Quality manager jobs in Palm Desert, CA - 42 jobs

JOB TITLE: Quality Assurance Manager PAY RATE: $75/hour We are a national aerospace and defense staffing agency seeking highly qualified candidates for a position with a top-tier client. Job Details: Job Type: Contract (12 months with potential for extension) Industry: Aerospace / Defense / Aviation Benefits: Medical, dental, and vision (Cigna) Perks: Bonus potential + Priority access via Tier 1 supplier Openings Nationwide: Thousands of opportunities across the U.S. Qualifying Questions: Are you a U.S. person as defined under ITAR regulations? Do you meet the educational and experience requirements for this role? Can you commute to the job location or relocate if necessary? Summary: Regulatory compliance (FAA, AS9100, DCMA) Leadership and development of quality teams Oversight of inspection, documentation, and airworthiness activities Continuous improvement and audit readiness Requirements: Minimum of 7 years of related experience within a 14 CFR Part 145 Repair Station, with exposure to 14 CFR Part 21 PAH or AS9100 aerospace manufacturing environments At least 5 years of leadership experience managing and developing teams Bachelor's or Associate's degree in a related field preferred FAA Airframe and/or Powerplant (A&P) license required FAA Inspector Authorization (IA) strongly preferred Strong working knowledge of Federal Aviation Regulations, airworthiness directives, and approved maintenance and alteration data Demonstrated ability to provide direction while collaborating effectively with management teams Experience with DCMA flight and ground operations compliance preferred Proven ability to lead and manage a team of quality professionals in a goal-driven environment Ability to read and interpret technical data, repair manuals, and engineering drawings In-depth knowledge of FAA regulations, including 14 CFR Parts 21, 43, 65, 91, and 145 Experience researching and interpreting aircraft historical records and logbooks Excellent verbal and written communication skills Strong work ethic with a high level of organization and attention to detail Must be a U.S. Citizen (as defined by ITAR). About Us: The Structures Company is a premier national aerospace and defense staffing agency specializing in contract, contract-to-hire, and direct hire placements. We deliver expert workforce solutions across engineering, IT, production, maintenance, and support roles. As trusted partners to major aerospace OEMs and Tier 1 suppliers, we connect professionals with opportunities to grow and excel in the aviation and aerospace industries. Eligibility Requirements: Must be a U.S. Citizen, lawful permanent resident, or protected individual under 8 U.S.C. 1324b(a)(3) to comply with ITAR regulations. Keywords: aerospace, aviation, engineering, maintenance, aircraft design, defense Take your career to new heights-apply today!

GARNEY CONSTRUCTION A Quality Control Manager position in Location is available at Garney Construction. Join our Garney team to manage and support project Quality Management Specialists, ensuring each project is successful. The Quality Control Manager is responsible for the implementation, management, and execution of Quality Management Programs for Federal contracting projects. WHAT YOU WILL BE DOING Develop and implement project Quality Management Systems to ensure compliance with contract quality standards Review project CPM schedule to anticipate and request timely submittals Review project schedules and prepare Government meeting notices to support schedules Conduct weekly Quality Control meetings Perform/supervise quality inspections as needed by the project or Project Manager Provide effective and efficient communication with the Federal Government personnel Promote Garney's safety programs and procedures to promote a safe working environment WHAT WE ARE LOOKING FOR 10 years of construction experience, 3 years being Construction Quality Manager experience Bachelor's Degree in Engineering, Construction Management, or related field Current USACOE Construction Quality Management for Contractors Certification EM 385 40 hour and OSHA 30-hour certifications LET'S TALK THE PERKS! Salary Range - $136,200-$154,300 Employee Stock Ownership Plan (ESOP) 401K Retirement plan Health, dental, vision and life insurance Flexible Spending Account (FSA) / Health Savings Account (HSA) Long-term disability Wellness program Employee Assistance Plan Holidays and PTO Bonus program CONTACT US If you have questions about the position, please contact Patrick Duque at ************************ . Please include resumes, references, job lists, and any other relevant documentation. Garney Construction and its subsidiaries are committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Garney Construction is a background screening, drug-free workplace. Agency Disclaimer: All vendors must have a signed Garney Construction Agreement, authorized by the Executive Team, to receive payment for any placement. Verbal or written commitments made by anyone other than a member of the Executive Team will not be considered binding. Any unsolicited resumes sent to Garney Construction or submitted to employees outside of the Recruiting Team will be deemed the property of Garney Construction. In such cases, Garney Construction will not be obligated to pay any placement fees.

Twentynine Palms Microgrid Project CLP Engineering, LLC (CLPE) is assembling a project-specific team to deliver a NAVFAC Microgrid project at Marine Corps Air Ground Combat Center (MCAGCC) in Twentynine Palms, California. We are seeking an experienced Contractor Quality Control (CQC) System Manager to lead and enforce the project's quality control program in full compliance with NAVFAC contract requirements, Division 1 specifications, and federal construction standards. This is a site-dedicated role with full authority over quality control activities, including work stoppage when necessary. CLPE is a full-service electric utility solutions engineering firm with more than twenty years' experience in electrical utility system ownership, upgrades, maintenance and operations through our sister company, City Light & Power. CLPE offers a wide range of power system engineering services to investor-owned, municipal, cooperative, government, industrial, and commercial customers. City Light & Power/CLP Engineering has been recognized by The Denver Post as one of the top workplaces for 2025! Duties and Responsibilities: Participate in pre-construction meetings, schedule meetings, design reviews, and project kickoff meetings to provide input on quality control requirements and expectations. Submittal creation and tracking. Develop, schedule, and implement procedures for tracking control phase meetings required for the three-phase control system. Review project documentation, including drawings, specifications, and submittals to ensure adherence throughout the project lifecycle. Coordinate with project managers, engineers, superintendents, safety officers, subcontractors, and suppliers to address quality issues and non-conformances promptly and effectively. Monitor subcontractor and supplier performance with respect to timeliness, efficiency, and quality. Conduct regular inspections and audits of construction sites to monitor compliance with quality control standards, specifications, and codes. Assist with providing training and guidance to project teams on quality control procedures, best practices, and regulatory requirements. Document and report quality control activities, findings, and corrective actions to project stakeholders and management. Participate in monthly project review meetings to discuss schedule, quality control metrics, challenges, and opportunities for improvement. Coordinate with project management to ensure all close-out documents are complete and submitted. Other duties as assigned. *Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Skills, Knowledge, Qualifications, & Experience: Degreed professional with a minimum of 5 years of construction experience on similar projects OR Construction professional with 10 years of related quality management experience Bachelor's degree in engineering, construction management, or related field preferred. USACE Construction Quality Management (CQM) for Contractors - completed within the last 5 years OSHA 30 Certified EM 385-1-1 Training Extensive experience with USACE or federal construction projects Extensive experience with USACE, NAVFAC, or federal construction projects Strong knowledge of USACE/NAVFAC QC procedures, eCMS, and Three-Phase Control Proven ability to work in a team environment and manage multiple tasks simultaneously. Supervisory Responsibility: May supervise QC staff depending on project. Position Type/Expected Hours of Work: This is a full-time exempt position. Office hours of work are Monday through Friday. The ability and availability to travel, attend meetings and functions outside typical business hours required. Travel: Full time on a project site with up to 20% overnight travel to other job sites Work Authorization/Security Clearance: You must be a US Citizen. Military Base Access Security Clearance is required for this position. A valid driver's license is required. Benefits & Compensation: We offer an excellent benefits package that includes medical insurance, dental insurance, life insurance, short and long term disability, 401k with company contribution, paid time off and paid holidays. Salary range: $100,000 - $130,000 /annual based on experience plus eligible to participate in Short Term Incentive Plan. We reserve the right to pay more or less than the posted salary range based on factors unrelated to sex. To learn more, visit our website: *********************** We are proud to be an EEO/AA employer M/F/Disabled/Veterans. We maintain a drug-free workplace and perform pre-employment substance abuse testing.

Job Description Quality Control Manager (QCM), Federal Construction Columbus, GA Full-Time, Onsite, Federal Project Assignment About the Role We are seeking an experienced Quality Control Manager (QCM) to support federal government construction projects in the Columbus, GA area. This role is critical to ensuring all construction activities comply with contract documents, USACE standards, EM 385 requirements, and applicable federal regulations. The QCM will serve as the primary point of contact for quality-related matters and will work closely with the Project Manager, Superintendent, subcontractors, and government representatives. Key Responsibilities Develop, implement, and manage the Contractor Quality Control (CQC) Plan in accordance with USACE and DoD requirements Conduct and document the Three-Phase Control Process: Preparatory, Initial, and Follow-Up Inspections Review and manage submittals, RFIs, and quality documentation for compliance with contract specifications Perform daily quality control inspections across all phases of construction including civil, structural, architectural, and MEP work Prepare and submit daily QC reports, inspection logs, deficiency tracking, and corrective action documentation Coordinate and lead preparatory meetings, initial inspections, and quality coordination meetings Interface directly with Government QA personnel and participate in inspections, audits, and site walks Ensure work is executed in accordance with approved plans, specifications, and safety standards Track deficiencies, oversee corrective actions, and verify closeout compliance Support project closeout activities including punch lists, as-builts, and final inspections What We're Looking For Minimum 5 years of experience as a Quality Control Manager on federal construction projects Demonstrated experience working on USACE, NAVFAC, or other DoD projects Strong knowledge of federal construction standards, quality processes, and documentation requirements Experience coordinating with government inspectors and contracting officers Ability to manage multiple features of work and maintain organized quality records Strong communication skills and attention to detail Required Certifications & Qualifications USACE Construction Quality Management (CQM) for Contractors Certification OSHA 30-Hour Construction Safety Certification Working knowledge of EM 385-1-1 safety standards Ability to pass federal background requirements and site access credentials Valid driver's license Why Join Us? Work on stable, long-term federal government construction projects Clear scope, defined quality standards, and structured project environments Opportunity to work with experienced federal project teams Competitive compensation based on experience and certifications Total Rewards & Benefits Competitive salary or hourly compensation based on experience Per diem, lodging, and travel support if applicable Health insurance options and paid time off Consistent federal project pipeline Apply Today Qualified candidates are encouraged to apply to be considered for current and upcoming federal construction projects in the Columbus, GA area. Confidential inquiries are welcome.

This position shall have overall responsibility for the contractor's quality control management program to include maintaining and overseeing the quality control management program for entire contract.  Primary Job Functions: Administer quality control management program Responsible for overall quality assurance program Monitor and inspect all delivery orders for compliance Maintain records of inspections and certifications Prepare monthly reports depicting findings of quality inspections Periodically review the quality control program to ensure compliance Examine processes for preventative and corrective maintenance; make suggestions based on findings Perform inspections and re-inspections to ensure problems have been resolved Collect data for the DMLSS system including work orders and equipment history Research safety and quality topics online May prepare incident and accident reports May be tasked with preparing training materials and conducting employee safety meetings May manage the disposal of hazardous waste May research and issue infection control and interim Life Safety permits May train personnel on material control and equipment and tool management Other duties as assigned Education, Experience and Certification: Required: Associate degree Required: 5 years of experience in preparing and enforcing quality management programs (QMS) on similar size, scope and complexity. Preferred: OSHA certification Knowledge, Skills, and Abilities: Knowledge of OSHA safety regulations and PPE procedures Ability to conduct accident investigations and safety inspections Strong written and oral communication skills Financial Responsibilities: Determine if the role has the authority over budget or revenue. If so, you must describe in what manner in the description box. Travel Requirements: 10% Disclaimer: CBRE Government & Defense Services are thrilled at the opportunity for you to apply for one of our roles. The base salary range for this position is $55,000- $82,000. This position may also be eligible for a wide range of competitive benefits that can include but are not limited to medical, well-being, financial planning and short-term benefits. This description is not intended to be an “all inclusive” list of the accountabilities of the job described. Rather, it describes the general nature of the job. In addition, some aspects of this job may change over time, according to business needs, and these changes may not be recorded immediately. The requirements stated represent the minimum levels of knowledge, skills and/or abilities to qualify and satisfactorily perform this job. THIS DOCUMENT SHOULD NOT BE CONSTRUED AS CREATING A CONTRACT OF EMPLOYMENT BETWEEN CBRE GOVERNMENT & DEFENSE SERVICES AND ANY OF ITS EMPLOYEES OR OTHERWISE ALTERING AN EMPLOYEE'S AT WILL EMPLOYMENT RELATIONSHIP WITH CBRE GOVERNMENT & DEFENSE SERVICES.

Job Description This position shall have overall responsibility for the contractor's quality control management program to include maintaining and overseeing the quality control management program for entire contract. Primary Job Functions: Administer quality control management program Responsible for overall quality assurance program Monitor and inspect all delivery orders for compliance Maintain records of inspections and certifications Prepare monthly reports depicting findings of quality inspections Periodically review the quality control program to ensure compliance Examine processes for preventative and corrective maintenance; make suggestions based on findings Perform inspections and re-inspections to ensure problems have been resolved Collect data for the DMLSS system including work orders and equipment history Research safety and quality topics online May prepare incident and accident reports May be tasked with preparing training materials and conducting employee safety meetings May manage the disposal of hazardous waste May research and issue infection control and interim Life Safety permits May train personnel on material control and equipment and tool management Other duties as assigned Education, Experience and Certification: Required: Associate degree Required: 5 years of experience in preparing and enforcing quality management programs (QMS) on similar size, scope and complexity. Preferred: OSHA certification Knowledge, Skills, and Abilities: Knowledge of OSHA safety regulations and PPE procedures Ability to conduct accident investigations and safety inspections Strong written and oral communication skills Financial Responsibilities: Determine if the role has the authority over budget or revenue. If so, you must describe in what manner in the description box. Travel Requirements: 10% Disclaimer: CBRE Government & Defense Services are thrilled at the opportunity for you to apply for one of our roles. The base salary range for this position is $55,000- $82,000. This position may also be eligible for a wide range of competitive benefits that can include but are not limited to medical, well-being, financial planning and short-term benefits. This description is not intended to be an “all inclusive” list of the accountabilities of the job described. Rather, it describes the general nature of the job. In addition, some aspects of this job may change over time, according to business needs, and these changes may not be recorded immediately. The requirements stated represent the minimum levels of knowledge, skills and/or abilities to qualify and satisfactorily perform this job. THIS DOCUMENT SHOULD NOT BE CONSTRUED AS CREATING A CONTRACT OF EMPLOYMENT BETWEEN CBRE GOVERNMENT & DEFENSE SERVICES AND ANY OF ITS EMPLOYEES OR OTHERWISE ALTERING AN EMPLOYEE'S AT WILL EMPLOYMENT RELATIONSHIP WITH CBRE GOVERNMENT & DEFENSE SERVICES.

We are seeking a detail-oriented and driven Quality Engineer I to join our team. In this role, you will support quality assurance processes, drive continuous improvement initiatives, and ensure our products meet and exceed customer expectations. This is an exciting opportunity to make a meaningful impact and grow your career in quality engineering. Come join our growing team! Primary Duties & Responsibilities The Quality Engineer I: Performs moderately complex tasks to develop, apply, and maintain quality requirements for processing components and other materials into finished goods and products. Plans the quality measurements and controls on materials, processes, and product to provide adequate control of quality at minimum quality related costs. Analyzes quality information and feeds back analyses and recommendations for adjustment to product design, manufacturing process and equipment, and the quality system. Applies statistical methods to diagnose and correct improper quality practices, workmanship and process problems. On behalf of the Quality Manager, carries out essential steps in maintaining the company quality system. Quality Planning - 20% Recommends Quality objectives and goals in line with company Thrusts and Initiatives. Works with Quality Management, Marketing, Engineering and Customers in establishing specific quality requirements on individual products based upon customer requirements. Reviews contracts for manufacturing quality ability. Plans quality measurements and controls sufficient to provide adequate control of quality at minimum quality related costs. Applies and maintains Quality Standards for processing materials into partially finished or complete products. Assists Quality Management in determining and establishing the required quality procedures for controlling product quality. This planning includes the relative importance of quality characteristics and required quality levels; points in the flow for quality measurements to be made; methods and procedures for quality measurements by operators, inspectors, testers, and auditors; applicable Statistical Quality Control techniques; Quality Information feedback; required quality measurement and control equipment; and other pertinent quality procedures. Assures incorporation of applicable quality measurements into the manufacturing process and documentation. Defines and communicates quality requirements to Suppliers through Purchasing documents. Works with Manufacturing Engineering and Production to incorporate, where possible, the quality measurement and control devices with the production equipment to provide optimum mechanization and automation through integrated analysis and feedback of quality data. Promotes Continuous Improvement and Provides Customer Service - 10% Reviews product specifications and makes changes as necessary to assure a consistent product that meets or exceeds customer requirements. Appraises the nature of production quality problems, customer complaints and economical operations. Diagnoses chronic manufacturing quality problems. Identifies root causes, recommends and implements improvements and corrective/preventive actions. Analyzes, identifies basic causes, and feeds back analyses and recommendations regarding customer complaints. Participates with others in instigating corrective action. Follows-up and reports on corrective action progress to Quality Management. Performs failure analyses (FMEA), as needed, to reduce rejects and production problems. Acts as a primary interface with Government representatives (DCMAO) and customer source inspection personnel. Coordinates government and customer source inspections and Quality system surveys. Resolves issues with customers on warranty returns in a timely manner. Provides Support to Quality Control, Sales, Engineering, and Operations - 30% Reviews prints and quotes for QA requirements as necessary in a timely manner. Provides technical assistance to other departments. Maintains cognizance of customer and internal Engineering changes and procedural changes to assure accurate and up-to-date documentation is available to appropriate individuals at all times. Discusses quality issues and specifications with customer source and quality representatives as necessary. Provides assistance in the application of statistical methods to diagnose and correct improper quality practices, workmanship and process problems. Provides Production and Inspection areas all necessary interpretations of the quality requirements for inspection: their use, operation, and intent. Initiates and reviews Receiving Inspection and Test Records (RITR's). Writes Quality Assurance Instructions as required . Recommends and documents incoming inspection methods, in- process and final testing methods. Nonconforming Material Control - 40% Participates in the Material Review Board. Maintains segregation of nonconforming material. Processes Deviation Requests. Coordinates with Customers, Program Management and Sales to ensure that all products are acceptable before shipment. Processes Quality Improvement Requests, supplier deviation requests and waivers. Investigates nonconforming materials, components, and product for causes. Works closely with Quality Management, Production Control, Manufacturing, Engineering and Assembly for prompt and economic disposition and correction of the causes of nonconformities. Processes and codes NCMR's with applicable defect, cause and corrective action codes. Evaluates history for trends, etc. Education & Experience Minimum 2 years of related experience in one or more branches of Quality Assurance BS/MS in Quality Technology, Engineering, Mathematics, the Basic Sciences or equivalent degree. Skills Strong skills in inspection, writing, interpersonal communications Knowledge of Quality Assurance, Engineering, and Statistical Methods Good interpersonal skills and ability to work with challenging customers and suppliers Understanding Mil-Specs, ANSI, ISO etc. Skilled with interferometers, spectrophotometers, calipers, micrometers, Coordinate Measurement Machines, lasers and electronic test equipment American Society for Quality Certification as a Quality Engineer is a plus Lead auditor experience is a plus Working Conditions Lab and Office Environment Physical Requirements Standing. Particularly for sustained periods of time. 25% of the time. Walk. Occasionally move about inside the office to access file cabinets, office machinery, etc. Talking. Expressing or exchanging ideas by means of the spoken word. Those activities in which they must convey detailed or important spoken instructions to other employees accurately, loudly, or quickly. Hearing. Perceiving the nature of sounds at normal speaking levels with or without correction. Ability to receive detailed information through oral communication, and to make the discriminations in sound. Lifting. Raising objects from a lower to a higher position or moving objects horizontally from position-to-position. This factor is important if it occurs to a considerable degree and requires substantial use of upper extremities and back muscles. No more than 10 to 15 pounds. Safety Requirements All employees are required to follow the site EHS procedures and Coherent A&D EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent A&D: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent A&D is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. This role involves access to technology, materials, software, or hardware subject to U.S. export control laws. Therefore, to be considered, candidates must be classified as a “U.S. Person” under applicable regulations or be eligible for authorization under a U.S. government export license.

Primary contact for engineering support of In-Process Inspectors. Support production efforts and process improvements (trend analysis, process validation, SPC). Coordinate In-Process MRB acitvities. Support Quality Systems (perform audits, SOP improvement, training, CAPA investigations). Ensure from the Quality prospective the transfer of new products from R&D to Production. Support Statistical Techniques and SPC interpretation. Present PPR and Management Review. 0-1 years of industry experience in ISO-9001 environment, preferably medical device. Bachelor of Science or higher degree in ME, IE or equivalent. BS degree required in either engineering or a related scientific field. This will be for a line support engineer

The Lab Services Quality Engineer is responsible for ensuring quality by design, ensuring that method development and execution is always conducted in compliance with laboratory quality and compliance standards. S(he) supports technical data review and ensures data and documentation generated meet cGMP requirements. The Lab services Quality Engineer closely collaborates with Technology Development and Operations functions and acts as the technical lead within QA department to work with engineering on review of engineering drawings, data analysis, reporting and investigations S(he) ensures the maintenance and enhancement of the company's Quality Management System (QMS), with a focus on continuous improvement and operational excellence. **Job Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a **maker of possible** with us. **Key Responsibilities:** + Lead and implement design verification testing activities for combination products in accordance with FDA 21 CFR part 210,211, 820, ISO/IEC 17025 and ISO 13485 + Develop and review test protocols, methods, and reports to ensure compliance with design control and risk management requirements. + Collaborate with cross-functional teams including technology development, operations and business development to support flawless project execution and delivery management. + Ensure laboratory compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). + Support root cause investigations, CAPA, OOS/OOT and non-conformance resolution related to design verification testing. + Provide technical guidance and mentorship to junior engineers and laboratory staff. + Participate in internal and external audits, including regulatory inspections. + Maintain and improve quality systems, including CAPA, Nonconformances, calibration and maintenance and equipment qualification. + Stay ahead of evolving regulatory expectations for combination products and contribute to continuous improvement initiatives. **Data Review & Project Release** + Conduct timely reviews of project documentation including but not limited to protocol, laboratory data, audit trails, and reports prior to release to the client + Quality Management System ** ** **Execution and maintenance of QMS activities including:** + Provide problem solving and root cause analysis expertise to lead / support OOS/Deviation/CAPA investigations + Review Test Method Validation and provide quality expertise in the development of test methods and protocols + Act as technical QA representative during audits + Compliance & Continuous Improvement + Identify and drive implementation of improvements in current quality systems and processes. + Achieves Key Performance Indicator (KPI) objectives by helping develop the appropriate production/quality data collection process, collecting data (including nonconformance, OOS, OOT, CAPAs, Deviations), and conducting the appropriate trending analysis to allow for the appropriate continuous improvement strategic plans to be enacted. + Prepare and present quality reports and metrics to senior management + Support ZebraSci QMS integration into BD Quality Global procedures and systems. + Train and guide staff in quality procedures and compliance. **Education and Experience** + Bachelor's or master's degree in engineering, Biomedical Sciences, or related field. + Minimum 5 of experience in quality engineering, preferably in a combination product or medical device environment. + Strong knowledge of design control, risk management (ISO 14971), and verification/validation principles. + Demonstrated knowledge and experience in executing CAPA, with knowledge of investigation tools, problem solving process and methodology + Experience with mechanical and analytical testing of drug-device combination products. + Familiarity with 21 CFR Part 820, 21 CFR Part 4, and ISO 13485. + Excellent analytical, organizational, and communication skills. + Proficiency in statistical analysis tools and quality engineering methodologies (e.g., Gage R&R, DOE, FMEA). + Experience with Laboratory Information Management Systems (LIMS) a plus. + Experience managing or participating in audits a plus. Salary ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary offered to a successful candidate is based on experience, education, skills, and actual work location. Salary ranges may vary for Field-based and Remote roles. $80,600.00 - $133,000.00 USD Annual At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. **Why Join Us?** A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . **Primary Work Location** USA CA Temecula **Additional Locations** **Work Shift** At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You (********************************************* . Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles. **Salary Range Information** $80,600.00 - $133,000.00 USD Annual Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

SummaryThe Lab Services Quality Engineer is responsible for ensuring quality by design, ensuring that method development and execution is always conducted in compliance with laboratory quality and compliance standards. S(he) supports technical data review and ensures data and documentation generated meet cGMP requirements. The Lab services Quality Engineer closely collaborates with Technology Development and Operations functions and acts as the technical lead within QA department to work with engineering on review of engineering drawings, data analysis, reporting and investigations S(he) ensures the maintenance and enhancement of the company's Quality Management System (QMS), with a focus on continuous improvement and operational excellence.Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Key Responsibilities: Lead and implement design verification testing activities for combination products in accordance with FDA 21 CFR part 210,211, 820, ISO/IEC 17025 and ISO 13485 Develop and review test protocols, methods, and reports to ensure compliance with design control and risk management requirements. Collaborate with cross-functional teams including technology development, operations and business development to support flawless project execution and delivery management. Ensure laboratory compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Support root cause investigations, CAPA, OOS/OOT and non-conformance resolution related to design verification testing. Provide technical guidance and mentorship to junior engineers and laboratory staff. Participate in internal and external audits, including regulatory inspections. Maintain and improve quality systems, including CAPA, Nonconformances, calibration and maintenance and equipment qualification. Stay ahead of evolving regulatory expectations for combination products and contribute to continuous improvement initiatives. Data Review & Project Release Conduct timely reviews of project documentation including but not limited to protocol, laboratory data, audit trails, and reports prior to release to the client Quality Management System Execution and maintenance of QMS activities including: Provide problem solving and root cause analysis expertise to lead / support OOS/Deviation/CAPA investigations Review Test Method Validation and provide quality expertise in the development of test methods and protocols Act as technical QA representative during audits Compliance & Continuous Improvement Identify and drive implementation of improvements in current quality systems and processes. Achieves Key Performance Indicator (KPI) objectives by helping develop the appropriate production/quality data collection process, collecting data (including nonconformance, OOS, OOT, CAPAs, Deviations), and conducting the appropriate trending analysis to allow for the appropriate continuous improvement strategic plans to be enacted. Prepare and present quality reports and metrics to senior management Support ZebraSci QMS integration into BD Quality Global procedures and systems. Train and guide staff in quality procedures and compliance. Education and Experience Bachelor's or master's degree in engineering, Biomedical Sciences, or related field. Minimum 5 of experience in quality engineering, preferably in a combination product or medical device environment. Strong knowledge of design control, risk management (ISO 14971), and verification/validation principles. Demonstrated knowledge and experience in executing CAPA, with knowledge of investigation tools, problem solving process and methodology Experience with mechanical and analytical testing of drug-device combination products. Familiarity with 21 CFR Part 820, 21 CFR Part 4, and ISO 13485. Excellent analytical, organizational, and communication skills. Proficiency in statistical analysis tools and quality engineering methodologies (e.g., Gage R&R, DOE, FMEA). Experience with Laboratory Information Management Systems (LIMS) a plus. Experience managing or participating in audits a plus. Salary ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary offered to a successful candidate is based on experience, education, skills, and actual work location. Salary ranges may vary for Field-based and Remote roles. $80,600.00 - $133,000.00 USD Annual At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . Primary Work LocationUSA CA TemeculaAdditional LocationsWork Shift At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You. Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles. Salary Range Information $80,600.00 - $133,000.00 USD Annual

We are seeking a detail-oriented and driven Quality Engineer I to join our team. In this role, you will support quality assurance processes, drive continuous improvement initiatives, and ensure our products meet and exceed customer expectations. This is an exciting opportunity to make a meaningful impact and grow your career in quality engineering. Come join our growing team! Primary Duties & Responsibilities The Quality Engineer I: Performs moderately complex tasks to develop, apply, and maintain quality requirements for processing components and other materials into finished goods and products. Plans the quality measurements and controls on materials, processes, and product to provide adequate control of quality at minimum quality related costs. Analyzes quality information and feeds back analyses and recommendations for adjustment to product design, manufacturing process and equipment, and the quality system. Applies statistical methods to diagnose and correct improper quality practices, workmanship and process problems. On behalf of the Quality Manager, carries out essential steps in maintaining the company quality system. Quality Planning - 20% Recommends Quality objectives and goals in line with company Thrusts and Initiatives. Works with Quality Management, Marketing, Engineering and Customers in establishing specific quality requirements on individual products based upon customer requirements. Reviews contracts for manufacturing quality ability. Plans quality measurements and controls sufficient to provide adequate control of quality at minimum quality related costs. Applies and maintains Quality Standards for processing materials into partially finished or complete products. Assists Quality Management in determining and establishing the required quality procedures for controlling product quality. This planning includes the relative importance of quality characteristics and required quality levels; points in the flow for quality measurements to be made; methods and procedures for quality measurements by operators, inspectors, testers, and auditors; applicable Statistical Quality Control techniques; Quality Information feedback; required quality measurement and control equipment; and other pertinent quality procedures. Assures incorporation of applicable quality measurements into the manufacturing process and documentation. Defines and communicates quality requirements to Suppliers through Purchasing documents. Works with Manufacturing Engineering and Production to incorporate, where possible, the quality measurement and control devices with the production equipment to provide optimum mechanization and automation through integrated analysis and feedback of quality data. Promotes Continuous Improvement and Provides Customer Service - 10% Reviews product specifications and makes changes as necessary to assure a consistent product that meets or exceeds customer requirements. Appraises the nature of production quality problems, customer complaints and economical operations. Diagnoses chronic manufacturing quality problems. Identifies root causes, recommends and implements improvements and corrective/preventive actions. Analyzes, identifies basic causes, and feeds back analyses and recommendations regarding customer complaints. Participates with others in instigating corrective action. Follows-up and reports on corrective action progress to Quality Management. Performs failure analyses (FMEA), as needed, to reduce rejects and production problems. Acts as a primary interface with Government representatives (DCMAO) and customer source inspection personnel. Coordinates government and customer source inspections and Quality system surveys. Resolves issues with customers on warranty returns in a timely manner. Provides Support to Quality Control, Sales, Engineering, and Operations - 30% Reviews prints and quotes for QA requirements as necessary in a timely manner. Provides technical assistance to other departments. Maintains cognizance of customer and internal Engineering changes and procedural changes to assure accurate and up-to-date documentation is available to appropriate individuals at all times. Discusses quality issues and specifications with customer source and quality representatives as necessary. Provides assistance in the application of statistical methods to diagnose and correct improper quality practices, workmanship and process problems. Provides Production and Inspection areas all necessary interpretations of the quality requirements for inspection: their use, operation, and intent. Initiates and reviews Receiving Inspection and Test Records (RITR's). Writes Quality Assurance Instructions as required . Recommends and documents incoming inspection methods, in- process and final testing methods. Nonconforming Material Control - 40% Participates in the Material Review Board. Maintains segregation of nonconforming material. Processes Deviation Requests. Coordinates with Customers, Program Management and Sales to ensure that all products are acceptable before shipment. Processes Quality Improvement Requests, supplier deviation requests and waivers. Investigates nonconforming materials, components, and product for causes. Works closely with Quality Management, Production Control, Manufacturing, Engineering and Assembly for prompt and economic disposition and correction of the causes of nonconformities. Processes and codes NCMR's with applicable defect, cause and corrective action codes. Evaluates history for trends, etc. Education & Experience Minimum 2 years of related experience in one or more branches of Quality Assurance BS/MS in Quality Technology, Engineering, Mathematics, the Basic Sciences or equivalent degree. Skills Strong skills in inspection, writing, interpersonal communications Knowledge of Quality Assurance, Engineering, and Statistical Methods Good interpersonal skills and ability to work with challenging customers and suppliers Understanding Mil-Specs, ANSI, ISO etc. Skilled with interferometers, spectrophotometers, calipers, micrometers, Coordinate Measurement Machines, lasers and electronic test equipment American Society for Quality Certification as a Quality Engineer is a plus Lead auditor experience is a plus Working Conditions Lab and Office Environment Physical Requirements Standing. Particularly for sustained periods of time. 25% of the time. Walk. Occasionally move about inside the office to access file cabinets, office machinery, etc. Talking. Expressing or exchanging ideas by means of the spoken word. Those activities in which they must convey detailed or important spoken instructions to other employees accurately, loudly, or quickly. Hearing. Perceiving the nature of sounds at normal speaking levels with or without correction. Ability to receive detailed information through oral communication, and to make the discriminations in sound. Lifting. Raising objects from a lower to a higher position or moving objects horizontally from position-to-position. This factor is important if it occurs to a considerable degree and requires substantial use of upper extremities and back muscles. No more than 10 to 15 pounds. Safety Requirements All employees are required to follow the site EHS procedures and Coherent A&D EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent A&D: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent A&D is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. This role involves access to technology, materials, software, or hardware subject to U.S. export control laws. Therefore, to be considered, candidates must be classified as a “U.S. Person” under applicable regulations or be eligible for authorization under a U.S. government export license.

Program Quality Engineer, Armtec Defense Technologies Armtec Defense Technologies (Armtec) is an operating unit of the Transdigm Group (NYSE: TDG), an industry leader in aerospace and defense products and services. Armtec is comprised of three business units producing subcomponents for ordnance in Coachella, CA; decoy countermeasure flares in Camden AR; and radar countermeasure chaff in Lillington NC. At Armtec, we welcome skilled and enthusiastic people who share our determination and high standards to join us in our mission-critical work supporting the US and allied war-fighters who serve us all by defending democracy and protecting freedom. This position is staffed in Coachella, at Armtec's world-class, sole-source production facility for felted fiber nitrocellulose combustible cartridge cases for medium and large caliber military ammunition; and pyrophoric payloads for training grenades. Company Profile Company: Armtec Defense Technologies is an operating unit of the TransDigm Group (NYSE: TDG). Industry: Manufacturing Combustible Ordnance and Countermeasures Job Overview Title: Program Quality Engineer Job Family: Manufacturing Management Reports to: Site Leader Works with: mid-level managers, supervisors, engineers, and quality assurance; as well as significant direct interface with customers from U.S. Dept. of Defense and major prime contractors. Location: Coachella, California Type: Full-Time Job Summary The Program Quality Engineer at Armtec Defense Technologies is responsible for Quality function leadership on one or more strategic production programs. This responsibility includes both the management of daily production quality activities and personnel, but also requires supporting the strategic growth of the program by engaging with customers, developing and deploying processes around new products, and analyzing performance trends and results and driving fundamental quality process and performance improvements within the program. They are a peer with their Program, Operations, and Engineering Integrated Product Team Leaders, and must work in concert with this leadership team to ensure that our contractual commitments are met, and that Quality program objectives and metrics are achieved and are continually improved. On this team, the Program Quality Engineer is the main point of contact and authority within their assigned program for all Quality activities and decisions and ensures that required quality activities to support the program are identified, prioritized, and completed. Primary Responsibilities Identify, define, and coordinate key quality efforts that are needed to support their assigned program. Mentor and develop direct reports in quality processes and production methods and requirements. Coordinate and negotiate changes in quality requirements with our customers. Regularly collect and communicate status of technical activities within the program team, and to executive leadership as needed. Lead failure analysis investigations and perform root cause analysis on product quality and process issues to help expedite return to operation activities and ensure prevention of future problems. Perform DMAIC studies, and design/execute DoE's to identify driving factors that impact product characteristics and implement controls to improve process capability. Ensure our measurement systems are reliable and repeatable and always within calibration. Analyze production performance metrics and trends to identify key performance parameters and identify potential improvement and risk areas. Drive down scrap rates and improve product yields. Drive down product characteristic variability measures, improve process capabilities (Cpk/Ppk) Create product inspection plans and procedures, and design data capture and analysis systems to ensure real-time visibility of product compliance to specifications. Review and audit production procedures to ensure adequacy. Collect, monitor and improve data on Cost of Poor Quality, and provide a strategic vision for driving improvements in assigned program. Read, interpret, and evaluate contractual quality requirements and ensure requirement visibility and compliance. Review lot shipment paperwork as needed to ensure accuracy and completeness. Interface with internal and external customers on technical issues. Maintain the highest ethical standards, even when challenged from above Understand and live by Armtec's ethics and business conduct policies Education & Professional Work Experience Requirements Bachelor's degree, preferably in Engineering, Mathematics, Statistics, or Manufacturing. Prefer additional ASQ Certifications as a CQE, and/or Six Sigma Black Belt. Strong leadership and team facilitation skills 5+ years of quality experience in a production environment, including experience using and implementing statistical process controls. Demonstrated experience leading failure analyses and performing root cause analysis in a manufacturing environment. Familiarity with ISO9001:2015 requirements In-depth knowledge of quality functional activities, in addition to lean methods of process flow control. Strong analytical & problem-solving skills, and ability to use statistical tools and techniques. Excellent written and verbal communication and presentation skills required. Must be dependable, responsible, and detail oriented and have the ability to deal with people effectively. Requires self-direction and ability/willingness to prioritize and take initiative Must be authorized to work in the U.S. To conform to U.S. export control regulations, applicant should be eligible for any required authorization from the U.S. Government Armtec Competencies Armtec seeks leaders who demonstrate a positive outlook, sense of urgency, and exhibit constant professionalism. We want our leaders to achieve results, while being cool under pressure; approachable, respectful, and motivating to their team and their peers. Work Hours 4/10 workweek To Apply Please apply on-line on the Armtec Career Website, ********************* Equal Opportunity Employer including Disability/Protected Vet status. Salary Range: $93,878 - 129,606/Annual Benefits Medical Dental Vision Health Savings Account (HSA) with generous company contribution Flexible Spending Accounts (FSA - Medical & Dependent Care) Life and Accident Death and Dismemberment Insurance Disability Insurance Parent Leave Pay Employee Assistance Program (EAP) Vacation Sick Leave Holidays (8 paid holiday including holiday shutdown weeks in July and December) 401(k) matching Tuition Assistance

GARNEY CONSTRUCTION A Quality Control Manager position in Location is available at Garney Construction. Join our Garney team to manage and support project Quality Management Specialists, ensuring each project is successful. The Quality Control Manager is responsible for the implementation, management, and execution of Quality Management Programs for Federal contracting projects. WHAT YOU WILL BE DOING * Develop and implement project Quality Management Systems to ensure compliance with contract quality standards * Review project CPM schedule to anticipate and request timely submittals * Review project schedules and prepare Government meeting notices to support schedules * Conduct weekly Quality Control meetings * Perform/supervise quality inspections as needed by the project or Project Manager * Provide effective and efficient communication with the Federal Government personnel * Promote Garney's safety programs and procedures to promote a safe working environment WHAT WE ARE LOOKING FOR * 10 years of construction experience, 3 years being Construction Quality Manager experience * Bachelor's Degree in Engineering, Construction Management, or related field * Current USACOE Construction Quality Management for Contractors Certification * EM 385 40 hour and OSHA 30-hour certifications LET'S TALK THE PERKS! * Salary Range - $136,200-$154,300 * Employee Stock Ownership Plan (ESOP) * 401K Retirement plan * Health, dental, vision and life insurance * Flexible Spending Account (FSA) / Health Savings Account (HSA) * Long-term disability * Wellness program * Employee Assistance Plan * Holidays and PTO * Bonus program CONTACT US If you have questions about the position, please contact Patrick Duque at ************************ . Please include resumes, references, job lists, and any other relevant documentation. Garney Construction and its subsidiaries are committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Garney Construction is a background screening, drug-free workplace. Agency Disclaimer: All vendors must have a signed Garney Construction Agreement, authorized by the Executive Team, to receive payment for any placement. Verbal or written commitments made by anyone other than a member of the Executive Team will not be considered binding. Any unsolicited resumes sent to Garney Construction or submitted to employees outside of the Recruiting Team will be deemed the property of Garney Construction. In such cases, Garney Construction will not be obligated to pay any placement fees. THE BENEFITS OF WORKING AT GARNEY Free medical, prescription, dental, and vision plans ($0 premiums) Virtual doctor visits with no co-pay Shares of company stock at no cost starting your first day 401(k) plan with a 3.5% match Student loan resources Weekly paychecks Paid time off 8 paid holidays Health Savings Account (HSA) with a lump sum and matching contributions Free life insurance & disability policy Free access to healthcare coordinators Counseling sessions with mental health professionals at no cost Access to consultations with legal/financial professionals at no cost Free programs assisting with weight loss, maternity health, prescriptions for chronic conditions, and more 50% employee discount in the Garney apparel store BUILDING SUSTAINABLE FUTURES WITH THE WORLD'S MOST PRECIOUS RESOURCES-WATER AND PEOPLE. EEO - it's the law poster Right to work This organization participates in E-verify Nearest Major Market: Riverside Nearest Secondary Market: Los Angeles

This position shall have overall responsibility for the contractor's quality control management program to include maintaining and overseeing the quality control management program for entire contract. **Primary Job Functions:** + Administer quality control management program + Responsible for overall quality assurance program + Monitor and inspect all delivery orders for compliance + Maintain records of inspections and certifications + Prepare monthly reports depicting findings of quality inspections + Periodically review the quality control program to ensure compliance + Examine processes for preventative and corrective maintenance; make suggestions based on findings + Perform inspections and re-inspections to ensure problems have been resolved + Collect data for the DMLSS system including work orders and equipment history + Research safety and quality topics online + May prepare incident and accident reports + May be tasked with preparing training materials and conducting employee safety meetings + May manage the disposal of hazardous waste + May research and issue infection control and interim Life Safety permits + May train personnel on material control and equipment and tool management + Other duties as assigned **Education, Experience and Certification:** **Required: Associate degree** **Required: 5 years of experience in preparing and enforcing quality management programs (QMS) on similar size, scope and complexity.** **Preferred: OSHA certification** **Knowledge, Skills, and Abilities:** + Knowledge of OSHA safety regulations and PPE procedures + Ability to conduct accident investigations and safety inspections + Strong written and oral communication skills **Financial Responsibilities:** Determine if the role has the authority over budget or revenue. If so, you must describe in what manner in the description box. **Travel Requirements:** 10% **Disclaimer:** CBRE Government & Defense Services are thrilled at the opportunity for you to apply for one of our roles. The base salary range for this position is $55,000- $82,000. This position may also be eligible for a wide range of competitive benefits that can include but are not limited to medical, well-being, financial planning and short-term benefits. This description is not intended to be an "all inclusive" list of the accountabilities of the job described. Rather, it describes the general nature of the job. In addition, some aspects of this job may change over time, according to business needs, and these changes may not be recorded immediately. The requirements stated represent the minimum levels of knowledge, skills and/or abilities to qualify and satisfactorily perform this job. THIS DOCUMENT SHOULD NOT BE CONSTRUED AS CREATING A CONTRACT OF EMPLOYMENT BETWEEN CBRE GOVERNMENT & DEFENSE SERVICES AND ANY OF ITS EMPLOYEES OR OTHERWISE ALTERING AN EMPLOYEE'S AT WILL EMPLOYMENT RELATIONSHIP WITH CBRE GOVERNMENT & DEFENSE SERVICES. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (**************************** notice from the Department of Labor.

The Quality Engineer is a skilled professional who, with limited supervision from the Quality Assurance Manager, applies advanced principles of product and service quality evaluation and control. This role leverages a diverse body of knowledge and technologies, including but not limited to Probability, Statistical Quality Control, Design of Experiments, Metrology, Inspection and Test, Quality System Audits, Human Factors and Motivation, and Quality Information Systems, to ensure excellence in processes and deliverables. Primary Duties & Responsibilities The Quality Engineer has the responsibility for the action required to: * Assist the Quality Assurance Manager with development and operation of Quality Systems * Review proposed contracts, products and processes to avoid or eliminate unnecessary quality difficulties. * Plan the quality measurements and controls on materials, processes, and product that provides adequate control of quality at minimum quality related costs. * Determine that manufacturing processes have sufficient capability to meet quality requirements. * Analyze quality information and feedback analyses and recommendations for adjustment to product design, manufacturing processes, equipment, and the quality system. * Inspection of optical components and hardware * Provide leadership in the application of statistical methods to diagnose and correct improper quality practices, workmanship and process problems. * On behalf of the Quality Assurance Manager, carry out essential steps in establishing and maintaining the company quality system. Quality Planning - 40% * Recommends Quality objectives and goals in line with company Thrusts and Initiatives. * Works with Quality Management, Marketing, Engineering and Customers in establishing specific quality requirements on individual products based upon customer requirements. * Reviews proposed and new contracts as well as new designs for manufacturing quality ability. * Able to create AS9100 FAI's * Plans quality measurements and controls sufficient to provide adequate control of quality at minimum quality related costs. * Ensures QA has adequate metrology to support quality requirements of new processes. * Participates in establishing and defining quality, performance and workmanship standards that cover such items as cosmetic appearance, surface characteristics, color, noise, and vibration as well as company standards that will be followed in the absence of customer engineering specifications, e.g., electronics workmanship, scratch/dig requirements, cleaning and handling of optics. * Develops, applies, revises and maintains Quality Standards for processing materials into partially finished or complete products. * Assists Quality Management in determining and establishing the required quality procedures for controlling product quality. This planning includes the relative importance of quality characteristics and required quality levels; points in the flow for quality measurements to be made; methods and procedures for quality measurements by operators, inspectors, testers, and auditors; applicable Statistical Quality Control techniques; Quality Information feedback; required quality measurement and control equipment; and other pertinent quality procedures. * Assures incorporation of applicable quality measurements into the manufacturing process and documentation. * Provides Management with cost estimates and time schedules pertaining to the quality controls. * Periodically reviews quality planning to assure continued adequacy and effectiveness. * Defines and communicates quality requirements to Suppliers through Purchasing documents. * Provides management with cost estimates for quality-related labor and equipment. * Works with Manufacturing Engineering and Production to incorporate, where possible, the quality measurement and control devices with the production equipment to provide optimum mechanization and automation through integrated analysis and feedback of quality data. Promotes Continuous Improvement and Provides Customer Service - 30% * Analyzes quality information and recommends improvements that increase product and process uniformity, reliability and improve quality characteristics to reduce field failures and complaints. * Reviews product specifications and makes changes as necessary to assure a consistent product that meets or exceeds customer requirements. * Maintains awareness of new or better technologies for product metrology and evaluation. * Appraises continuing effectiveness of the quality system for quality levels, nature of production quality problems, customer complaints and economical operations. * Diagnoses chronic manufacturing quality problems. Identifies root causes, recommends and implements improvements and corrective/preventive actions. * Determines which product and process quality characteristics require process capability studies. * Fosters a quality-mindset throughout the company and in suppliers of purchased materials. * Analyzes, identifies basic causes, and feeds back analyses and recommendations regarding customer complaints. Participates with others in instigating corrective action. Follows-up and reports on corrective action progress to Quality Management. * Performs failure analyses (FMEA), as needed, to reduce rejects and production problems. * Acts as a primary interface with Government representatives (DCMAO) and customer source inspection personnel. Coordinates government and customer source inspections and Quality system surveys. * Maintains a favorable technical image for the Laser Power Corporation Quality Engineering group to the customers. * Resolves issues with customers on warranty returns in a timely manner. Provides Support to Quality Control, Sales, Engineering and Operations - 20% * Reviews prints and quotes for QA requirements as necessary in a timely manner. * Provides technical assistance to other departments. * Maintains cognizance of customer and internal Engineering changes and procedural changes to assure accurate and up-to-date documentation is available to appropriate individuals at all times. * Discusses quality issues and specifications with customer source and quality representatives as necessary. * Provides leadership in the application of statistical methods to diagnose and correct improper quality practices, workmanship and process problems. * Provides Production and Inspection areas all necessary interpretations of the quality requirements for inspection: their use, operation, and intent. * Visits key material blanks and component suppliers, as needed, to maintain a timely supply of quality products. * Initiates and reviews Receiving Inspection and Test Records (RITR's). * Writes Quality Assurance Instructions as required. * Develops and implements quality orientation programs for all personnel to ensure understanding of quality objectives, programs, plans, and techniques. * Provides quality training programs for personnel in Production operations as well as other areas. Recommends and documents incoming inspection methods, in-process and final testing methods. Nonconforming Material Control - 10% * Chairs the Material Review Board. Maintains segregation of nonconforming material. * Processes Deviation Requests. Coordinates with Customers, Program Management and Sales to ensure that all products are acceptable before shipment. * Processes Quality Improvement Requests, supplier deviation requests and waivers. * Investigates nonconforming materials, components, and product for causes. * Works closely with Quality Management, Production Control, Manufacturing, Engineering and Assembly for prompt and economic disposition and correction of the causes of nonconformities. * Processes and codes NCMR's with applicable defect, cause and corrective action codes. Evaluates history for trends, etc. Education & Experience * Minimum 7 years of experience in one or more branches of Quality Assurance * BS/MS in Quality Technology, Engineering, Mathematics, the Basic Sciences or equivalent degree. Skills * Strong skills in inspection, writing, interpersonal communications * Knowledge of Quality Assurance, Engineering, and Statistical Methods * Good interpersonal skills and ability to work with challenging customers and suppliers * Understanding Mil-Specs, ANSI, ISO etc. * Skilled with interferometers, spectrophotometers, calipers, micrometers, Coordinate Measurement Machines, lasers and electronic test equipment * American Society for Quality Certification as a Quality Engineer is a plus * Lead auditor experience is a plus Working Conditions * Lab and Office Environment Physical Requirements * Standing. Particularly for sustained periods of time. 25% of the time. * Walk. Occasionally move about inside the office to access file cabinets, office machinery, etc. * Talking. Expressing or exchanging ideas by means of the spoken word. Those activities in which they must convey detailed or important spoken instructions to other employees accurately, loudly, or quickly. * Hearing. Perceiving the nature of sounds at normal speaking levels with or without correction. Ability to receive detailed information through oral communication, and to make the discriminations in sound. * Lifting. Raising objects from a lower to a higher position or moving objects horizontally from position-to-position. This factor is important if it occurs to a considerable degree and requires substantial use of upper extremities and back muscles. No more than 10 to 15 pounds. Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. To conform to U.S. Government export regulations (ITAR), applicant must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8. U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State."

Primary contact for engineering support of In-Process Inspectors. Support production efforts and process improvements (trend analysis, process validation, SPC). Coordinate In-Process MRB acitvities. Support Quality Systems (perform audits, SOP improvement, training, CAPA investigations). Ensure from the Quality prospective the transfer of new products from R&D to Production. Support Statistical Techniques and SPC interpretation. Present PPR and Management Review. 0-1 years of industry experience in ISO-9001 environment, preferably medical device. Bachelor of Science or higher degree in ME, IE or equivalent. This position will be a line support engineer. QualificationsEnter qualifications here Additional Information

The Lab Services Quality Engineer is responsible for ensuring quality by design, ensuring that method development and execution is always conducted in compliance with laboratory quality and compliance standards. S(he) supports technical data review and ensures data and documentation generated meet cGMP requirements. The Lab services Quality Engineer closely collaborates with Technology Development and Operations functions and acts as the technical lead within QA department to work with engineering on review of engineering drawings, data analysis, reporting and investigations S(he) ensures the maintenance and enhancement of the company's Quality Management System (QMS), with a focus on continuous improvement and operational excellence. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Key Responsibilities: * Lead and implement design verification testing activities for combination products in accordance with FDA 21 CFR part 210,211, 820, ISO/IEC 17025 and ISO 13485 * Develop and review test protocols, methods, and reports to ensure compliance with design control and risk management requirements. * Collaborate with cross-functional teams including technology development, operations and business development to support flawless project execution and delivery management. * Ensure laboratory compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). * Support root cause investigations, CAPA, OOS/OOT and non-conformance resolution related to design verification testing. * Provide technical guidance and mentorship to junior engineers and laboratory staff. * Participate in internal and external audits, including regulatory inspections. * Maintain and improve quality systems, including CAPA, Nonconformances, calibration and maintenance and equipment qualification. * Stay ahead of evolving regulatory expectations for combination products and contribute to continuous improvement initiatives. Data Review & Project Release * Conduct timely reviews of project documentation including but not limited to protocol, laboratory data, audit trails, and reports prior to release to the client * Quality Management System Execution and maintenance of QMS activities including: * Provide problem solving and root cause analysis expertise to lead / support OOS/Deviation/CAPA investigations * Review Test Method Validation and provide quality expertise in the development of test methods and protocols * Act as technical QA representative during audits * Compliance & Continuous Improvement * Identify and drive implementation of improvements in current quality systems and processes. * Achieves Key Performance Indicator (KPI) objectives by helping develop the appropriate production/quality data collection process, collecting data (including nonconformance, OOS, OOT, CAPAs, Deviations), and conducting the appropriate trending analysis to allow for the appropriate continuous improvement strategic plans to be enacted. * Prepare and present quality reports and metrics to senior management * Support ZebraSci QMS integration into BD Quality Global procedures and systems. * Train and guide staff in quality procedures and compliance. Education and Experience * Bachelor's or master's degree in engineering, Biomedical Sciences, or related field. * Minimum 5 of experience in quality engineering, preferably in a combination product or medical device environment. * Strong knowledge of design control, risk management (ISO 14971), and verification/validation principles. * Demonstrated knowledge and experience in executing CAPA, with knowledge of investigation tools, problem solving process and methodology * Experience with mechanical and analytical testing of drug-device combination products. * Familiarity with 21 CFR Part 820, 21 CFR Part 4, and ISO 13485. * Excellent analytical, organizational, and communication skills. * Proficiency in statistical analysis tools and quality engineering methodologies (e.g., Gage R&R, DOE, FMEA). * Experience with Laboratory Information Management Systems (LIMS) a plus. * Experience managing or participating in audits a plus. Salary ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary offered to a successful candidate is based on experience, education, skills, and actual work location. Salary ranges may vary for Field-based and Remote roles. $80,600.00 - $133,000.00 USD Annual At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . Primary Work Location USA CA Temecula Additional Locations Work Shift At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You. Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles. Salary Range Information $80,600.00 - $133,000.00 USD Annual

The Quality Engineer is a skilled professional who, with limited supervision from the Quality Assurance Manager, applies advanced principles of product and service quality evaluation and control. This role leverages a diverse body of knowledge and technologies, including but not limited to Probability, Statistical Quality Control, Design of Experiments, Metrology, Inspection and Test, Quality System Audits, Human Factors and Motivation, and Quality Information Systems, to ensure excellence in processes and deliverables. Primary Duties & Responsibilities The Quality Engineer has the responsibility for the action required to: Assist the Quality Assurance Manager with development and operation of Quality Systems Review proposed contracts, products and processes to avoid or eliminate unnecessary quality difficulties. Plan the quality measurements and controls on materials, processes, and product that provides adequate control of quality at minimum quality related costs. Determine that manufacturing processes have sufficient capability to meet quality requirements. Analyze quality information and feedback analyses and recommendations for adjustment to product design, manufacturing processes, equipment, and the quality system. Inspection of optical components and hardware Provide leadership in the application of statistical methods to diagnose and correct improper quality practices, workmanship and process problems. On behalf of the Quality Assurance Manager, carry out essential steps in establishing and maintaining the company quality system. Quality Planning - 40% Recommends Quality objectives and goals in line with company Thrusts and Initiatives. Works with Quality Management, Marketing, Engineering and Customers in establishing specific quality requirements on individual products based upon customer requirements. Reviews proposed and new contracts as well as new designs for manufacturing quality ability. Able to create AS9100 FAI's Plans quality measurements and controls sufficient to provide adequate control of quality at minimum quality related costs. Ensures QA has adequate metrology to support quality requirements of new processes. Participates in establishing and defining quality, performance and workmanship standards that cover such items as cosmetic appearance, surface characteristics, color, noise, and vibration as well as company standards that will be followed in the absence of customer engineering specifications, e.g., electronics workmanship, scratch/dig requirements, cleaning and handling of optics. Develops, applies, revises and maintains Quality Standards for processing materials into partially finished or complete products. Assists Quality Management in determining and establishing the required quality procedures for controlling product quality. This planning includes the relative importance of quality characteristics and required quality levels; points in the flow for quality measurements to be made; methods and procedures for quality measurements by operators, inspectors, testers, and auditors; applicable Statistical Quality Control techniques; Quality Information feedback; required quality measurement and control equipment; and other pertinent quality procedures. Assures incorporation of applicable quality measurements into the manufacturing process and documentation. Provides Management with cost estimates and time schedules pertaining to the quality controls. Periodically reviews quality planning to assure continued adequacy and effectiveness. Defines and communicates quality requirements to Suppliers through Purchasing documents. Provides management with cost estimates for quality-related labor and equipment. Works with Manufacturing Engineering and Production to incorporate, where possible, the quality measurement and control devices with the production equipment to provide optimum mechanization and automation through integrated analysis and feedback of quality data. Promotes Continuous Improvement and Provides Customer Service - 30% Analyzes quality information and recommends improvements that increase product and process uniformity, reliability and improve quality characteristics to reduce field failures and complaints. Reviews product specifications and makes changes as necessary to assure a consistent product that meets or exceeds customer requirements. Maintains awareness of new or better technologies for product metrology and evaluation. Appraises continuing effectiveness of the quality system for quality levels, nature of production quality problems, customer complaints and economical operations. Diagnoses chronic manufacturing quality problems. Identifies root causes, recommends and implements improvements and corrective/preventive actions. Determines which product and process quality characteristics require process capability studies. Fosters a quality-mindset throughout the company and in suppliers of purchased materials. Analyzes, identifies basic causes, and feeds back analyses and recommendations regarding customer complaints. Participates with others in instigating corrective action. Follows-up and reports on corrective action progress to Quality Management. Performs failure analyses (FMEA), as needed, to reduce rejects and production problems. Acts as a primary interface with Government representatives (DCMAO) and customer source inspection personnel. Coordinates government and customer source inspections and Quality system surveys. Maintains a favorable technical image for the Laser Power Corporation Quality Engineering group to the customers. Resolves issues with customers on warranty returns in a timely manner. Provides Support to Quality Control, Sales, Engineering and Operations - 20% Reviews prints and quotes for QA requirements as necessary in a timely manner. Provides technical assistance to other departments. Maintains cognizance of customer and internal Engineering changes and procedural changes to assure accurate and up-to-date documentation is available to appropriate individuals at all times. Discusses quality issues and specifications with customer source and quality representatives as necessary. Provides leadership in the application of statistical methods to diagnose and correct improper quality practices, workmanship and process problems. Provides Production and Inspection areas all necessary interpretations of the quality requirements for inspection: their use, operation, and intent. Visits key material blanks and component suppliers, as needed, to maintain a timely supply of quality products. Initiates and reviews Receiving Inspection and Test Records (RITR's). Writes Quality Assurance Instructions as required. Develops and implements quality orientation programs for all personnel to ensure understanding of quality objectives, programs, plans, and techniques. Provides quality training programs for personnel in Production operations as well as other areas. Recommends and documents incoming inspection methods, in-process and final testing methods. Nonconforming Material Control - 10% Chairs the Material Review Board. Maintains segregation of nonconforming material. Processes Deviation Requests. Coordinates with Customers, Program Management and Sales to ensure that all products are acceptable before shipment. Processes Quality Improvement Requests, supplier deviation requests and waivers. Investigates nonconforming materials, components, and product for causes. Works closely with Quality Management, Production Control, Manufacturing, Engineering and Assembly for prompt and economic disposition and correction of the causes of nonconformities. Processes and codes NCMR's with applicable defect, cause and corrective action codes. Evaluates history for trends, etc. Education & Experience Minimum 7 years of experience in one or more branches of Quality Assurance BS/MS in Quality Technology, Engineering, Mathematics, the Basic Sciences or equivalent degree. Skills Strong skills in inspection, writing, interpersonal communications Knowledge of Quality Assurance, Engineering, and Statistical Methods Good interpersonal skills and ability to work with challenging customers and suppliers Understanding Mil-Specs, ANSI, ISO etc. Skilled with interferometers, spectrophotometers, calipers, micrometers, Coordinate Measurement Machines, lasers and electronic test equipment American Society for Quality Certification as a Quality Engineer is a plus Lead auditor experience is a plus Working Conditions Lab and Office Environment Physical Requirements Standing. Particularly for sustained periods of time. 25% of the time. Walk. Occasionally move about inside the office to access file cabinets, office machinery, etc. Talking. Expressing or exchanging ideas by means of the spoken word. Those activities in which they must convey detailed or important spoken instructions to other employees accurately, loudly, or quickly. Hearing. Perceiving the nature of sounds at normal speaking levels with or without correction. Ability to receive detailed information through oral communication, and to make the discriminations in sound. Lifting. Raising objects from a lower to a higher position or moving objects horizontally from position-to-position. This factor is important if it occurs to a considerable degree and requires substantial use of upper extremities and back muscles. No more than 10 to 15 pounds. Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. To conform to U.S. Government export regulations (ITAR), applicant must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8. U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State."

Quality Engineer, Armtec Defense Technologies Armtec Defense Technologies (Armtec) is an operating unit of the Transdigm Group (NYSE: TDG), an industry leader in aerospace and defense products and services. Armtec is comprised of three business units producing subcomponents for ordnance in Coachella, CA; decoy countermeasure flares in Camden AR; and radar countermeasure chaff in Lillington NC. At Armtec, we welcome skilled and enthusiastic people who share our determination and high standards to join us in our mission-critical work supporting the US and allied war-fighters who serve us all by defending democracy and protecting freedom. This position is staffed in Coachella, at Armtec's world-class, sole-source production facility for felted fiber nitrocellulose combustible cartridge cases for medium and large caliber military ammunition; and pyrophoric payloads for training grenades. Company Profile Company: Armtec Defense Technologies is an operating unit of the TransDigm Group (NYSE: TDG). Industry: Manufacturing Combustible Ordnance and Countermeasures Job Overview Title: Quality Engineer Job Family: Quality Engineers Reports to: Site Leader Works with: mid-level managers and supervisors, employees Location: Coachella, California Type: Full-Time Job Summary The Quality Engineer is part of an internal Integrated Product Team (IPT) of manufacturing, engineering, Program Management, and support staff (Maintenance, Purchasing, etc.). The Quality Engineer participates in all ares of Armtec's Quality Management System QMS) and provides systems support for the various quality functions including contract and purchase order review, interpretation of contractual quality requirements and plans for compliance, data collection and analysis, and preparation of quality management system documentation. The Quality Engineer designs and manages process improvement projects as team leader and facilitator, and they support Armtec's continual improvement efforts including ISO 9001:2008, internal audits Lean Six Sigma, and Statistical Process Control (SPC). Primary Responsibilities Customer point of contact for all quality topics for assigned programs. Maintain excellent customer relations. Manages and supervises direct report quality inspectors for assigned programs. Applies systematic problem solving and improvement concepts in a team environment to resolve product quality issues. Prepares test plans for conducting experimental trials and qualification of tooling to support improvement efforts, including any required Management of Change (MOC) documentation, work instructions, maintenance work orders and subsequent Capital Expense Requests (CERs). Analyzes cost of quality and performance data to plan and deploy improvement efforts. Provide routine, accurate reports to senior management and program team members, as required. Reads and understands customer requirements, product drawings and specifications and provide written interpretation for performance. Understands, is able to generate, and oversees the timely completion of quality documentation required for the approval of production deliveries. Participates in all areas of Armtec's quality management system. Provides input in areas not specific to quality assurance but essential to Armtec's Shared Values and team based management structure. Maintains the highest ethical standards, even when challenged from above. Understands and lives by Armtec's ethics and business conduct policies. Qualifications Bachelor of Science degree, preferably in Engineering, Mathematics, Statistics, or Manufacturing. One to five years experience in Quality Engineering or comparable work experience. Knowledge of Government specifications, contracts, and ISO 9001:2008 requirements. Knowledge of management systems for improving quality, i.e. benchmarking, project management, six-sigma, experimental design. Knowledge of Lean Manufacturing tools and Statistical Process Control (SPC). Must be dependable, responsible, and accurate and have the ability to deal with people effectively. Armtec Competencies Armtec seeks leaders who demonstrate a positive outlook; sense of urgency, professionalism; cool under pressure; approachability, charismatic leadership, interpersonal savvy, motivational skills, conflict management, assessing people, organizing, planning, priority setting, building effective teams, managerial courage, fairness to direct reports and relentless drive for results. Education & Professional Work Experience Requirements Must be authorized to work in the U.S. To conform to U.S. export control regulations, applicant should be eligible for any required authorization from the U.S. Government Work Hours & Travel 4/10 workweek with some overtime on Fridays or weekends as necessary, to meet program objectives. Some US travel may be required, normally a few multi-day trips per year. To Apply Please apply on-line on the Armtec Career Website, ********************* Equal Opportunity Employer, including disability and protected veterans status. Salary Range: $75,275 - $115,000/Annual Benefits Medical Dental Vision Health Savings Account (HSA) with generous company contribution Flexible Spending Accounts (FSA - Medical & Dependent Care) Life and Accident Death and Dismemberment Insurance Disability Insurance Parent Leave Pay Employee Assistance Program (EAP) Vacation Sick Leave Holidays (8 paid holiday including holiday shutdown weeks in July and December) 401(k) matching Tuition Assistance