quality improvement engineer

SIG SAUER, Inc.

<div><p><b>Quality Engineer I</b></p>
<p><b>
SIG SAUER, Inc</b>. is a leading provider and manufacturer of firearms, electro-optics, ammunition, airguns, suppressors, remote controlled weapons stations, and training. For over 250 years SIG SAUER, Inc. has evolved, and thrived, by blending American ingenuity, German engineering, and Swiss precision. Today, SIG SAUER is synonymous with industry-leading quality and innovation which has made it the brand of choice amongst the U.S. Military, the global defense community, law enforcement, competitive shooters, hunters, and responsible citizens. Additionally, SIG SAUER is the premier provider of elite firearms instruction and tactical training at the SIG SAUER Academy. Headquartered in Newington, New Hampshire, SIG SAUER employs people across various U.S. locations, and global facilities across multiple regions. SIG SAUER is certified a <b>Great Place to Work&trade;.</b> For more information about the company and product line visit: <b>www.sigsauer.com</b><b>.</b></p>
<p><b>
Position Summary: </b>The Quality Engineer I will ensure the overall quality of manufactured products, tests processes, create documentation, devise quality tests, and define the criteria a test result should meet. This individual will also monitor quality standards and track performance trends to identify areas of needed improvement.</p>
<p>
FLSA: Exempt</p>
<p><b>
Job Duties and Responsibilities:</b></p>
<ul>
<li>Collect and review inspection data to ensure component integrity and investigate and resolve discrepancies found during part inspection.</li>
<li>Update control plans for correct gauges and order of operation.</li>
<li>Collect data for runoff and gauge study.</li>
<li>Generate and drive to completion CARs as assigned by Supervisor.</li>
<li>Able to review and disposition non-compliant material of minor issue complexity.</li>
<li>Assess issue culpability with assistance from senior staff as needed.</li>
<li>Identify features for inspection and correctly assign dimensional values and tolerances specified in print to a given feature.</li>
<li>Develop and document ISO-compliant standards under direction of Senior Engineers.</li>
<li>Expected to contribute to primary areas of inspection for which training has been provided.</li>
<li>Engage in Continuous Improvement projects and tasks.</li>
<li>Participate in and sustain 5S Standards.</li>
<li>Follow all required Safety and ISO procedures.</li>
<li>Miscellaneous duties as assigned.</li>
</ul>
<p><b>Education/Experience &amp; Skills:</b></p>
<ul>
<li>Bachelor&rsquo;s degree in Engineering or equivalent combination of education and experience, and 0-3 years of experience required.</li>
<li>Proficient in blueprint reading.</li>
<li>Understand the ISO process.</li>
<li>Basic understanding of the requirements of ATF compliance. Full understanding of the critical role ATF compliance plays in the continued health of the business.</li>
<li>Understand and work fluently with GD&amp;T symbology assigned per ASME Y14.5.</li>
<li>Must be able to clearly, concisely, and accurately convey ideas and information to others, both verbally and in written form.</li>
<li>Complete tasks as assigned in a timely manner.</li>
<li>Communicate effectively to supervision verbally and in written format regarding problems and corrective action.</li>
</ul>
<p><b>Working Conditions:</b></p>
<ul>
<li>Prolonged periods of sitting at a desk and working at a computer using a keyboard and mouse performing repetitive tasks.</li>
<li>Ability to open file cabinets, reach with hands and arms, bend, and twist, lift and move files.</li>
<li>Ability to lift up to 25 pounds.</li>
<li>Must wear required Personal Protective Equipment (PPE) where required.</li>
<li>Must comply with all work exposure EH&amp;S training requirements and adhere to SIG SAUER Inc. Security Mandates.</li>
</ul>
<p>Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by law.</p></div>

Quality Engineer I

Knauf MEASA

<div><p><b>QUALITY MANAGEMENT &amp; CONTINUOUS IMPROVEMENT ENGINEER - AHIBOZ<br>
</b></p><p><br>
<b>Knauf stands for opportunity</b>. We know that opportunity looks different to each person, and we are proud that we see opportunity in everyone. This exciting role within the Procurement Department could be the perfect next opportunity for you to build a unique career, in a values-led culture with a clear purpose of making tomorrow a home for all of us.</p><p>
We are a global manufacturer of construction materials and within our Group, our <b>43,500 team members</b> in <b>98 countries</b> across <b>300 sites</b> provide a huge opportunity for anyone with ambition and energy. We value everyone's contribution equally and we ask that you bring your whole self to work, to enrich the business further, as together we achieve more in a safe and inclusive environment.</p><p>
Knauf T&uuml;rkiye is proud to be part of the Knauf Group. We have a 30-year heritage in high quality, market-leading gypsum building products manufacturing and have big plans for the future. Our global reach in 98 countries continues to grow and we are looking for passionate, ambitious people to help us achieve our goals. We are all led by the same core values and believe in the powerful potential of large companies to have a positive impact on the world. <b>We are now looking for another team mate to join us in Ankara Ahiboz Plant as Quality Management &amp; Continuous Improvement Engineer.</b></p><p></p><p><b>
Can you say &lsquo;yes&rsquo;?</b></p><p>
Do you treat your colleagues with respect?</p><p>
Do you always have the customer in mind?</p><p>
Do you act with future generations in mind?</p><p>
Do you like to seek out opportunities to grow and develop?</p><p>
Do you have a proven track record of delivering results?</p><p></p><p><b>
What you&rsquo;ll be doing:</b></p><ul><li><p>
Plan and coordinate the effectiveness and continuity of the ISO 9001 quality management system implemented in our company; ensure the creation, implementation, and maintenance of the necessary processes for the systems</p></li><li><p>
Prepare and periodically execute plans for internal and external (customer and supplier) audits</p></li><li><p>
Conduct audits to ensure compliance with established rules and procedures within factory workflows</p></li><li><p>
Ensure successful implementation of improvement projects and measurement of their results</p></li><li><p>
Provide internal trainings on continuous improvement methodologies such as corrective actions and suggestion systems; promote and expand their use</p></li><li><p>
Evaluate process change requests from departments and ensure required actions are taken by coordinating all parties through the system</p></li><li><p>
Keep processes continuously up to date; maintain regular communication with process owners, be informed of necessary changes in a timely manner, and ensure process adjustments are made accordingly</p></li><li><p>
Ensure on-site implementation of structured flows (5S, A3, Kaizen, Visual Management, SQCDPE, Standard Work)</p></li><li><p>
Lead the planning, coordination, and delivery of quality system trainings; ensure effectiveness through evaluations; support other departments with training</p></li><li><p>
Coordinate the preparation of all quality system documents and ensure continuity by identifying and managing revision needs</p></li><li><p>
Assess risks and opportunities, report corrective actions, and follow up on their effectiveness</p></li><li><p>
Coordinate and track correspondence to respond to customer requests (documents, certificates, declarations, questionnaires, etc.)</p></li><li><p>
Represent the company during audits and support factory processes (system audits, product audits, product surveillance audits, etc.)</p></li><li><p>
Ensure the preparation of technical files related to CE certifications and carry out the relevant markings</p></li><li><p>
Monitor and maintain the currency of TSE (Turkish Standards Institution) standards and internal company standards</p></li><li><p>
Monitor departmental targets tracked by the units; take necessary measures and report when deviations occur</p></li><li><p>
Lead continuous improvement initiatives by conducting necessary analyses and reporting</p></li><li><p>
Actively participate in the customer complaint process managed by the customer service unit and lead root cause analysis efforts by bringing together different departments</p></li></ul><p><b><br>
What we&rsquo;d love for you to have:</b></p><p>
We are interested in you as a person: your attitude, behaviors and values. As long as you have the willingness to learn anything you need for the role that you don't already have, we'd love to speak to you. If you have experience in the following areas &ndash; this is an added advantage:</p><ul><li><p>
Bachelor&rsquo;s degree in Chemical Engineering or Industrial Engineering (preferred)</p></li><li><p>
Received basic training in ISO 9001 Quality Management System and ISO 45001, as well as internal auditor and documentation training; experienced in establishing integrated management systems</p></li><li><p>
At least 2 years of experience serving as Management Representative for ISO 9001 quality management systems</p></li><li><p>
Fluent in English (speaking, writing, and comprehension)</p></li><li><p>
Proficient in MS Office applications</p></li><li><p>
Preferably an active user of the QDMS program</p></li><li><p>
Preferably experienced with JMP/Minitab and ability to work with SPC methodology.</p></li><li><p>
Preferably holds a Lean Six Sigma Green Belt certification</p></li><li><p>
Knowledgeable about problem-solving techniques</p></li><li><p>
Team-oriented with strong leadership, representation, and communication skills</p></li><li><p>
For male candidates: completion of mandatory military service</p></li></ul><p></p><p><b>
What happens next?</b></p><p>
We appreciate that your time is precious and applying for a new job can be a lengthy process - so we have committed to replying to your application as soon as possible.</p></div>

Quality Management & Continuous Improvement Engineer - Ahiboz

Marotta Controls

<div><div><div><div><div><div><div><div><div><div><div><div><div><div>Elevate your career at Marotta Controls, a New Jersey Top Workplace three years running! Dedicated to innovation, quality and excellence, we deliver cutting edge control systems for the Aerospace &amp; Defense industry. At Marotta, we value bold thinking and teamwork, and we empower our employees to push boundaries while delivering top-tier solutions to our customers. Our team fosters a fun, collaborative culture where creativity and technical excellence thrive! Your next big opportunity starts here. Be part of a company where your work supports a mission that makes a difference&mdash;apply today!</div><br>
<div>
</div></div></div></div></div></div></div></div></div></div></div></div></div><div></div><div><b>Quality Engineer II - Space Systems</b>
<div></div><div><b>Overview:</b></div>
<div>The Quality Engineer supports program quality initiatives and monitors quality performance for both the Supply Chain and for internal development and production to ensure effective process control are employed. This role leads root cause analysis and corrective action activities, supports continuous improvement initiatives with ability to present results to customer and senior management. QE assists in supporting company goals for program Quality and Delivery targets.</div>
<div></div><div><b>Essential or Primary / Key Responsibilities</b><b>:</b></div>
<ul><li>Develop procedures from various industry and aerospace specifications</li>
<li>Investigate, assess, and resolve production problems in a team environment</li>
<li>Represent Quality for Programs / Customers</li>
<li>Review Drawings- flowdown, best practices</li>
<li>Review and approve component FAI&rsquo;s</li>
<li>Coordinate completion of customer FAI&rsquo;s</li>
<li>Support in-process product reviews</li>
<li>Acceptance Data Package Preparation/ Review</li>
<li>Support Audits &ndash; Customer / Internal</li>
<li>Support customer inquiries, including requests for warranty support, lead corrective action activities</li>
<li>Work internally and externally to develop Risk Analysis and Mitigation plans</li>
<li>Promote the use of Quality tools, SPC, PFMEA, and MSA to reduce variability</li>
<li>Actively participate in cost reduction programs/initiatives related to scrap, rework and repair activities.</li>
<li>Provide guidance and training to internal personnel and suppliers to effectively execute Corrective Action Requests (inclusive of SCARs), Quality System requirements, Quality Alerts, Corrective/Preventive Actions (CAPA) implementation, change control and root cause analysis</li>
</ul>
<div></div><div><b>Additional Duties / Responsibilities</b><b>:</b></div>
<ul><li>Bring initiatives and activities to closure in a timely manner through effective interaction with individuals, both internal and external to the Marotta organization (as required).</li>
<li>Maintain and continue to elevate relationships with Business Development, Engineering, Operations, Customer Service and all other facets of the company</li>
<li>Abide by all safety, quality, housekeeping and company policies/procedures to ensure compliance to various regulatory and internal system requirements</li>
<li>Consistently demonstrate commitment to company values</li>
<li>Keep management informed of area activities and of any significant problems</li>
<li>Ensure that work area and work areas of direct reports are clean, secure, and well maintained</li>
<li>Complete special projects and miscellaneous assignments as required</li>
</ul>
<div></div><div><b>Work Environment</b><b>:</b></div>
<ul><li>This job interacts both in a professional office environment and a manufacturing/machine shop environment. This role uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines, as well as environments inclusive of the appropriate eye, hearing and foot protection (as required).</li>
<li>This is a full-time position. Overtime and weekend may be required as job duties demand.</li>
<li>Some travel may be expected for this position (up to 10%)</li>
</ul>
<div></div><div><b>Minimum Required Qualifications</b><b>:</b></div>
<ul><li>Bachelor of Science degree in Mechanical Engineering, Manufacturing Engineering, Aerospace Engineering or a related field of study</li>
<li>2-5 years&rsquo; experience in quality-related function</li>
<li>Work experience in data analysis and procedure writing (preferred)</li>
<li>Ability to interpret Military, Commercial aircraft and Space level specifications and standards</li>
<li>Ability to read and understand schematics and drawings</li>
<li>Knowledge of Quality Management System - AS9100, ISO9001, ISO/TS16949</li>
Knowledge of Special Processes <li>- critical finishes, chemical conversion, soldering, crimping, non-destructive and destructive analysis methods</li>
<li>Strong verbal/written communication skills required for multi-faceted interactions with all levels of personnel within the organization, as well as any and all outside agents, including but not limited to; vendors, suppliers, customers, etc.</li>
<li>Strong computer literacy, with MS Office/PC expertise, and demonstrated experience with applicable systems, programs, equipment, etc.</li>
<li>This position requires the eligibility to obtain a security clearance, therefore you must be able to obtain/maintain a security clearance</li>
<li>Must be a US Citizen</li>
</ul>
<div></div><div><b>Physical Requirements</b><b>:</b></div>
<ul><li>While performing the duties of this job, the employee is regularly required to talk and hear.</li>
<li>Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Vision and color vision must pass job-required vision screening</li>
<li>The employee is frequently required to reach with hands and arms, and to use hands to finger, handle or feel</li>
<li>The employee is regularly required to stand, sit, walk, and move about the facility.</li>
<li>The employee may be required to lift and/or move items weighing up to 25 pounds.</li>
</ul>
</div><div></div><div><div>This position is at our Montville, NJ corporate offices location.</div>
<div>Pay Range: $87,500 - $115,000</div>
<div></div><div>Many of our contracts require proof that you are a U.S. citizen and/or that an export license has been obtained for employees who are citizens of certain countries. Your employment, both initially and continually thereafter, is conditioned on production of such proof of citizenship and/or any export license that may be required to comply with any and all applicable laws, regulations, or executive orders, or required by Federal, State, or local government contracts.</div>
<div></div><div><div>We offer a highly competitive compensation package for this outstanding position plus a quarterly bonus along with a full range of top quality benefits and employee services including: medical, prescription, dental, vision, life and disability income insurance programs, 401k retirement plans with company match, generous tuition aid program, paid vacation, sick and personal days, paid holidays and flexible work hours with compressed work week options. We recognize and reward our employee's accomplishments and host several employee engagement events per quarter.</div>
<div></div><div>If you are looking to grow or accelerate your career and be part of a best in class organization while enjoying a work-life balance, please visit our website at www.marotta.com to learn more about us and to apply. Check out all our openings at https://marotta.com/job-openings/</div><br>
<div></div>
<div>We are an Affirmative Action and Equal Opportunity employer M/F/IWD/Veterans</div>
<div>VETERANS ARE ENCOURAGED TO APPLY</div>
<div></div><div><div><div><div><b>No agencies, please.</b></div></div></div></div></div></div></div><div></div>

Quality Engineer II

Bio-Rad Laboratories, Inc.

<div><div><p>As the <b>Quality Engineer, II,</b> you will support Bio-Rad&rsquo;s commitment to quality and safety by evaluating and performing activities associated with the processes that make up the Quality Management System (QMS). This includes but is not limited to: nonconforming product management and assessment, customer or CAPA investigations, process control and monitoring, products transfer, supporting process or software validations, supporting product or process improvements, change control impact assessments, and risk management.</p><br>
<p>
</p><p><b>Location: </b>This position must be based in <b>Irvine, California</b> and requires the employee to be located within commuting distance of the office.</p><br>
<p></p>
<p><b>
How You'll Make An Impact:</b></p>
<ul>
<li>Analyze nonconformances, trend information, actual and potential cause of risks to identify and recommend corrective actions and control measures.</li>
<li>Work closely with Engineering, R&amp;D, QC, SQE and other departments with customer, CAPA, or NC investigations.</li>
<li>Coordinate, support and review validation and risk management (dFMEA and/or pFMEA) activities.</li>
<li>Support product improvement projects, process changes, and/or design transfer.</li>
<li>May be assigned to other quality related tasks.</li>
</ul>
<p><b>What You Bring:</b></p>
<ul>
<li>Bachelor&rsquo;s degree or equivalent in a related technical discipline.</li>
<li>At least 2 years&rsquo; experience in regulated manufacturing industry or equivalent combination of eduction and experience.</li>
<li>Quality Engineering, Six Sigma Green or Black Belt Certification desirable.</li>
<li>Basic understanding of risk management regulations, principles and application.</li>
<li>Basic knowledge of and application of principles and theories of quality engineering.</li>
<li>Advanced understanding of GMP/ISO regulations and validation regulations is preferred.</li>
<li>Working knowledge of the device/drug/biotech manufacturing process.</li>
<li>Skilled in statistical methods, stastical process controls and sampling plans.</li>
<li>Communication, technical, and computer skills.</li>
<li>Coordination, tact, and team work.</li>
<li>Detailed-oriented and ability to multitask.</li>
</ul>
<p><b>Total Rewards Package: </b>At Bio-Rad, we&rsquo;re empowered by our purpose and recognize that our employees are as well. That&rsquo;s why we offer a competitive and comprehensive Total Rewards Program that provides value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Bio-Rad's robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee&rsquo;s work and life cycle.</p><br>
<p></p>
<p><b>
Benefits:</b> We&rsquo;re proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability, paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG&rsquo;s), and more!</p><br>
<p>
</p><p><b>Compensation: </b>The estimated base salary range for this position is $86,600 - $119,200 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is also eligible for a variable annual bonus, which is dependent upon achievement of your individual objectives and Company performance.</p><br>
<p></p>
<p><b>
Who We Are: </b>For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.</p><br>
<p></p>
<p><b>
EEO Statement: </b>Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply.</p><br>
<p></p>
<p><b>
Agency Non-Solicitation: </b>Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.</p><br>
<p></p>
<p><b>
Fraud Alert</b><b>:</b> Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake &quot;recruiters&quot; and job scams. Click here for more information on this scam and how to avoid it. #LI-AK1 #LI-Hybrid</p>
</div>
<div>Legal Entity: (USA_1000)Bio-Rad Laboratories, Inc.</div></div>

Fastener Distribution Holdings

<div><p><b>Who Are We?</b></p><p>
FDH Aero is a trusted global supply chain solutions partner for aerospace and defense companies, helping to shape the industry by simplifying the supply chain. With over 60 years serving as a leading independent industry partner, FDH specializes in hardware, electrical, consumables and expendables, licensed products, and value-added services for global OEM and aftermarket customers. FDH is headquartered in Commerce, California, and has operations across the Americas, EMEA and APAC. FDH Aero &ndash; named a Best Places to Work in Aviation in 2024 &ndash; has locations in 14 countries across the globe, with more than 1,500 best-in-industry employees and over 650,000 square feet of inventory space.</p><p>
FDH is headquartered in Commerce, California, and has operations across the Americas, EMEA and APAC. FDH Aero &ndash; named a Best Places to Work in Aviation in 2024 &ndash; has locations in 14 countries across the globe, with more than 1,500 best-in-industry employees and over 650,000 square feet of inventory space.</p><p></p><p><b><br>
Why Work Here?</b></p><p>
At FDH Aero, we understand that the strength of our brand comes from our people.</p><p>
We invest in driven, diverse and experienced professionals who are naturally curious, courageous and motivated towards action. We value tempering confidence with humility, and a mission that always starts with service-first.</p><p>
Our values guide everything we do:</p><p><b>
We Are Service First</b> - We act with agility and intelligence to solve our partner&rsquo;s most pressing needs. We safeguard our trusted relationships by communicating with clarity and unmatched follow through.</p><p><b>
We Are Respectful</b> - We behave with dignity, fairness, and acceptance. We thrive by prioritizing empathy, humility, and connection to our collective community.</p><p><b>
We are Amplifiers</b> - We invest in driven, diverse and experienced professionals, businesses and partners. We fuel the entrepreneurial spirit by providing autonomy, authority and a clear mission.</p><p><b>
We Are Open-Minded</b> - We communicate with intention, curiosity, and diversity of thought. By actively contributing with courage and candor, we challenge the status quo and innovate together.</p><p><b>
We Are Accountable</b> - We own responsibility for our outcomes. We set expectations, embrace critique, and empower every employee to take immediate actions on challenges they encounter.</p><p><b>
We Value Our People</b> - That&rsquo;s why we offer competitive benefits, including medical, dental, vision, Flexible Spending Accounts (FSA), 401k matching, and wellness programs. We invest in training, mentorship, and career development to empower our employees to reach their full potential. Our commitment to culture and excellence has earned us recognition as one of Aviation Business News' Best Places to Work in Aviation.</p><p>
As a team member at FDH Aero you are trusted to deliver, to innovate, and to drive next-generation solutions for tomorrow&rsquo;s supply chain demands. Ready to make an impact? We proudly pursue top talent with a diverse and global set of experiences and backgrounds.</p><p></p><p><b><br>
We Are Looking For</b></p><p>
The Quality Engineer II will support and enforce the quality control systems to ensure standards are established, achieved, and maintained to meet the requirements of the Company, Industry, and Customer standards. They will be the focal point for interfacing Quality Assurance issues with internal and external customers and suppliers, ensuring compliance to the appropriate requirements including non-conformance analysis and implementation of effective countermeasures.</p><p></p><p><b><br>
What You'll Do (Responsibilities)</b></p><ul><li>
Establish and communicate facility audits to include internal, customer, and 3rd registrar audits</li><li>
Establish and maintain the organization&rsquo;s audit guidelines</li><li>
Facilitate audit activities with 3rd party auditors, customers, and internal team members to include pre-briefings, kick off, and debriefings</li><li>
Document audit findings and observations using corrective actions and ensure team members complete required actions</li><li>
Establish clear criteria to measure supplier performance and recommend the appropriate actions for suppliers that excel (skip lot), or fall short (corrective actions, audits etc)</li><li>
Communicate with vendors as needed to improve performance, resolve issues and support internal teams</li><li>
Work with cross-functional teams to determine primary issues for customers, and primary reason for returns with suppliers to drive improvement and increase performance</li><li>
Prioritize actions using methodologies including Voice of Customer (VOC), Measurement Systems Assessment (MSA), Failure Mode Analysis (FMEA), Cause and Effect (C&amp;E), and Control Parameter Management (CPM)</li><li>
Utilize appropriate quality analysis tools to review the quality processes to drive improvement and ensure continued compliance with customer requirements, specifications, and quality performance expectations</li><li>
Schedule and track Inspection and Quality activities to achieve maximum effectiveness and efficiency</li><li>
Ensure a high level of internal and external customer service by investigating and correcting customer issues and complaints</li><li>
Regularly report customer and supplier quality metrics such as First Time Quality performance and internal / external defect rates</li><li>
Contribute to team effort by working cross functionally to deliver the desired results for the business</li><li>
Perform other duties as assigned</li></ul><p></p><p><b><br>
What You Bring (Qualifications &amp; Skills):</b></p><ul><li>
Bachelor's degree in Aerospace Engineering, Manufacturing, Mechanical, Industrial, Structural, Systems, or related field from an Accredited Institution</li><li>
3-5 Years in distribution, manufacturing, or Supply Chain</li><li>
Experience working in Aerospace quality systems preferred</li><li>
Ability to understand and interpret engineering technical data, such as manufacturing or part drawings, to provide guidance to cross-functional teams.</li><li>
Significant experience working directly with customers and suppliers</li><li>
Must have excellent written and verbal communication skills, as well as strong problem solving, organizational, project management and decision-making skills</li><li>
Understand internal and external customer requirements with a high attention to detail in resolving findings</li><li>
Knowledge of aerospace quality standards</li><li>
Ability to process and effectively communicate information using MS 365 Suite of tools (i.e., PowerPoint, Excel, and Word)</li></ul><p></p><p><b><br>
Special Requirements:</b></p><ul><li><b><i>
U.S. Citizen, U.S. Permanent Resident (Green Card holder) or </i></b><i>asylee/refugee status as defined by 8 U.S.C. 1324b(a)(3) required.</i></li><li>
ITAR requirement</li><li><i>
120.15. Some positions will require current U.S. Citizenship due to contract requirements.</i></li></ul><p><i>
This position requires access to information that is subject to compliance with the International Traffic Arms Regulations (&ldquo;ITAR&rdquo;) and/or the Export Administration Regulations (&ldquo;EAR&rdquo;). In order to comply with the requirements of the ITAR and/or the EAR, applicants will be asked to provide specific documentation to verify U.S. person status under the ITAR and the EAR. A &ldquo;U.S. person&rdquo; according to their definition is a U.S. citizen, U.S. lawful permanent resident (green card holder), or protected individual such as a refugee, or asylee. See 22 CFR</i></p><p></p><p><b><br>
FDH Aero</b> is an Equal Opportunity Employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.</p></div>

Cadrex Manufacturing Solutions

<div>Description:
<p>
OVERVIEW</p><p>
Cadrex is searching for a Quality Engineer III to Implement and maintain engineering and quality process including ensuring quality of manufactured goods from delivery of raw materials to final product by continually assessing process and recommending improvements. Works closely with other departments to ensure continuity in production, efficiency, quality, and safety.
</p><p>KEY RESPONSIBILITIES</p><ul><li>
Design, document and implement methods for process control (including SPC), process improvement, testing and inspection</li><li>
Conduct root cause analysis as needed, utilizing applicable tools to ensure robust solutions or improvements are determined and implemented</li><li>
Manage large projects to ensure timelines are met and appropriate resources have proper communication and direction</li><li>
Conduct internal quality system audits</li><li>
Facilitate and lead CAPA meetings, follow up on corrective actions to ensure CAPA&rsquo;s are being resolved in a timely manner?</li><li>
Lead appropriate advanced product quality planning (APQP) processes within the organization to ensure product and process validation and verification?</li><li>
Develop and maintain tools for Quality System metric reporting. Ensure metrics are being reported accurately</li><li>
Work with engineering team using past performance data to prevent future occurrences. Utilize tools such as DOE, DFM, FMEAs, GD&amp;T, process capability, 6-sigma designs, etc.?</li><li>
Assist disposition process by involving in failure analysis and suggest corrective actions as Material Review Board member</li><li>
Lead and develop New Employee Orientation Blue Print Reading Training and develop and implement programs needed for additional quality new employee training in coordination with the Human Resources Department</li></ul>
Requirements:
<p>
PREFERRED QUALIFICATIONS</p><ul><li>
Preference of 5-7 years recent, relevant experience in a manufacturing environment</li><li>
Strong understanding of manufacturing processes and tooling</li><li>
Experience in Medical Systems and Audits (ISO 13485) preferred</li><li>
A strong knowledge of ISO 9001 Quality Systems and audit requirements
</li><li>Auditing experience preferred</li></ul><p>
EDUCATION</p><ul><li>
Bachelor&rsquo;s degree in engineering and/or Certified Quality Engineer preferred</li></ul><p>
LOCATION</p><ul><li>
Onsite</li></ul><p>
SCHEDULE</p><ul><li>
M-F</li></ul><p><b>
TOTAL COMPENSATION INCLUDES</b></p><ul><li>
Health/dental/vision coverage</li><li>
Employer-paid and supplemental life insurance</li><li>
Short- and long-term disability insurance</li><li>
Generous paid time off and holiday pay</li><li>
Monthly remote work stipend (for remote employees who qualify)</li><li>
401(k) investment plan, with an employer match of up to 4%</li><li>
Education support program</li><li>
Safety eyeglasses/shoe reimbursement</li><li>
Referral bonuses</li><li>
Bonus plan for all full-time employees</li></ul><p>
 WORK ENVIRONMENT</p><ul><li>
While performing the duties of this job, the employee is frequently exposed to work near moving mechanical parts and vibration. The employee is occasionally exposed to the risk of electrical shock. The noise level in the work environment is usually moderate and occasionally loud.</li></ul><p>
PHYSICAL DEMANDS</p><ul><li>
While performing the duties of this job, the employee is regularly required to stand, sit, use hands and fingers, handle or feel, and talk or hear. The employee is occasionally required to sit; climb or balance; stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, color vision, depth perception and ability to adjust focus.</li></ul><p>
CADREX&rsquo;S CORE VALUES</p><ul><li>
Safety first, rising to the challenge, collaboration, accountability, and doing the right thing</li></ul><p>
ABOUT US</p><p>
CADREX Manufacturing Solutions is a leading provider of complex sheet metal and machined production parts, assemblies, and weldments for a variety of end markets, including electrical transmission and distribution, warehouse automation, technology, aerospace &amp; defense, medical, food, and industrials. With locations in Colorado, Pennsylvania, Illinois, Washington, Wisconsin, Minnesota, Michigan, Indiana, Massachusetts, Oklahoma, and Monterrey Mexico, CADREX offers numerous in-house manufacturing capabilities, including laser cutting, sheet metal fabrication, complex assembly, CNC punching, CNC machining, forming, robotic welding, stamping, fastener insertion, and tool and die manufacturing, to effectively serve customers with lights-out manufacturing capabilities for mid- to high-volume production. For more information, visit www.cadrex.com.</p><p>
Cadrex provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.</p></div>

Engineer III - Quality

Trading & Construction Group

<p>QA/QC Engineer &ndash; Job Description</p><p><b>QA/QC Engineer</b></p><p>2. Location</p><p>Project sites across Qatar</p><p>3. Job Summary</p><p>The QA/QC Engineer is responsible for <b>implementing quality assurance and quality control procedures</b> to ensure that all project activities comply with <b>project specifications, international standards, and client requirements</b>. The role involves inspections, documentation control, testing coordination, and ensuring compliance with approved quality plans.</p><p>Key ResponsibilitiesQuality Assurance</p><ul><li>Develop and implement <b>Quality Management System (QMS)</b> for the project.</li><li>Prepare and review <b>Inspection and Test Plans (ITP)</b>.</li><li>Ensure compliance with <b>ISO standards such as International Organization for Standardization quality guidelines (e.g., ISO 9001)</b>.</li><li>Conduct <b>internal audits and quality reviews</b>.</li></ul><p>Quality Control</p><ul><li>Perform <b>site inspections and material inspections</b>.</li><li>Monitor construction activities to ensure compliance with <b>approved drawings and specifications</b>.</li><li>Review <b>method statements, material submittals, and shop drawings</b>.</li><li>Raise <b>Non-Conformance Reports (NCR)</b> when quality issues occur.</li><li>Follow up on <b>corrective and preventive actions</b>.</li></ul><p>Documentation &amp; Reporting</p><ul><li>Maintain <b>quality records, inspection reports, and test reports</b>.</li><li>Coordinate with consultants and clients for <b>inspection requests (IR)</b>.</li><li>Prepare <b>daily/weekly quality reports</b>.</li></ul><p>Testing &amp; Compliance</p><ul><li>Coordinate <b>material testing with approved laboratories</b>.</li><li>Ensure materials comply with project specifications and standards.</li><li>Verify calibration of testing equipment.</li></ul><p>Coordination</p><ul><li>Work with <b>project managers, site engineers, and subcontractors</b>.</li><li>Attend <b>quality meetings with consultants and clients</b>.</li></ul><p>Qualifications</p><ul><li><b>Bachelor&rsquo;s degree</b> in Civil Engineering / Mechanical Engineering / Electrical Engineering or related field.</li><li><b>3&ndash;8+ years of experience</b> in QA/QC in construction or oil &amp; gas projects.</li><li>Certification in <b>ISO 9001 Quality Management Systems</b> is often preferred.</li><li>Knowledge of <b>international standards such as ASTM International, American Society of Mechanical Engineers, and American Concrete Institute</b> (depending on discipline).</li><li>Strong understanding of <b>inspection procedures and quality documentation</b>.</li></ul><p>Key Skills</p><ul><li>Quality management systems</li><li>Construction inspection</li><li>Technical documentation</li><li>Problem-solving and root cause analysis</li><li>Communication and reporting</li><li>Knowledge of <b>NCR, RFI, MIR, and ITP processes</b></li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

QA/QC ENGINEER

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