quality engineer

Crane Aerospace & Electronics

<div><p><b>Crane Aerospace and Electronics </b>has an exciting opportunity for a <b>Quality Engineer </b>at our <b>Burbank, CA </b>location.<br>
</p><p></p><p><b>About Crane:<br>
</b></p><p></p><p><b>Crane Aerospace &amp; Electronics </b>supplies critical systems and components to the aerospace and defense markets. You&rsquo;ll find Crane Aerospace &amp; Electronics in some of the toughest environments: from engines to landing gear; from satellites to medical implants and from missiles to unmanned aerial systems (UAS).
</p><p></p><p>Every 1.2 seconds, product built at our Crane Aerospace &amp; Electronics Burbank facility is stopping aircraft &ndash; delivering passengers and military personnel safely to their destination. Home to our Landing &amp; Cabin Systems team, Crane A&amp;E&rsquo;s brake control systems and premium cabin actuation solutions are flying on tens of thousands of aircraft throughout the world. You&rsquo;ll join a business with a long track record of engineering excellence, set in the wonderful town of Burbank filled with great community atmosphere, schools, weather and no shortage of entertainment. Start the next chapter of your career with Crane Aerospace &amp; Electronics!
</p><p></p><p><b>Job Summary:
</b></p><p>The Quality Engineer works under supervision and uses established procedures to control and monitor quality, ensuring products are consistent with industry standards, government regulations, and customer requirements.
</p><p></p><p><b>Essential Functions:
</b></p><ul><li>Collaborate cross-functionally with Engineering, Operations, Suppliers, and Customers to ensure quality standards are met and maintained.
</li><li>Collect, analyze, and interpret production data to evaluate product quality, identify trends, and drive continuous improvement.
</li><li>Lead root cause analysis for quality issues and recommend corrective and preventive actions to mitigate risks effectively.
</li><li>Halt production processes if critical product defects are identified to prevent nonconforming material from reaching customers.
</li><li>Monitor and maintain quality control systems to ensure their effectiveness, efficiency, and compliance with industry standards.
</li><li>Train and mentor team members in quality control methodologies, statistical analysis, and analytical procedures.
</li><li>Generate detailed reports on nonconformance of products or processes, root cause analyses, and quality trends for management and stakeholders.
</li><li>Review and interpret statistical studies, regulatory standards, and emerging trends in quality control to ensure compliance and continuous improvement.
</li><li>Identify critical control points in the Value Stream and establish appropriate sampling procedures to monitor and improve quality.
</li><li>Lead and drive the qualification of product and process changes, ensuring adherence to the highest quality standards and customer requirements.
</li><li>Support and participate in audits conducted by Defense, Aerospace, and Customer Auditors, ensuring compliance with industry and customer requirements.
</li><li>Provide technical support for failure analysis, reliability testing, and corrective action implementation as required.
</li><li>Review and approve quality-related document changes, including Engineering Change Orders (ECOs), Manufacturing Change Orders (MCOs), and deviations.
</li><li>Perform process capability analysis and ongoing data reviews to ensure processes remain stable and capable.
</li><li>Collaborate with cross-functional teams to develop and maintain Control Plans, PFMEAs, and Process Flow Diagrams (PFDs) to mitigate risks and improve processes.
</li><li>Any other task assigned by supervisor or management.
</li></ul><p></p><p><b>Eligibility Requirement: </b>This position may require access to Controlled Data or Information. Where the position requires such access only US Persons will be considered. As a US Department of Defense contractor, we are bound by International Traffic in Arms Regulations (ITAR).
</p><p></p><p><b>Minimum Qualifications </b><b>:
</b></p><ul><li><i>Experience </i>:
<ul><li><i>Level I </i><i>: </i>0-2 years of Quality Engineering experience
</li><li><i>Level II </i><i>: </i>2+ years of experience as a Quality Engineer in an Aerospace environment or similar manufacturing setting
</li></ul></li></ul><ul><li><i>Knowledge </i>: Familiar with SPC, AS9145, standard concepts, practices, and procedures within the field; Knows and applies the fundamental concepts, practices and procedures of assigned product or program
</li><li><i>Skills/Abilities </i>: Demonstrated ability to rely on limited experience and judgment to plan and accomplish goals; Excellent written and verbal communication skills; Ability to establish and maintain effective working relationships with internal staff and outside professionals; Proficient in the use of Word, Excel, Outlook, and PowerPoint
</li><li><i>Education/Certification </i>: BA or BS degree in Quality, Electrical, Mechanical Engineering, or related field
</li><li><i>Eligibility Requirement </i>: FAA sensitive position &ndash; may be subject to a Government security investigation to verify eligibility for access to classified information
</li></ul><p></p><p><b>Preferred Qualifications </b><b>:
</b></p><ul><li>Proficiency in Lean Principles and Implementation Tools
</li><li>Educational background in Structured Problem Solving, 5S, Mistake-Proofing and process capability tools
</li><li>Familiarity with Minitab
</li><li>ASQC Quality Engineer Certification
</li></ul><p></p><p><b>Working Conditions </b><b>:
</b></p><ul><li>Standard office environment
</li><li>Work requires substantial visual concentration on detail
</li><li>Working conditions are normal for a manufacturing environment
</li><li>Manufacturing operations may require the use of safety equipment to include but not limited to: eye safety glasses, gowning, masks, hearing protectors, heel/wrist straps and any other required PPE
</li><li>May be exposed to unusual environmental conditions such as loud noises, cold temperatures, confined spaces, dust or fumes
</li></ul><p></p><p>Standing: 10% *percentage is approximate and may vary depending on work task
</p><p>Sitting: 90% *percentage is approximate and may vary depending on work task
</p><p>Lifting (in pounds): up to 25 pounds
</p><p>Pushing (in pounds): up to 25 pounds
</p><p>Mental/Visual: use of computer, microscope
</p><p>Workspace (line, cube, etc): cubicle/desk/work cell
</p><p></p><p><b>Top Benefits:
</b></p><p></p><p>As a team member at Crane Aerospace and Electronics, you&rsquo;ll enjoy:
</p><ul><li><b>Benefits: </b>Health care, dental, vision, life and disability insurance starting the first day of the month
</li><li><b>Time Off: </b>15 days of paid time off that start accruing your first day at Crane and 12 paid holidays per year.
</li><li><b>401k Retirement Plan: </b>401k plan with company match
</li><li><b>Education Reimbursement: </b>eligible after 6 months of employment<br>
</li></ul><p></p><p>You can see a list of our benefits at https://www.craneae.com/company/careers or visit our website at www.CraneAE.com for more information on our company and great opportunities.<br>
</p><p></p><p>We are committed to operational excellence and world class processes. We employ Lean manufacturing techniques to optimize manufacturing efficiency and accuracy on all product lines. Our products are known for their technical strength, proven reliability and overall value.<br>
</p><p></p><p>In our efforts to maintain a safe and drug-free workplace, Crane Aerospace &amp; Electronics requires that candidates complete a satisfactory background check. FAA sensitive positions require employees to participate in a random drug test pool.
</p><p>#LI-SP1 #CAE
</p><p></p><p><i>Salary range:
</i></p><p><i>Level I: $80,801.00 - $98,800.00
</i></p><p><i>Level II: </i>$95,800.00 - 112,600.00
</p><p>Several factors contribute to actual salary, including experience in a similar role or performing comparable job responsibilities, skills, training, and other qualifications. Some roles may be eligible for participation in performance-based bonus programs.
</p><p></p><p><i>This description has been designed to indicate the general nature and level of work being performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.
</i></p><p></p><p><i>Crane Company. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, color, religion, gender, sexual orientation, general identity, national origin, disability or veteran status.</i></p></div>

Quality Engineer-2

Confidential

<div>
 <p>
  <strong>
   About the Role
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Quality Engineer will be responsible for implementing and monitoring quality standards across tunneling project activities.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Ensures compliance with project specifications, QA/QC procedures, and regulatory requirements.
  </li>
  <li>
   Conducts inspections, tests, and documentation to verify work quality.
  </li>
  <li>
   Coordinates with contractors and site teams to resolve non‑conformities and ensure continuous improvement.
  </li>
  <li>
   Supports audits, prepares quality reports, and ensures all tunneling works meet project and safety standards.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s Degree
  </li>
  <li>
   + 5 years Tunneling Experience Required
  </li>
 </ul>
 <p>
 </p>
</div>


Quality Engineer

Colson Group

<div><p>Colson Group USA is an operating unit of Colson Group the largest manufacturer of caster and wheel products in the world. The brands of Colson Group USA have been technological leaders in caster innovation for over 350 combined years. This drive has led to some of the most trusted, advanced, and highest-quality mobility solutions available in the world today. Colson Group's unique and proprietary global footprint provides available services and capabilities unmatched by any other manufacturer.
</p><p>The Quality Engineer supports efforts and plans to coordinate the quality control program designed to ensure continuous production consistent with established standards for Colson Group worldwide. A proven hands-on and metrics-driven approach to driving results in a multi-cultural environment is a critical success factor.
</p><p><b>Essential Job Functions
 </b></p><p>Support One Colson quality and continuous improvement strategies, programs, and procedures.
</p><ul><li>Drive Statistical Process Control (SPC) methods for analyzing data.
</li><li>Maintain the CPAR quality reporting process and related follow.
</li><li>Implement continuous improvement activities identified by Director of Quality as related to product quality.
</li><li>Maintains quality control objectives, and coordinates objectives with production procedures to maximize quality, reliability and minimize costs.
</li><li>Conduct training activities related to quality and reliability.
</li><li>Investigates customer complaints regarding quality and makes appropriate adjustments.
</li><li>Collaborates with Engineering, Operations, and ISCs on daily basis for project planning and resolution of complaint cases.
</li><li>Willingness to travel up to 25% - customers and internal.
</li><li>Ensure that quality-related product risks are adequately controlled in accordance with internal requirements and customer expectations.
</li><li>Acting as main point of contact for product quality escalations internally and externally.
</li><li>Follow directives for maintaining and improving departmental operational performance to meet the requirements of regulatory authorities, company Standard Operating Procedures (SOPs), external / internal customers, with respect to quality, service, lead time and cost.
</li><li>Development of departmental SOPs (writing, revising, and approving), ensuring regulatory compliance in conjunction with being &lsquo;fit for purpose&rsquo; operationally and commercially.
</li><li>Perform activities in accordance with Colson company SOPs and Health and Safety policies.
</li><li>Support internal audit programs in place, perform and report as scheduled.
</li><li>Support Part Submission Warrants and customer respective forms for Advance Product Quality Planning.
</li><li>Supporting all validation activities, including validation strategy and approval of protocols and reports.
</li><li>Providing support and awareness of new quality legislation and testing that impacts the business.
</li>Performs other related duties and projects as assigned.<br>
<li>
</li></ul><p></p><div><div><div><div><p>&middot;</p></div></div></div></div></div><p></p>
<br><div><p><b>Knowledge
</b></p><ul><li>Associate degree or quality engineer certification required.
</li><li>Bachelor&rsquo;s degree preferred.
</li><li>Understanding of Lean Manufacturing, APQP, PPAP and 8D Processes.
</li><li>Knowledge of Control Plans, DOE, FMEA&rsquo;s, Root Cause Analysis, Capability Analysis, Probability, etc.
</li>Quality Certification- 6 Sigma, and fully familiar with the ISO9001 Standards ideally Lead Auditor training for QMS Assessment.<br>
<li>
</li></ul><p></p><p><b>Experience
</b></p><ul><li>Five years experience of progressive quality control responsibilities within an organization.
</li><li>Five years previous Quality Engineer experience in a manufacturing environment.
</li>Four years experience with ISO 9001/TS-16949 compliance.<br>
<li>
</li></ul><p></p><p><b>Skills
</b></p><ul><li>Ability to work in a highly matrixed environment.
</li><li>Broad knowledge of theory and statistical principles as well as statistical process control.
</li><li>Excellent communication skills-written and verbal.
</li><li>Ability to manage multiple priorities to completion.
</li><li>Ability to work in a highly collaborative team environment.
</li><li>Ability to effectively communicate and work with customers and other members of the organization.
</li><li>Ability to work with both front-line manufacturing and corporate employees.
</li><li>Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
</li><li>Strong Understanding of ISO 9001/TS-16949 Compliance
</li><li>Strong analytical and problem-solving ability Strong Feasibility, Factory Acceptance Testing and Validation is a plus.</li></ul></div>

Lam Research

<div><div><div><div>Requisition ID</div><div><b>
197385</b></div></div><div><div>
Date posted</div><div><b>
04/02/2026</b></div></div><div><div>
Work Location Model</div><div><b>
On-site Flex</b></div></div><div><div>
Work Location</div><div><b>
Tualatin-OR</b></div></div><div><div>
Work Country</div><div><b>
United States</b></div></div></div><div><div><div><div><div><h2 class="jobSectionHeader"><b>
The group you&rsquo;ll be a part of</b></h2>
</div><div><p>
The Global Operations Group brings information systems, facilities, supply chain, logistics, and high-volume manufacturing together to drive the engine of our global business operations. We help Lam deliver industry-leading solutions with speed and efficiency, while actively supporting the resilient and profitable growth of Lam's business.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>The impact you&rsquo;ll make</b></h2>
</div><div><p>
As a Quality Engineer at Lam, you will make an impact by ensuring manufacturing processes and products meet established quality standards. You will design, implement, and maintain quality assurance practices within the quality management system (QMS). In this role, you will design methods for inspecting, testing, and evaluating the accuracy of production processes and finished products. By analyzing production data and reports, you will identify trends and collaborate cross‑functionally to resolve technical, quality, and production challenges. Your expertise will help drive excellence in product design and manufacturing, supporting Lam&rsquo;s commitment to delivering high‑quality, reliable products.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
What you&rsquo;ll do</b></h2>
</div><div><ul><li>Performs analysis of production data to identify trends and recommend updates or changes to quality defect detection, reporting, and improvement programs.</li><li>
Supports disposition of supplier quality issues in manufacturing by applying defined criteria and prioritizing issues for RCCA using a combination of recurrence, part value, and impact to operations.</li><li>
Conducts preliminary analysis of quality escapes to assign further investigation to the appropriate investigation function. Utilizes 8D methodology to drive manufacturing‑owned escapes through root cause analysis and CAPA (Corrective Action, Preventive Action) planning and execution.
</li><li>Ensures systematic solutions are fully deployed and presents RCCA (root‑cause corrective action) findings to stakeholders.</li><li>
Monitors the quality of investigations and RCCA (Root Cause/Corrective Action) conducted by stakeholders (Product Groups and Supply Chain), ensuring a high probability that issues will not recur in Manufacturing.</li><li>
Supports Global Quality and GOPS quality projects, as well as Management System Assessments (audits).</li><li>
Performs GEMBAs on the manufacturing cleanroom floor and interviews technicians to investigate quality escapes and identify improvement opportunities, gathering information on potential causes.</li><li>
Reviews build instructions, performs risk assessments, and provides feedback to MFE (Manufacturing Engineering) on manufacturability of deposition products. At times, updates build process instructions for manufacturing inspections and quality checks.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Who we&rsquo;re looking for</b></h2>
</div><div><ul><li>Bachelor&rsquo;s degree in Mechanical, Chemical, or Industrial Engineering, with 5 years of relevant experience; or 3 years of experience with a Master&rsquo;s degree; or a PhD with no prior experience; or equivalent work experience.</li><li>
Excellent analytical and problem‑solving skills.</li><li>
Strong communication, interpersonal, and negotiation skills.</li><li>
Comfortable working in a fast‑paced, dynamic, and changing environment.</li><li>
Demonstrated ability to communicate effectively and work collaboratively with technicians building and testing products in a cleanroom environment.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Our commitment</b></h2>
</div><div><p>
We believe it is important for every person to feel valued, included, and empowered to achieve their full potential. By bringing unique individuals and viewpoints together, we achieve extraordinary results.</p><p></p><p><br>
Lam Research (&quot;Lam&quot; or the &quot;Company&quot;) is an equal opportunity employer. Lam is committed to and reaffirms support of equal opportunity in employment and non-discrimination in employment policies, practices and procedures on the basis of race, religious creed, color, national origin, ancestry, physical disability, mental disability, medical condition, genetic information, marital status, sex (including pregnancy, childbirth and related medical conditions), gender, gender identity, gender expression, age, sexual orientation, or military and veteran status or any other category protected by applicable federal, state, or local laws. It is the Company's intention to comply with all applicable laws and regulations. Company policy prohibits unlawful discrimination against applicants or employees.</p><p></p><p><i><br>
Lam offers a variety of work location models based on the needs of each role. Our hybrid roles combine the benefits of on-site collaboration with colleagues and the flexibility to work remotely and fall into two categories &ndash; On-site Flex and Virtual Flex. &lsquo;On-site Flex&rsquo; you&rsquo;ll work 3+ days per week on-site at a Lam or customer/supplier location, with the opportunity to work remotely for the balance of the week. &lsquo;Virtual Flex&rsquo; you&rsquo;ll work 1-2 days per week on-site at a Lam or customer/supplier location, and remotely the rest of the time.</i></p><p></p><p><br>
#LI-YS1</p></div></div></div><p><b>
Our Perks and Benefits</b></p><p><br>
At Lam, our people make amazing things possible. That&rsquo;s why we invest in you throughout the phases of your life with a comprehensive set of outstanding benefits.</p></div></div></div>

Quality Engineer 3

General Atomics

<p></p><div><div><div><div><p>General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems.<br>
<br>
We have an exciting opportunity for an experienced Quality Engineer to join our Flight Operations Quality Assurance Team. This position reports to a manager, or senior level manager, and is responsible for execution of the Quality Management System for emerging and legacy engine manufacturing and Depot lines. The position develops, modifies, documents, and directs the implementation and evaluation of quality assurance programs and systems on one or more mid-size to large projects. Provides expertise and guidance in interpreting quality standards and government regulations. Collaborates with engineering and manufacturing to ensure quality standards are in place. Works on moderately complex and diverse problems where analysis of situations or data requires in-depth evaluation of various factors.<br>
<br>
<b>DUTIES AND RESPONSIBILITIES:</b></p><ul><li>
Identifies and recommends design or manufacturing changes and enhancements.</li><li>
Determines technical objectives for quality assurance as well as approaches to completing projects.</li><li>
Creates or recommends design, dimensional, or manufacturing process changes to improve products and reduce costs.</li><li>
Devises and implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment. Participates in functional testing and/or inspection of equipment and systems.</li><li>
Audits quality systems for deficiency identification and correction. Implements solutions to complex problems occurring internally and at vendor facilities.</li><li>
May prepare statistical analysis reports, specifications, and other technical documents.</li><li>
Interprets and adapts quality standards and government regulations.</li><li>
Acts as company contact with suppliers, customers, and regulatory personnel to resolve quality issues.</li><li>
Delivers technical presentations.</li><li>
Provides project direction to other staff members.</li><li>
Responsible for observing all laws, regulations, and other applicable obligations wherever, and whenever, business is conducted on behalf of the Company.</li><li>
Expected to work in a safe manner in accordance with established operating procedures and practices.</li><li>
Additional Functions: Other duties as assigned or required.</li></ul><p>
We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply.</p></div><br>
</div><div><p><b>Job Qualifications</b></p>
<div><ul><li>Typically requires a bachelor's or master's degree in engineering or related discipline and two or more years of related experience. May substitute equivalent experience in lieu of education.</li><li>
Must be able to apply a detailed understanding of inspection methods and have strong knowledge of computer operations and applications.</li><li>
Must have a strong knowledge of concepts, techniques, and methods in a particular field of specialization.</li><li>
Must have the analytical ability required to develop creative solutions to complex quality issues and the skills required to present those solutions to internal and external contacts.</li><li>
Must be detail-oriented to accurately prepare statistical reports and technical documents in support of company objectives.</li><li>
Must be a proactive, highly functional individual that works well within a diverse atmosphere and have strong leadership skills to direct staff members and ensure project costs and schedules are maintained, while representing the organization on technical quality assurance issues.</li><li>
Able to deliver effective technical presentations and work extended hours as required.</li><li>
Ability to obtain and maintain a DoD Security Clearance required.</li></ul></div>
</div><div><p><b>Job Category</b></p>
<div>Quality</div>
</div><div><p><b>Experience Level</b></p>
<div>Entry-Level (0-2 years)
</div></div><div><p><b>Workstyle</b></p>
<div>Onsite</div>
</div><div><p><b>Full-Time/Part-Time</b></p>
<div>Full-Time Salary
</div></div><div><p><b>Pay Range Low</b></p>
<div>68,770</div>
</div><div><p><b>Pay Range High</b></p>
<div>116,193</div>
</div><div><p><b>Travel Percentage Required</b></p>
<div>0% - 25%
</div></div><div><p><b>Relocation Assistance Provided?</b></p>
<div>No</div>
</div><div><p><b>US Citizenship Required?</b></p>
<div>Yes</div>
</div><div><p><b>Clearance Required?</b></p>
<div>Desired</div>
</div><div><p><b>Clearance Level</b></p>
<div>Secret</div></div></div></div><div></div>

Argon Medical Devices

<div>Company Overview::
<div>
Argon Medical Devices is a global manufacturer of specialty medical products. Argon offers a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology and Oncology. Argon&rsquo;s brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. Our values describe what we believe in and how we operate. These values are our moral compass which guide our decisions and define the deeply held beliefs and principles of our organizational culture. Argon Medical is a family of individuals united by a mission and culture which continue to grow stronger every day.</div><div></div><div><b><br>
ARGON MEDICAL DEVICES IS NOT LEVERAGING SEARCH FIRMS / AGENCIES!!!</b></div><div><b>
This position is not eligible for visa sponsorship</b></div>
Position Overview::
<div>
The Quality Engineer, Post Market Experience plays a key role in data-driven post-market surveillance, analyzing complaint, vigilance, and field performance data using tools such as Power BI to identify trends, detect potential safety signals, and support risk management activities. This role assists in evaluating regulatory requirements for product impact and supports the development and maintenance of post-market surveillance documentation and procedures.</div><br>
<div></div>
What you will do::
<ul><li>Analyze complaint, adverse event, and medical device reporting data to identify trends and communicate findings to internal stakeholders.</li><li>
Support preparation and maintenance of global post-market surveillance documentation including:</li><li><ul><li>
Post Market Surveillance Plans (PMSP)</li><li>
Periodic Safety Update Reports (PSUR)</li><li>
Post Market Surveillance Reports (PMSR)</li><li>
Summary of Safety and Clinical Performance (SSCP)</li></ul></li><li>
Assist in the development and implementation of quality system processes supporting EU MDR post-market surveillance requirements.</li><li>
Support preparation of technical reports related to product performance, safety, and complaint trending.</li><li>
Assist in monitoring post-market data including complaints, adverse events, CAPA trends, and field actions to identify potential safety signals.</li><li>
Support data analysis and visualization activities related to post-market surveillance using tools such as Power BI or similar reporting platforms.</li><li>
Participate in cross-functional product review and risk review meetings to provide post-market performance insights.</li><li>
Assist with regulatory submissions, audits, and inspections related to post-market surveillance activities.</li><li>
Support new product development activities related to post-market surveillance planning and risk management.</li></ul>
Skills for Success::
<ul><li>Bachelor&rsquo;s degree in Engineering, Biomedical Engineering, Life Sciences, or related technical discipline</li><li>
2&ndash;5 years of experience in Quality Engineering, Post Market Surveillance, or medical device quality/regulatory roles</li><li>
Experience working within a regulated healthcare environment (ISO 13485 and/or 21 CFR Part 820)</li><li>
Hands-on experience with data analysis, including use of tools such as Power BI, Excel, or similar platforms</li><li>
Experience analyzing complaint or post-market data</li><li>
Self-directed with ability to complete tasks in accordance with deadlines</li><li>
Critical thinking and problem solving</li><li>
Strong written and verbal communication skills</li><li>
Strong data analysis and data visualization skills (Power BI or similar tools)</li><li>
Data analysis, interpretation, and presentation</li><li>
Attention to detail and regulatory documentation accuracy</li></ul></div>

Ryan Companies US, Inc.

<div><p><b>Job Description:</b></p><p></p><p>
The Quality Engineer ensures that all phases of all mission-critical projects performed by the company or its subcontractors are carried out with the desired level of quality from inception through turnover.</p><p></p><p><b>
Some things you can expect to do:</b></p><ul><li><p>
Capture and share lessons learned with suppliers and project teams.</p></li><li><p>
Support commissioning, punch list, and turnover activities.</p></li><li><p>
Recommend effective implementation of corrective and preventive actions for project non-conformances and quality issues.</p></li><li><p>
Attend factory witness tests for Owner Furnished Contractor Installed (OFCI) and CFCI equipment and systems.</p></li><li><p>
Conduct Root Cause Analysis to identify, resolve, and implement solutions to quality issues.</p></li><li><p>
Provide Quality Control by reviewing Construction Documents for errors and omissions.</p></li><li><p>
Generate startup reports to document equipment readiness.</p></li><li><p>
Manage mechanical, electrical, and control systems testing and submit all related documentation, including testing and calibration reports and turnover packages.</p></li><li><p>
Conduct routine job site audits and site walks to ensure quality installations, compliance with codes, and adherence to safety requirements.</p></li><li><p>
Attend required safety training and comply with company and site safety regulations and requirements.</p></li></ul><p></p><p><b><br>
Eligibility:</b></p><p>
Position requires verification of employment to work in the U.S.</p><p></p><p><b>
Benefits:</b></p><ul><li><p>
Competitive Salary</p></li><li><p>
Medical, Dental and Vision Benefits</p></li><li><p>
Retirement and Savings Benefits</p></li><li><p>
Flexible Spending and Health Savings Accounts</p></li><li><p>
Life Insurance</p></li><li><p>
Short-Term and Long-Term Disability</p></li><li><p>
Educational Assistance</p></li><li><p>
Paid Time Off (PTO)</p></li><li><p>
Employee Assistance and Wellness Programs</p></li><li><p>
Parenting Benefits</p></li><li><p>
Employee Discount Programs</p></li><li><p>
Pet insurance</p></li><li><p>
Ryan Foundation &ndash; charitable matching funds</p></li><li><p>
Paid Time for Volunteer Events</p></li></ul><p></p><p><i><br>
Disclaimer: Eligibility may vary based on factors such as role, hours worked, employment status, length of service, location, and other considerations. Detailed information will be shared with eligible candidates during the hiring process, and the official terms and conditions will be outlined in each individual offer document.</i></p><p></p><p>
Ryan Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.</p><p></p><p><b>
Non-Solicitation Notice to Recruitment Agencies:</b></p><p>
Ryan Companies kindly requests that recruitment agencies and third-party recruiters do not submit unsolicited resumes or candidate information to any Ryan Companies employee or office. Ryan Companies will not be responsible for any fees or expenses associated with unsolicited submissions. If recruitment services are required, we will reach out directly to agencies on our approved vendor list. We appreciate your understanding and cooperation.</p><p><b>
Candidate Requirements:</b></p><ul><li><p>
Bachelor's degree in Engineering or related discipline required.</p></li><li><p>
Three years of related experience required.</p></li><li><p>
Previous experience in Construction Project Management focusing on mechanical, electrical, and plumbing engineering (MEP) systems is required.</p></li><li><p>
Attention to detail with the ability to handle a variety of project tasks.</p></li><li><p>
High level of professionalism, honesty and integrity.</p></li><li><p>
Ability to travel as needed for project success.</p></li><li><p>
Knowledge of complex data center MEP Systems preferred.</p></li></ul></div>

Search 10000+ Quality engineer jobs near you this April. New roles added regularly across leading industries. Apply today.

10000 quality engineer jobs Near Me

Quality Engineer-2

Quality Engineer

Quality Engineer

Quality Engineer 3

Quality Engineer

Quality Engineer

Quality Engineer