h3><ul><li>Lead and manage APQP activities for new product launches and engineering changes.</li><li>Prepare, review, and submit PPAP documentation in accordance with customer and industry requirements.</li><li>Collaborate with cross-functional teams including engineering, production, and suppliers to ensure quality standards are met.</li><li>Conduct FMEA, Control Plans, and Process Flow Diagrams as part of the APQP process.</li><li>Support internal and external audits, including IATF 16949 compliance.</li><li>Investigate and resolve quality issues using root cause analysis and corrective/preventive actions (8D, 5-Why, etc.).</li></ul>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><strong><em>For immediate consideration, please apply directly to this job posting AND email me at biacosta @actalentservices.com with the following:</em></strong></p><p><strong>1) Word copy of resume</strong></p><p><strong>2) 2-3 professional references</strong></p><p><strong>3) 4-5 brief bullet points highlighting technical qualifications</strong></p><p><br></p><h2>Job Description</h2><p>As a Quality Engineer, you will play a pivotal role in ensuring that our products meet customer requirements by reviewing engineering and manufacturing information on new and revised design documents, specifications, production, and tooling plans. You will develop and implement quality assurance techniques and prepare quality and inspection plans to ensure clear understanding of quality requirements. Analyzing and updating quality documents, and participating in the review and disposition of non-conforming materials, will be key aspects of this role.</p><p><br></p><h2>Responsibilities</h2><ul><li>Review engineering and manufacturing information to ensure products meet customer requirements.</li><li>Initiate and develop quality assurance techniques such as sampling plans and process controls.</li><li>Review customer contractual requirements to determine quality needs.</li><li>Prepare quality and inspection plans, procedures, and instructions.</li><li>Analyze and update quality documents within the quality system.</li><li>Participate in the review and disposition of non-conforming materials.</li><li>Collaborate with vendors, customers, and company personnel to resolve quality issues.</li><li>Initiate corrective action requests to address deficiencies in procedures, processes, or designs.</li><li>Lead and participate in continuous improvement activities to reduce scrap and rework.</li><li>Analyze inspection records and customer returns to improve product quality.</li><li>Provide guidance and quality-related training to employees.</li><li>Conduct internal quality system audits and product/process audits as per AS9100 and applicable standards.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s Degree in Engineering.</li><li>3-5+ years of experience in an Aerospace manufacturing environment.</li><li>3-5+ years of experience with First Article Inspection (FAI).</li><li>3-5+ years of experience with Corrective Action (CAPA).</li><li>Strong experience with AS9100/ISO9000 quality management systems.</li><li>Ability to read and interpret complex electrical and mechanical drawings.</li><li>Strong communication skills with vendors and customers.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience supervising quality lab and calibration technicians.</li></ul>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>Join a dynamic and growing manufacturing facility dedicated to producing high-quality aircraft and space engine components. Our team is seeking a Quality Engineer to ensure the accuracy and reliability of our production processes and play a critical role in process improvement and quality management.</p><br><h2>Responsibilities</h2><ul><li>Collaborate with engineering and manufacturing teams to develop corrective action plans for customer non-conformances.</li><li>Conduct process reviews on the production floor to ensure accurate and correct manufacturing practices.</li><li>Create and implement new process plans and quality plans for manufacturing new parts.</li><li>Develop work instructions and standards to maintain specifications.</li><li>Work extensively within the GE customer portal (Score) for submissions, corrective actions, and non-conformances.</li><li>Spend approximately 65% of time performing desk work in the quality office and 35% on the production/manufacturing floor.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in Engineering or Mathematics.</li><li>3+ years of experience as a Quality Engineer in a production/manufacturing environment.</li><li>Experience with process reviews and implementations.</li><li>Knowledge of AS9100 certification.</li><li>Familiarity with AS9145 elements (Aerospace APQP/PPAP process).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Previous experience working within the GE supplier system (Score).</li></ul><h2>Work Environment</h2><p>The work environment is characterized by a strong family culture and pride in the company&#39;s achievements. The temperature-controlled machine shop maintains a comfortable 73 degrees and is equipped with large machinery capable of producing substantial parts. The team is united in their mission and enjoys working in a company that supports the aerospace and space industry, collaborating with prominent names such as Rolls Royce, GE, and Blue Origin.</p><br>

<p>Are you passionate about ensuring top-notch quality in automotive parts? Join our dynamic team as a Quality Engineer, where you&#39;ll lead the charge in maintaining and improving the quality of supplier parts for new vehicle projects. Your role will be pivotal in guaranteeing that our parts meet international standards and exceed customer expectations.</p><p><br></p><p>Key Responsibilities:</p><ul><li>Quality Control Leadership: Spearhead quality inspection and improvement activities for supplier parts, ensuring they meet the highest standards.</li><li>Operational Excellence: Execute the Operation Plan to ensure part quality, including field claim analysis, supplier management, and part inspection.</li><li>Problem-Solving: Analyze the root causes of part issues, implement improvement activities, and lead quality meetings to drive continuous improvement.</li><li>Facility Management: Oversee quality facility and equipment management, manage investment costs, and establish supplementary investments.</li><li>Event Coordination: Prepare, consult, and coordinate external events to showcase our commitment to quality.</li><li>Project Participation: Play a crucial role in new vehicle projects by preparing for inspections, establishing quality plans, and responding to evaluations.</li></ul><p>Top Skills:</p><ul><li>Investigative Expertise: Proven experience in investigating mechanical and electrical parts, with a strong preference for automotive industry experience.</li><li>Industry Experience: At least 2 years of experience in quality engineering, mechanical engineering, or electrical engineering.</li><li>Technical Proficiency: Ability to understand drawings and specifications of electrical and mechanical systems.</li><li>Communication Skills: Excellent verbal and written communication skills, coupled with strong problem-solving abilities.</li><li>Quality Management: In-depth understanding of quality management systems.</li></ul><p>Additional Qualifications:</p><ul><li>Bachelor&#39;s degree in electrical engineering, mechanical engineering, or a related field.</li><li>Professional Experience: 2+ years of experience in quality engineering, mechanical engineering, or electrical engineering.</li><li>Automotive Expertise: Specific experience in the automotive industry is highly desirable.</li></ul><h1><br></h1>

<h1 style="text-align: center;"><strong>Hiring for a Quality Engineer in West Hartford!</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking skilled Quality Engineers to join our expanding quality department. With two immediate openings, we are looking for candidates who possess a strong machining <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> to contribute to our team.</p><p><br></p><h2>Responsibilities</h2><ul><li>Utilize ISO9001 and AS9100 standards in quality engineering practices.</li><li>Conduct root cause analysis to identify issues and implement effective solutions.</li><li>Perform supplier audits to ensure compliance and help build new supplier programs.</li><li>Engage in audits and regulatory compliance activities to uphold quality standards.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in quality engineering and quality assurance.</li><li>Experience with root cause analysis and supplier quality management.</li><li>Knowledge of ISO9001 and AS9100 quality management systems.</li><li>Machining skills and familiarity with CMM.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Familiarity with Windchill, Epicor, and Microsoft Office software.</li><li>Experience with quality management systems, particularly on Microsoft platforms.</li></ul><h2>Work Environment</h2><p>Join a historic company poised for growth with numerous upcoming contracts. Take advantage of new management and the opportunity to make a significant impact</p>

<h1><strong>Job Title: Process Chemical Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>Develops and utilizes key process indicators and statistical methods to determine process effectiveness, identify areas for improvement, best practices, and lead teams in driving continuous quality improvement. Leads, drives, and supports corrective and preventive actions, and effectiveness verification activities for product quality issues and customer complaints. Ensures that quality reporting and records related to incoming and in-process quality trends, returns analysis, complaint investigation, and corrective action activity are clearly documented and maintained.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and use key process indicators and statistical methods to assess process effectiveness.</li><li>Identify areas for improvement and implement best practices.</li><li>Lead teams in driving continuous quality improvement.</li><li>Support and drive corrective and preventive actions for product quality issues.</li><li>Verify the effectiveness of corrective and preventive actions.</li><li>Document and maintain quality reporting and records related to incoming and in-process quality trends.</li><li>Analyze returns and investigate complaints.</li><li>Ensure corrective action activities are clearly documented and maintained.</li></ul><h2>Essential Skills</h2><ul><li>B.S. degree in Chemical Engineering.</li><li>1 - 3 years of experience in a manufacturing environment with a focus on product quality.</li><li>Proficiency in Six Sigma methodologies.</li><li>Strong skills in root cause analysis.</li><li>Experience in process improvement.</li><li>Experience in chemical manufacturing.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of the Automotive Quality Standard IATF (or earlier versions) is a plus.</li></ul><h2>Work Environment</h2><p>The work environment includes developing a pilot plant to manufacture a new product, which will be a multimillion-dollar project. Operations include a diverse market such as consumer products, pharmaceuticals, and automotive industries, providing a dynamic and varied work experience.</p>

<h1><strong>Job Title: Quality Engineer - NPI</strong></h1><h2>Job Description</h2><p>As a Quality Engineer specializing in New Product Introduction (NPI), you will advocate and lead design for manufacture and assembly through technical leadership and direction in quality assurance, quality control, and preventative activities. You will support the development and introduction of new products, processes, and technologies with a focus on quality systems development, regulatory compliance, and process risk management, including pFMEA. Your role will involve developing and characterizing processes that are capable, scalable, and produce high yield, as well as supporting the design of robust inspection strategies including CQA&#39;s, CTQ&#39;s, and MSA&#39;s. You will provide quality engineering support for the execution of quality assurance activities during the design transfer phases of new product development.</p><p><br></p><h2>Responsibilities</h2><ul><li>Foster collaborative internal and external professional relationships across Design Divisions, Advanced Operations, and GQO functions associated with design transfer activities.</li><li>Communicate effectively with all internal customers, stakeholders, and project teams to deliver successful project transfers with the highest levels of quality that meet NPI project goals.</li><li>Mentor other groups and functions on areas of expertise, particularly focusing on design and process transfer.</li><li>Develop and implement methods and procedures for process control, process improvement, testing, and inspection to ensure products are free of flaws and function as designed.</li><li>Design and install sophisticated testing equipment and perform product testing and analysis to maintain quality levels and minimize defects and failure rates.</li><li>Analyze reports and defective products to determine trends and recommend corrective actions.</li><li>Collaborate with supplier representatives on quality problems, ensure effective corrective actions are implemented, and contribute to supplier quality improvement programs.</li><li>Proficient in risk management practices and tools, with high expertise in failure modes associated with production and production-related processes (PFMEA).</li><li>Support the Risk Management File through risk management principles, evaluating process risks, risk mitigation, and ensuring appropriate production and process controls are identified, qualified, and implemented throughout the product manufacturing lifecycle through robust pFMEA.</li><li>Ensure all Risk Management outputs comply with ISO14971.</li><li>Support the design team to complete CQA/CTQ identification and inputs to dFMEA to enable process risk identification, process characterization, process capability, and robust process control.</li><li>Develop and implement lean inspection strategies and inspection plans through state-of-the-art inspection methods and technologies, ensuring inspections are repeatable, efficient, and scalable.</li><li>Lead continuous improvements of inspection methods and sampling plans, focusing on human error risk elimination.</li><li>Lead First Article Inspection (FAI) strategies, both internally and externally, and approve First Article Inspections.</li><li>Optimize inspection costs through lean initiatives while maintaining the safety, integrity, and reliability of the product.</li><li>Develop Measurement System Analysis (MSA) strategy and approve executed MSAs.</li><li>Support the development, execution, and approval of validation strategies with the goal of highly capable processes that result in high yield and enable scalability.</li><li>Approve protocols and reports, including data analysis.</li><li>Influence processes towards validation versus manual verification, where possible.</li><li>Support sterilization validation activity, as required.</li><li>Apply appropriate statistical techniques to ensure the development of robust, predictive quality systems which are easily transferable and maintainable in a production environment.</li><li>Provide expertise for NC&#39;s &amp; CAPA&#39;s related to new products, acting as a subject matter expert and mentor in problem-solving and root-causing tools.</li><li>Support Design for Manufacture and Assembly (DFMA) through process design, inspection optimization, application of state-of-the-art technologies, and tooling &amp; fixture development.</li><li>Support ‘process benchmarking’ by providing quality experience as a process input.</li><li>Promote human factor error prevention and provide expertise in the science of human factor error risk identification and mitigation.</li><li>Lead the supplier qualification strategy and approve the supplier validations and Production Part Approval Process (PPAP).</li><li>Ensure Supplier’s Quality Systems can complete process characterization and develop highly capable processes that are scalable.</li><li>Provide Quality input to influence the proper selection of suppliers.</li><li>Support implementation of supplier certification.</li><li>Support Supplier Quality to establish Quality Agreements with sites and suppliers as part of NPI projects.</li><li>Represent quality assurance during the DTAP (Design Transfer Agreement Plan) process, ensuring product launches meet or exceed established metric targets.</li><li>Provide subject matter expertise in Design transfer processes and procedures, participating and interfacing in internal &amp; external audits with regulatory representatives.</li><li>Represent NPI Quality Assurance at Design reviews and ensure integrity of the process design through robust NPI quality deliverables.</li><li>Support device design into production specifications.</li><li>Lead the efficient and timely transfer of lessons learned knowledge to Quality engineering support and regional peers.</li><li>Provide expert quality process support post-launch per DTAP agreement.</li><li>Support the control of product through appropriate system containment to guard against product escape during pre-released builds.</li></ul><h2>Essential Skills</h2><ul><li>Experience in ISO standards, Design Transfer, Manufacturing, Risk Management, NPI, PFMEA, Validation, Quality engineering, Medical device, Design Control, and Product Transfer.</li><li>Bachelor of Science in Engineering or related subject.</li><li>3-5 years&#39; experience in a quality or technical discipline.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of CQA, CTQ, ISO14971, MSA, and PFMEA.</li><li>This role requires the use of judgment in applying professional expertise and working independently with minimal supervision.</li></ul><h2>Work Environment</h2><p>This position is onsite and offers standard benefits, including 2 weeks of PTO and 10 paid holidays. The work environment promotes collaboration and continuous improvement, focusing on maintaining high quality standards in a dynamic setting.</p>

Quality Engineer - NPI

<h1><strong>Job Title: Quality Engineer - NPI</strong></h1><p><strong><em>For immediate consideration, please apply directly to this job posting AND email me at biacosta @actalentservices.com with the following:</em></strong></p><p><strong>1) Word copy of resume</strong></p><p><strong>2) 2-3 professional references</strong></p><p><strong>3) 4-5 brief bullet points highlighting technical qualifications</strong></p><p><br></p><h2>Job Description</h2><p>As a Quality Engineer specializing in New Product Introduction (NPI), you will advocate and lead design for manufacture and assembly through technical leadership and direction in quality assurance, quality control, and preventative activities. You will support the development and introduction of new products, processes, and technologies with a focus on quality systems development, regulatory compliance, and process risk management, including pFMEA. Your role will involve developing and characterizing processes that are capable, scalable, and produce high yield, as well as supporting the design of robust inspection strategies including CQA&#39;s, CTQ&#39;s, and MSA&#39;s. You will provide quality engineering support for the execution of quality assurance activities during the design transfer phases of new product development.</p><p><br></p><h2>Responsibilities</h2><ul><li>Foster collaborative internal and external professional relationships across Design Divisions, Advanced Operations, and GQO functions associated with design transfer activities.</li><li>Communicate effectively with all internal customers, stakeholders, and project teams to deliver successful project transfers with the highest levels of quality that meet NPI project goals.</li><li>Mentor other groups and functions on areas of expertise, particularly focusing on design and process transfer.</li><li>Develop and implement methods and procedures for process control, process improvement, testing, and inspection to ensure products are free of flaws and function as designed.</li><li>Design and install sophisticated testing equipment and perform product testing and analysis to maintain quality levels and minimize defects and failure rates.</li><li>Analyze reports and defective products to determine trends and recommend corrective actions.</li><li>Collaborate with supplier representatives on quality problems, ensure effective corrective actions are implemented, and contribute to supplier quality improvement programs.</li><li>Proficient in risk management practices and tools, with high expertise in failure modes associated with production and production-related processes (PFMEA).</li><li>Support the Risk Management File through risk management principles, evaluating process risks, risk mitigation, and ensuring appropriate production and process controls are identified, qualified, and implemented throughout the product manufacturing lifecycle through robust pFMEA.</li><li>Ensure all Risk Management outputs comply with ISO14971.</li><li>Support the design team to complete CQA/CTQ identification and inputs to dFMEA to enable process risk identification, process characterization, process capability, and robust process control.</li><li>Develop and implement lean inspection strategies and inspection plans through state-of-the-art inspection methods and technologies, ensuring inspections are repeatable, efficient, and scalable.</li><li>Lead continuous improvements of inspection methods and sampling plans, focusing on human error risk elimination.</li><li>Lead First Article Inspection (FAI) strategies, both internally and externally, and approve First Article Inspections.</li><li>Optimize inspection costs through lean initiatives while maintaining the safety, integrity, and reliability of the product.</li><li>Develop Measurement System Analysis (MSA) strategy and approve executed MSAs.</li><li>Support the development, execution, and approval of validation strategies with the goal of highly capable processes that result in high yield and enable scalability.</li><li>Approve protocols and reports, including data analysis.</li><li>Influence processes towards validation versus manual verification, where possible.</li><li>Support sterilization validation activity, as required.</li><li>Apply appropriate statistical techniques to ensure the development of robust, predictive quality systems which are easily transferable and maintainable in a production environment.</li><li>Provide expertise for NC&#39;s &amp; CAPA&#39;s related to new products, acting as a subject matter expert and mentor in problem-solving and root-causing tools.</li><li>Support Design for Manufacture and Assembly (DFMA) through process design, inspection optimization, application of state-of-the-art technologies, and tooling &amp; fixture development.</li><li>Support ‘process benchmarking’ by providing quality experience as a process input.</li><li>Promote human factor error prevention and provide expertise in the science of human factor error risk identification and mitigation.</li><li>Lead the supplier qualification strategy and approve the supplier validations and Production Part Approval Process (PPAP).</li><li>Ensure Supplier’s Quality Systems can complete process characterization and develop highly capable processes that are scalable.</li><li>Provide Quality input to influence the proper selection of suppliers.</li><li>Support implementation of supplier certification.</li><li>Support Supplier Quality to establish Quality Agreements with sites and suppliers as part of NPI projects.</li><li>Represent quality assurance during the DTAP (Design Transfer Agreement Plan) process, ensuring product launches meet or exceed established metric targets.</li><li>Provide subject matter expertise in Design transfer processes and procedures, participating and interfacing in internal &amp; external audits with regulatory representatives.</li><li>Represent NPI Quality Assurance at Design reviews and ensure integrity of the process design through robust NPI quality deliverables.</li><li>Support device design into production specifications.</li><li>Lead the efficient and timely transfer of lessons learned knowledge to Quality engineering support and regional peers.</li><li>Provide expert quality process support post-launch per DTAP agreement.</li><li>Support the control of product through appropriate system containment to guard against product escape during pre-released builds.</li></ul><h2>Essential Skills</h2><ul><li>Experience in ISO standards, Design Transfer, Manufacturing, Risk Management, NPI, PFMEA, Validation, Quality engineering, Medical device, Design Control, and Product Transfer.</li><li>Bachelor of Science in Engineering or related subject.</li><li>3-5 years&#39; experience in a quality or technical discipline.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of CQA, CTQ, ISO14971, MSA, and PFMEA.</li><li>This role requires the use of judgment in applying professional expertise and working independently with minimal supervision.</li></ul><h2>Work Environment</h2><p>This position is onsite and offers standard benefits, including 2 weeks of PTO and 10 paid holidays. The work environment promotes collaboration and continuous improvement, focusing on maintaining high quality standards in a dynamic setting.</p>

<h1><strong>Job Title: Quality Engineer - NPI</strong></h1><p><strong><em>For immediate consideration, please apply directly to this job posting AND email me at habels @actalentservices.com with the following:</em></strong></p><p><strong>1) Word copy of resume</strong></p><p><strong>2) 2-3 professional references</strong></p><p><strong>3) 4-5 brief bullet points highlighting technical qualifications</strong></p><p><br></p><h2>Job Description</h2><p>As a Quality Engineer specializing in New Product Introduction (NPI), you will advocate and lead design for manufacture and assembly through technical leadership and direction in quality assurance, quality control, and preventative activities. You will support the development and introduction of new products, processes, and technologies with a focus on quality systems development, regulatory compliance, and process risk management, including pFMEA. Your role will involve developing and characterizing processes that are capable, scalable, and produce high yield, as well as supporting the design of robust inspection strategies including CQA&#39;s, CTQ&#39;s, and MSA&#39;s. You will provide quality engineering support for the execution of quality assurance activities during the design transfer phases of new product development.</p><p><br></p><h2>Responsibilities</h2><ul><li>Foster collaborative internal and external professional relationships across Design Divisions, Advanced Operations, and GQO functions associated with design transfer activities.</li><li>Communicate effectively with all internal customers, stakeholders, and project teams to deliver successful project transfers with the highest levels of quality that meet NPI project goals.</li><li>Mentor other groups and functions on areas of expertise, particularly focusing on design and process transfer.</li><li>Develop and implement methods and procedures for process control, process improvement, testing, and inspection to ensure products are free of flaws and function as designed.</li><li>Design and install sophisticated testing equipment and perform product testing and analysis to maintain quality levels and minimize defects and failure rates.</li><li>Analyze reports and defective products to determine trends and recommend corrective actions.</li><li>Collaborate with supplier representatives on quality problems, ensure effective corrective actions are implemented, and contribute to supplier quality improvement programs.</li><li>Proficient in risk management practices and tools, with high expertise in failure modes associated with production and production-related processes (PFMEA).</li><li>Support the Risk Management File through risk management principles, evaluating process risks, risk mitigation, and ensuring appropriate production and process controls are identified, qualified, and implemented throughout the product manufacturing lifecycle through robust pFMEA.</li><li>Ensure all Risk Management outputs comply with ISO14971.</li><li>Support the design team to complete CQA/CTQ identification and inputs to dFMEA to enable process risk identification, process characterization, process capability, and robust process control.</li><li>Develop and implement lean inspection strategies and inspection plans through state-of-the-art inspection methods and technologies, ensuring inspections are repeatable, efficient, and scalable.</li><li>Lead continuous improvements of inspection methods and sampling plans, focusing on human error risk elimination.</li><li>Lead First Article Inspection (FAI) strategies, both internally and externally, and approve First Article Inspections.</li><li>Optimize inspection costs through lean initiatives while maintaining the safety, integrity, and reliability of the product.</li><li>Develop Measurement System Analysis (MSA) strategy and approve executed MSAs.</li><li>Support the development, execution, and approval of validation strategies with the goal of highly capable processes that result in high yield and enable scalability.</li><li>Approve protocols and reports, including data analysis.</li><li>Influence processes towards validation versus manual verification, where possible.</li><li>Support sterilization validation activity, as required.</li><li>Apply appropriate statistical techniques to ensure the development of robust, predictive quality systems which are easily transferable and maintainable in a production environment.</li><li>Provide expertise for NC&#39;s &amp; CAPA&#39;s related to new products, acting as a subject matter expert and mentor in problem-solving and root-causing tools.</li><li>Support Design for Manufacture and Assembly (DFMA) through process design, inspection optimization, application of state-of-the-art technologies, and tooling &amp; fixture development.</li><li>Support ‘process benchmarking’ by providing quality experience as a process input.</li><li>Promote human factor error prevention and provide expertise in the science of human factor error risk identification and mitigation.</li><li>Lead the supplier qualification strategy and approve the supplier validations and Production Part Approval Process (PPAP).</li><li>Ensure Supplier’s Quality Systems can complete process characterization and develop highly capable processes that are scalable.</li><li>Provide Quality input to influence the proper selection of suppliers.</li><li>Support implementation of supplier certification.</li><li>Support Supplier Quality to establish Quality Agreements with sites and suppliers as part of NPI projects.</li><li>Represent quality assurance during the DTAP (Design Transfer Agreement Plan) process, ensuring product launches meet or exceed established metric targets.</li><li>Provide subject matter expertise in Design transfer processes and procedures, participating and interfacing in internal &amp; external audits with regulatory representatives.</li><li>Represent NPI Quality Assurance at Design reviews and ensure integrity of the process design through robust NPI quality deliverables.</li><li>Support device design into production specifications.</li><li>Lead the efficient and timely transfer of lessons learned knowledge to Quality engineering support and regional peers.</li><li>Provide expert quality process support post-launch per DTAP agreement.</li><li>Support the control of product through appropriate system containment to guard against product escape during pre-released builds.</li></ul><h2>Essential Skills</h2><ul><li>Experience in ISO standards, Design Transfer, Manufacturing, Risk Management, NPI, PFMEA, Validation, Quality engineering, Medical device, Design Control, and Product Transfer.</li><li>Bachelor of Science in Engineering or related subject.</li><li>3-5 years&#39; experience in a quality or technical discipline.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of CQA, CTQ, ISO14971, MSA, and PFMEA.</li><li>This role requires the use of judgment in applying professional expertise and working independently with minimal supervision.</li></ul><h2>Work Environment</h2><p>This position is onsite and offers standard benefits, including 2 weeks of PTO and 10 paid holidays. The work environment promotes collaboration and continuous improvement, focusing on maintaining high quality standards in a dynamic setting.</p>

<h1><strong>Job Title: Quality Engineer </strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a diligent and detail-oriented Quality Engineer  with expertise in Trackwise to ensure compliance with CAPA processes and procedures. The ideal candidate will be responsible for reviewing and approving non-conformance (NC) and corrective and preventive actions (CAPAs) with a focus on completeness, accuracy, effectiveness, and timeliness. This role involves facilitating and guiding teams through all stages of the NC/CAPA process and maintaining rigorous documentation within the eCAPA system. Additionally, the candidate will play a key role in continuous improvement initiatives and engage in cross-site and corporate projects.</p><p><br></p><h2>Responsibilities</h2><ul><li>Ensure compliance with CAPA processes and procedures.</li><li>Review and approve NC and CAPAs, ensuring completeness of actions and records, accuracy, effectiveness, and timeliness.</li><li>Liaise with relevant functional groups and guide teams through all stages of the NC/CAPA process.</li><li>Ensure timely maintenance of a live record with all relevant evidence attached in the eCAPA system.</li><li>Build expertise in facilitating NC and CAPA teams and promote the use of problem-solving techniques (e.g., human error reduction, 4-D, 5 Why&#39;s, fishbone diagrams, process mapping).</li><li>Serve as a highly proficient eCAPA super-user.</li><li>Execute the NC/CAPA review board forums.</li><li>Monitor site NC/CAPA KPIs, including reporting requirements, and provide detailed updates for quality and business review forums.</li><li>Ensure compliance with global requirements and metrics.</li><li>Identify continuous improvement and collaboration opportunities.</li><li>Engage in cross-site and corporate project teams in the NC/CAPA area of expertise.</li><li>Coordinate preparation, participation, and follow-up for internal, corporate, and third-party audit activities.</li></ul><h2>Essential Skills</h2><ul><li>Experience in interacting with regulatory agencies (FDA, MoH, TUV, etc.).</li><li>Ability to gain knowledge and understanding of U.S. and International medical device regulations.</li><li>Supporting Quality Systems (audits, management review, quality planning, etc.).</li><li>Strong communication and influencing skills.</li><li>Ability to manage multiple tasks simultaneously.</li><li>Strong interpersonal skills.</li><li>Problem-solving skills.</li><li>Analytical thinking skills.</li><li>Ability to work independently.</li><li>Comfort working in a compliance-risk situation.</li><li>Computer literacy, including Microsoft Word, Excel, and PowerPoint.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in Engineering, Quality Management, or a related field.</li><li>Minimum of 1-2 years of experience in quality engineering within the medical device industry.</li><li>Proficiency in Trackwise software.</li><li>In-depth understanding of NCR, CAPA processes, and regulatory requirements for medical devices.</li><li>ASQ Certified Quality Engineer (CQE) or equivalent preferred.</li></ul><h2>Work Environment</h2><p>You will enjoy 2 weeks of PTO and 10 paid holidays. The role involves a collaborative work environment where you will interact with various functional groups and participate in cross-site and corporate projects. The work may involve compliance-risk situations, requiring meticulous attention to detail and adherence to regulatory standards. The position also offers opportunities for continuous improvement and professional development.</p>

Quality Engineer I Trackwise)

<h1 style="font-weight: 700;">Job Title: Quality Engineer II</h1><br><h2>Job Description</h2><p>As a Quality Engineer II, you will play a vital role in ensuring the quality performance of products and processes. You will work closely with operations and various business functions, collaborating with cross-functional teams to address quality issues and improve manufacturing processes. Your expertise will drive the approval of NC/CAPA, and proficiency in problem-solving and root-cause analysis.</p><br><h2>Responsibilities</h2><ul><li>Collaborate with operations and business functions to ensure product and process quality.</li><li>Engage with customers, sales, marketing, and field personnel to address top quality issues.</li><li>Approve NC/CAPA and enhance proficiency in problem-solving and root-cause activities.</li><li>Participate in the development and improvement of manufacturing processes for existing products.</li><li>Review change management activities and maintain KPIs for monitoring process and product quality.</li><li>Perform analysis, interpret trends, and take necessary actions based on KPI findings.</li><li>Manage execution and analysis of complaints and product field actions.</li><li>Advocate for Human Factor practices and familiarize with Human Factor science.</li><li>Develop understanding of risk management practices and concepts.</li><li>Optimize inspection methods and sampling, and develop proficiency in statistical methods.</li><li>Engage in internal audits and participate in external audit preparation.</li><li>Assist in the development and review of process and equipment validation/qualification.</li><li>Execute quality activities during manufacturing transfers to other plants/facilities.</li><li>Initiate, contain, and support ship and product holds for potential product escapes.</li></ul><h2>Essential Skills</h2><ul><li>Proven experience in quality engineering and quality assurance.</li><li>Familiarity with supplier, production, and design quality.</li><li>Experience with quality audits and ISO standards.</li><li>Knowledge of US and International Medical Device Regulations.</li><li>Understanding of GDP and GMP practices.</li><li>Proficient in Quality Concepts such as Risk Management, CAPA, Audits, and Statistics.</li><li>Strong communication, project management, and influencing skills.</li><li>Ability to manage multiple tasks simultaneously.</li><li>Capability to represent the Quality function within project teams.</li><li>Strong interpersonal, written, oral communication, and negotiation skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Previous industry experience is desired.</li><li>Experience interacting with regulatory agencies like FDA, MoH, TUV is preferred.</li><li>Strong critical thinking and problem-solving skills.</li><li>Ability to work independently and as part of cross-functional teams.</li><li>Computer literacy is essential.</li></ul><h2>Work Environment</h2><p>This position is based onsite in Irvine, CA. The role offers a comprehensive benefits package including 2 weeks of PTO and 10 paid holidays.</p><br>

Quality Engineer II

<h1><strong>Job Title: Quality Engineer Manager </strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a skilled Quality Engineer with proven leadership capabilities to oversee and enhance our quality assurance systems. The ideal candidate will be responsible for ensuring compliance with medical device regulations, improving manufacturing processes, and driving continuous quality improvements within our dynamic and growing company.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop, implement, and maintain quality assurance policies, procedures, and systems to ensure product quality and compliance.</li><li>Lead and mentor the quality assurance team, including quality engineers and quality control technicians.</li><li>Ensure all products and processes comply with relevant medical device regulations and standards, including ISO and FDA 21 CFR Part 11 and Part 820 requirements.</li><li>Prepare and manage documentation in support of regulatory submissions, audits, and inspections.</li><li>Oversee the monitoring of injection molding processes to ensure consistent product quality.</li><li>Identify and implement process improvements to enhance product quality, reduce waste, and improve manufacturing efficiency.</li><li>Analyze data on product quality and process performance to identify trends and areas for improvement.</li><li>Prepare and present reports on quality metrics and performance to <span style="color: rgb(8, 7, 7); background-color: none;">senior</span> personnel.</li><li>Lead root cause analysis and corrective action activities for non-conforming products.</li><li>Collaborate with cross-functional teams, including production, engineering, and R&amp;D, to implement effective corrective and preventive actions.</li><li>Manage supplier quality performance, including conducting supplier audits and assessments.</li><li>Work with suppliers to resolve quality issues and ensure the supply of high-quality materials.</li><li>Serve as the primary point of contact for customer quality concerns and complaints.</li><li>Support customer audits and visits by providing necessary documentation and information.</li><li>Drive continuous improvement initiatives aimed at enhancing product quality, reducing costs, and improving efficiency.</li><li>Lead and participate in cross-functional quality improvement teams.</li><li>Develop and conduct training programs for quality assurance personnel and promote a culture of quality awareness and continuous improvement within the organization.</li><li>Conduct internal audits to ensure compliance with quality management systems and regulatory requirements.</li><li>Prepare for and support external audits by regulatory bodies and customers.</li></ul><h2>Essential Skills</h2><ul><li>Minimum of 7-10 years of experience in a quality role within the medical device manufacturing industry.</li><li>Extensive experience in plastic injection molding.</li><li>Previous management experience required.</li><li>5+ years experience with FDA 21 CFR Part 11 and Part 820.</li><li>5+ years experience with ISO 9001.</li><li>Strong leadership and team management skills.</li><li>Excellent analytical and problem-solving skills.</li><li>Proficiency in statistical analysis and quality management software.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in engineering, preferably in Mechanical, Industrial, or Plastics Engineering. A master’s degree is a plus.</li><li>Certifications such as Certified Quality Manager (CQM), Certified Quality Engineer (CQE), and/or Certified Quality Auditor (CQA) from ASQ are highly desirable.</li><li>In-depth understanding of quality assurance principles and methodologies.</li><li>Extensive knowledge of injection molding processes and equipment.</li><li>Familiarity with medical device regulations and standards.</li><li>Practical experience and knowledge of metrology and GD&amp;T techniques.</li><li>Effective communication and interpersonal skills.</li></ul><h2>Work Environment</h2><p>This role is set in a fast-paced, deadline-driven manufacturing floor and office environment, requiring strong attention to detail and adaptability to shifting priorities.</p>

Quality Engineer Manager

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>We are seeking a skilled Quality Engineer with proven leadership capabilities to oversee and enhance our quality assurance systems. The ideal candidate will be responsible for ensuring compliance with medical device regulations, improving manufacturing processes, and driving continuous quality improvements within our dynamic and growing company.</p><br><h2>Responsibilities</h2><ul><li>Develop, implement, and maintain quality assurance policies, procedures, and systems to ensure product quality and compliance.</li><li>Lead and mentor the quality assurance team, including quality engineers and quality control technicians.</li><li>Ensure all products and processes comply with relevant medical device regulations and standards, including ISO and FDA 21 CFR Part 11 and Part 820 requirements.</li><li>Prepare and manage documentation in support of regulatory submissions, audits, and inspections.</li><li>Oversee the monitoring of injection molding processes to ensure consistent product quality.</li><li>Identify and implement process improvements to enhance product quality, reduce waste, and improve manufacturing efficiency.</li><li>Analyze data on product quality and process performance to identify trends and areas for improvement.</li><li>Prepare and present reports on quality metrics and performance to <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span> personnel.</li><li>Lead root cause analysis and corrective action activities for non-conforming products.</li><li>Collaborate with cross-functional teams, including production, engineering, and R&amp;D, to implement effective corrective and preventive actions.</li><li>Manage supplier quality performance, including conducting supplier audits and assessments.</li><li>Work with suppliers to resolve quality issues and ensure the supply of high-quality materials.</li><li>Serve as the primary point of contact for customer quality concerns and complaints.</li><li>Support customer audits and visits by providing necessary documentation and information.</li><li>Drive continuous improvement initiatives aimed at enhancing product quality, reducing costs, and improving efficiency.</li><li>Lead and participate in cross-functional quality improvement teams.</li><li>Develop and conduct training programs for quality assurance personnel and promote a culture of quality awareness and continuous improvement within the organization.</li><li>Conduct internal audits to ensure compliance with quality management systems and regulatory requirements.</li><li>Prepare for and support external audits by regulatory bodies and customers.</li></ul><h2>Essential Skills</h2><ul><li>Minimum of 7-10 years of experience in a quality role within the medical device manufacturing industry.</li><li>Extensive experience in plastic injection molding.</li><li>Previous management experience required.</li><li>5+ years experience with FDA 21 CFR Part 11 and Part 820.</li><li>5+ years experience with ISO 9001.</li><li>Strong leadership and team management skills.</li><li>Excellent analytical and problem-solving skills.</li><li>Proficiency in statistical analysis and quality management software.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in engineering, preferably in Mechanical, Industrial, or Plastics Engineering. A master’s degree is a plus.</li><li>Certifications such as Certified Quality Manager (CQM), Certified Quality Engineer (CQE), and/or Certified Quality Auditor (CQA) from ASQ are highly desirable.</li><li>In-depth understanding of quality assurance principles and methodologies.</li><li>Extensive knowledge of injection molding processes and equipment.</li><li>Familiarity with medical device regulations and standards.</li><li>Practical experience and knowledge of metrology and GD&amp;T techniques.</li><li>Effective communication and interpersonal skills.</li></ul><h2>Work Environment</h2><p>This role is set in a fast-paced, deadline-driven manufacturing floor and office environment, requiring strong attention to detail and adaptability to shifting priorities.</p><br>

<h1><strong>Job Description: Quality Engineer</strong></h1><p>We are seeking a dedicated Quality Engineer who is committed to adhering to safety regulations and contributing to a safe work environment. The ideal candidate will possess a keen attention to detail, ensuring that quality standards are consistently met. They should be proficient in analytical and problem-solving skills, with the ability to identify issues and develop proactive solutions that enhance efficiency. Familiarity with data analysis and visualization tools such as Power BI, Tableau, Excel, SQL, and Python is crucial, along with strong organizational skills to manage multiple tasks efficiently.</p><p><br></p><h2>Responsibilities</h2><ul><li>Analyze data using statistical tools to identify trends and generate actionable insights for quality and efficiency improvements.</li><li>Lead and coordinate corrective and preventive actions in response to customer complaints and non-conformances, managing the investigation and resolution process from start to finish.</li><li>Utilize expertise in root cause analysis (RCA) to identify underlying issues, applying 8D methodology to structure problem-solving processes and develop effective solutions that prevent recurrence.</li><li>Oversee the non-conformance process by identifying, documenting, and tracking quality issues, collaborating closely with production teams to address deviations from product specifications.</li><li>Support the development, implementation, and continuous improvement of the Quality Management System (QMS) in accordance with ISO 9001 and AS 9100 standards, leading internal audits and ensuring compliance with relevant industry standards and regulations.</li><li>Collaborate with engineering and production teams to identify and implement process improvements, leveraging Lean and Six Sigma principles to reduce waste, improve quality, and streamline production processes.</li><li>Provide guidance and training to production teams on quality standards, inspection procedures, and best practices, promoting a culture of continuous improvement.</li><li>Perform other duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Strong understanding of Quality Management Systems (QMS) and familiarity with ISO 9001 and AS 9100 standards.</li><li>Experience in root cause analysis and problem-solving methodologies such as 8D or FMEA.</li><li>Excellent communication and interpersonal skills for effective collaboration with internal teams, external suppliers, and customers.</li><li>Ability to produce clear, concise documentation and reports.</li><li>Bachelor&#39;s Degree in Quality Assurance, Engineering, Manufacturing, or a related field.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of Six Sigma principles and methodologies.</li><li>Experience with PPAP, internal and external audits.</li><li>Expertise in quality control, management, and assurance in automotive and aerospace industries.</li></ul>

Quality Engineering

<h1><strong>Job Title: Quality Engineering Technician</strong></h1><p><br></p><h2>Job Description</h2><p>This role requires a dedicated and proactive individual to join the engineering team as a Quality Engineering Technician on the 3rd shift. </p><p>The technician will serve as the main liaison between the Quality Engineers and the Machinists, ensuring the smooth operation and quality of products. </p><p>This technical position demands strong problem-solving abilities, as it involves conducting capability studies, identifying non-conformances, and implementing corrective actions.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct capability studies to assess production processes.</li><li>Identify non-conformances and develop corrective actions to ensure product specifications are met.</li><li>Read and interpret PFMEAs, inspection plans, work instructions, and control plans.</li><li>Perform tasks in strict compliance with manufacturing standards (SOPs) and regulatory requirements (i.e., GMPs).</li><li>Collaborate on calibration processes.</li><li>Demonstrate ownership and accountability to the production schedule, ensuring product quality.</li><li>Maintain documentation for auditing purposes.</li><li>Check and update quality control policies.</li><li>Monitor different stages of production to prevent product defects.</li></ul><h2>Essential Skills</h2><ul><li>Experience conducting capability studies.</li><li>Ability to identify non-conformances.</li><li>Proficiency in quality documentation, including reading work instructions, inspection plans, and PFMEAs.</li><li>Proven problem-solving skills.</li><li>Calibration experience.</li><li>Associates degree in Engineering or Quality certification.</li></ul><h2>Work Environment</h2><p>The position is onsite, requiring a 40-hour work week on the 3rd shift. </p><p>The technician will collaborate with all departments, primarily serving as the liaison between engineering and machinists. </p><p>The role involves spending significant time on the production floor, with approximately 30% dedicated to documentation tasks. </p><p>Training will initially occur on the 1st shift. The work environment offers autonomy in managing workloads and opportunities for internal promotion. </p><p>Employees receive 10 days of PTO, 6 paid holidays, and access to Udemy after 6 months.</p>

Quality Engineering Technician

<h1><strong>Job Title: Quality Engineering Technician</strong></h1><p><br></p><h2>Job Description</h2><p>The primary objective of this role is to ensure quality in manufacturing and supply chain in support of the development and production of the driver, delivering the benefits of self-driving technology safely, quickly, and broadly. A successful candidate understands quality processes, possesses strong attention to detail, has a quality-focused mindset, and can contribute to cross-functional teams to identify and eliminate quality problems, issues, and risks.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead and support inspection and test plan creation in coordination with engineering.</li><li>Provide guidance related to part inspection and test procedures.</li><li>Perform inspections (first article, incoming, in-process, outgoing) according to inspection plans and procedures to record, analyze data, document, and report results.</li><li>Perform tests (qualification, incoming, in-process, end-of-line) according to test plans and procedures to record, analyze data, document, and report results.</li><li>Conduct physical inspections using various gauges, tools, and inspection equipment.</li><li>Perform dimensional and gauge studies (MSA, R&amp;R) in coordination with engineering.</li><li>Carry out cable and harness assembly testing and troubleshooting.</li><li>Perform soldering and wire splicing inspections.</li><li>Assemble electromechanical modules.</li><li>Execute inventory physical and electronic transactions as needed.</li><li>Operate inspection and test fixtures or equipment, with the ability to train others as required.</li><li>Assist in training manufacturing teams and technicians on in-process inspections and/or tests.</li><li>Support activities related to non-conforming product(s) and returned material authorization activities (Material Review Board).</li><li>Participate in layered audit and manufacturing process audit activities.</li><li>Actively engage in continuous improvement activities.</li><li>Follow and support company safety requirements, policies, procedures, and work instructions.</li><li>Adhere to written, verbal, and visual instructions.</li><li>Perform other duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance expertise in automotive manufacturing and electro-mechanical assembly operations.</li><li>3+ years of experience in quality automotive manufacturing, robotics, or equivalent field.</li><li>Proficiency in debugging complex electronic assemblies and manufacturing cable assemblies.</li><li>Experience with CNC mills, lathes, and other machine shop tools.</li><li>Understanding of electrical and mechanical drawings.</li><li>Proficient in using various gauges, measuring devices, and equipment.</li><li>Experience with Linux operating systems.</li><li>Experience with Google Sheets, Docs, Slides, and Gmail.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>An Associate Degree, Technician Certificate, or equivalent in engineering/photonics/lasers/electro-optics.</li><li>IPC 610 and IPC 620 certifications.</li><li>Attention to detail and careful handling of precision components and equipment.</li></ul><h2>Work Environment</h2><p>This is an on-site position with meals provided.</p>

<h1><strong>Quality Coordinator </strong></h1><h2>Job Description</h2><p>We are seeking a dedicated Quality Coordinator to support the inventory, setup, and documentation of new equipment acquired. The role involves supporting O2 and CO2 cylinder change outs in both GMP and Non-GMP labs, conducting walkdowns, and performing gauge and equipment checks with required documentation. The Quality Coordinator will also handle manual documentation, technical documentation, and quality checks, as well as oversee on-site contractors and help track timelines.</p><p><br></p><h2>Responsibilities</h2><ul><li>Support inventory, setup, and documentation of new equipment</li><li>Assist with O2 and CO2 cylinder change outs in GMP &amp; Non-GMP labs, ensuring proper documentation in GMP logbooks</li><li>Conduct walkdowns and gauge and equipment checks with necessary documentation</li><li>Perform manual documentation, technical documentation, and quality checks</li><li>Oversee and check on-site contractors and help track timelines</li><li>Support cleaning and upkeep functions in main areas</li></ul><h2>Essential Skills</h2><ul><li>Quality check</li><li>Visual inspection</li><li>Documentation review</li><li>Quality assurance</li><li>Inspection</li><li>Facility management</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>HS Diploma (Associates or Bachelors preferred)</li><li>Prior experience in quality coordination</li><li>Experience with documentation, SOP review, and GMP protocols</li><li>Mechanically inclined</li></ul><p><br></p>

Quality Facility Coordinator

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