Airbus is the largest aeronautics and space company in Europe and a worldwide leader. Airbus has built on its strong European heritage to become truly international - with roughly 180 locations and 12,000 direct suppliers globally. The company has aircraft and helicopter final assembly lines across Asia, Europe and the Americas, and has achieved a more than sixfold order book increase since 2000.
Position Summary: The Supply Chain Quality Manager (SCQM) will be part of an international community, responsible for a portfolio of suppliers / vendors, ensuring supplier performance; capacity; de-risking and development needs are secured to meet the evolving business requirements. Training
and development will be provided to ensure the required skills and competences are attained, aligned with the company's methods and processes. In conjunction, a robust induction training plan will be developed to ensure training of product, methods, tools etc.
are sequenced in a robust way. This position is based in Los Angeles, CA with travel to supplier sites. Primary Responsibilities: Work onsite at either the allocated supplier site or in an Airbus office minimum 3 days a week and will be required to be collocated to the Supplier Center of Gravity. Ensure maturity and robustness of Supplier's manufacturing and supply chain processes to avoid supply failures Drive continuous improvement
of Supply Chain related performances for deliveries of supplied products Review supplier capacity and capability to secure ramp-up period as well as Airbus industrial objectives (major planning changes, ramp down, etc.
) Monitor and analyze performance through Key Performance Indicators and organizing the surveillance of the suppliers through audits, backssments, recovery plan and mission, CID (Corrective, Improvement, Development) and industrial risks management with internal and external concerned parties Initiate and organize supplier's ramp-up capacity and capabilities backssments in order to secure ramp-up or major planning changes Monitor major industrial risks, major changes (industrial transfers, major planning changes) and supporting design changes on an industrial point of view in order to protect Airbus operations Initiate and follow recovery plans with Suppliers in case of delivery performances degradation to ensure deliveries are back to Airbus requirements Manage Suppliers' preventive/corrective action plans so achievements are at the expected level in terms of end results.
Prepare and support regular management reviews (PRM, Industrial Senior Management Meeting, and Quality Supply Chain Meetings) with suppliers to review regularly delivery and supply chain performances and ensuring that preventive/corrective & improvement actions are continuously undertaken.
Manage relationships with internal stakeholders, such as MFT leaders, Programs and FALs (communication, customer / supplier relation & meetings, improvement actions). Qualified Experience / Skills / Training: Education: Required: Bachelor's Degree in Engineering/Industrial Engineering or similar or equivalent combination of education and/or experience Experience: Required: Minimum of 3 years professional experience in a procurement operations environment (monitoring and auditing suppliers) Previous Aerospace experience highly preferred Licensure/Certifications: Preferred: Green Belt/Black Belt certification, CPIM certification (Certified in Production & Inventory Management) Knowledge, Skills, Demonstrated Capabilities: Required: Knowledge of Supply Chain and Quality Processes Preferred: Knowledge of Quality Regulations, Quality Core Tools Knowledge, Practical Problem Solving, International Mgmt.
system standards, Authorities / Regulations / Standards, Knowledge of QMS, Auditing backssing, IPCA+ and CCP tools Communication Skills (Spoken, Written, Influencing, Proficiency in Other Languages): English (Reading - Speaking - Writing: Fluent/Negotiation) Communicating at all levels within the supplier's organization and Airbus to influence the decision making Ability to summarize complex industrial situations in a clear manner Team Player with excellent communication skills, customer-oriented, problem solving and flexible way of working.
Technical Systems Proficiency: Microsoft Office Google Suite proficiency highly preferred Travel Required: 60% Domestic and International Valid Driver's License required Citizenship: Authorization to work in the U.
S. is required. Decision Making, Complexity: The Job holder will be part of a team and will be able to act autonomously and but operationally driven by the Procurement commodity in Europe. The management support for the Job Holder is US based, as are the suppliers. Most internal customers will be based in Europe. Organizational information: The job holder will be part of the Airbus Americas Procurement team whose internal customer is the Procurement Operations organization in Europe primarily and all Airbus Final Assembly Lines (FALs). Nature of Contacts: Involved, negotiation type Communication on a daily basis with internal and external parties Physical Requirements: The job content requires the ability to travel via car and airplane.
Equal Opportunity: Airbus is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, interactionual orientation, national origin, genetics, disability, age, or veteran status. Airbus is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
As a leader in our field, Airbus provides relocation assistance for qualified positions and a comprehensive compensation and benefits package. As a matter of policy, Airbus does not sponsor visas for US positions unless specified. Only applicants with current work authorization will be considered. Airbus does not offer tenured or guaranteed employment. Employment with Airbus is at will, meaning either the company or the employee can terminate the employment relationship at any time, with or without cause, with or without notice. Job Posted by Applicant Pro
Optimization, Learning and Insights. We focus on helping our clients generate more value for their customers. With over 5,000 employees based in more than 80 countries worldwide, our teams provide industry-leading expertise. We have combined our deep industry expertise with cutting-edge technology solutions to help our automotive clients increase revenue and reduce costs, while enhancing operational efficiency and improving customer satisfaction.
Our goal is to help our customers reach their full potential and to excel as their global partner of choice. Summary MSX International is seeking qualified candidates responsible for reviewing campaign claims for compliance with our client’s
policies and procedures. Day to Day Responsibilities Review previously adjudicated claims for accuracy Understand complex warranty policies used to adjudicate manufacturer claims.
Work to a timescale, completed a set number of audits in a given timeframe Demonstrate a sound understanding of manufacturer warranty policy What you bring Minimum 2 years of experience in a project management role. 2 years of experience performing general office duties. 1 year of experience in an automotive-related field. 1 year of experience in an Auditing position Excellent oral and written communication skills. Excellent problem-solving skills Ability to apply Deductive and Inductive reasoning to produce
logical conclusions & improvements to processes Must be legal to work in the United States MSX International is an Equal Employment Opportunity Employer committed to employing a diverse workforce.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, interactionual orientation, gender identity, disability and protected veteran status, age, or any other characteristic protected by law. The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, and other business and organizational needs.
The disclosed range estimate may not have been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At MSXi, it is not typical for an individual to be hired at the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $28 to $30 hourly based on current experience. Apply NOW! #MSXNAJobs
The company partners with clinicians to develop innovative technologies that improve the quality of care for arrhythmia patients worldwide. For more information, visit The Senior Quality Engineer - plans, coordinates and executes quality assurance activities intended to ensure effective product quality processes are in place and executed throughout lifecycle of product.
Involved in New Product Development (NPD) teams and other activities to develop products, design verification tests, process validations and quality processes to ensure compliance with the company's Quality System policies and procedures and applicable external requirements and standards. As needed, assists to develop
quality-engineered systems and products, and support qualification and validation activities. Will be considered a subject matter expert (SME) on Quality matters, relevant Quality tools and will work on complex problems and projects.
Will show leadership in driving program/projects and innovating compliant approaches and solutions to problems. Shares technical expertise with others and develop other engineers. A few of the responsibilities may involve collaborating with other members of the Design Team. Will contribute to activities including risk management document development, creation, and design of catheter test methods, authoring of test protocols, and testing of products during
their development cycle. If you are and individual who enjoys working with the other team members and changing the lives of our patients around the world come join our team at Biosense Webster!
Key Responsibilities: Under limited supervision and general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: This position will support day-to-day responsibilities of maintaining the Risk Management System in accordance with ISO14971 and all Corporate, MD and CSS Standards. The position will be responsible for the ongoing maintenance of the Risk Management files for all current marketed product in accordance with all applicable requirements.
Reviews and continuously leads efforts to improve the Risk Management System at BWI Maintains dashboards and other reports of performance metrics as required. Provides regular updates and status reports to management. Initiates Company issue escalation process as required. Working with other functional groups, including R&D and Operations in support of new product development, engineering projects, quality assurance activities, and lifecycle management. Applying Quality Engineering tools/processes in development and implementation of practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle.
Remains informed of new or revised regulations and/or guidelines and backsses impact on company Risk Management processes. Supports internal and external audits Develop and establish effective quality control and support associated risk management plans, AFMEA, DFMEA and PFMEA. Review and/or approve process and product validation protocols and reports, equipment qualifications, engineering change orders. Ensure that development activities follow design control requirements (Design Trace Matrix), product is tested per applicable standards, GSPR are met per the MDR, and product is properly transferred to manufacturing per applicable specifications.
Technical problem solving, failure analysis, and root cause determination. Makes decisions independently on engineering problems and methods and represents the organization in conferences to resolve important questions and to plan and coordinate work. Recommend issue resolution to management for significant capability and compliance issues. Works closely with functional leadership in planning and completing project milestones.
Plans, develops, coordinates, and directs one or more large important engineering projects or a number of small projects with many complex features. Carries out complex or novel assignments requiring the development of new or improved techniques or procedures. backsses the feasibility and soundness of proposed engineering evaluation tests, products or equipment when necessary, data are insufficient or confirmation by testing is advisable. Responsible for communicating business related issues or opportunities to next management levels.
Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures Performs other duties assigned as needed Required: Bachelor's degree, required; preferably in engineering and/or scientific field. A minimum of 4 years of quality, manufacturing, or research and development experience in a medical device or other regulated industry Ability to define problems, collect and analyze data, establish facts, and draw conclusions and recommendations Critical thinking and investigation skills Ability to multitask, including ability to understand customer requirements, retrieve relevant information, and provide responses satisfactorily and with immediacy Ability to function in a team environment and deliver on team objectives Ability to effectively collaborate and communicate with internal and external partners at all levels of the organization including influencing and negotiating resulting in positive business and quality outcomes.
Preferred: Ability to use broad knowledge of regulatory, technical, and business requirements to conduct due diligence backssments Ability to apply project management skills to ensure fulfillment of new product development requirements Ability to develop and implement Quality standards.
Demonstrated auditing and problem-solving skills Six Sigma/ Design for Six Sigma experience, and/or knowledge of Process Excellence tools Lean manufacturing experience Knowledge of Quality and operations systems and processes, including GMP Familiar with general quality management system concepts, including good documentation practice (GDP), corrective and preventive action (CAPA), and document change control practices. Ability to function in a team environment and deliver on team objectives is required.
Professional demeanor on the phone and in email is required. Strong attention to detail is required. Prior medical device complaint handling experience, or knowledge of medical device regulations is required. Project management and/or process mapping experience. Strong written and verbal communication skills are required. Developed presentation skills. Other: This position is located in Irvine, California and will require up to 20% travel domestic and international. The anticipated base pay range for this position is $76,000 to $121,000. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.
smart, driven people in a room together, they will accomplish great things. We maintain a supportive culture that celebrates continuous learning, diverse perspectives, and sharing the wins. That's why we have our eyes on you. About The Role Tevora is seeking a Senior QA Engineer to assist in the daily functions and processes of the Dev Ops team.
As a Sr. QA Engineer, you will play a vital role in ensuring the quality, reliability, and usability of our commercial software product. You will lead the QA efforts, collaborating closely with the development team, product manager, and other stakeholders to define and implement effective testing strategies. Your expertise in QA methodologies,
test automation, and the technology stack (Node. js, React, Type Script, Mongo DB, Postgre SQL, AWS) will be crucial in driving the quality assurance process and maintaining a high standard of product excellence.
Essential Functions: Collaborate with the product manager and development team to understand business requirements and define test strategies, test plans, and test cases. Design, develop, and maintain automated test scripts using Cypress, ensuring maximum test coverage and reliability. Conduct functional, regression, integration, and performance testing of software applications to identify defects and ensure adherence to quality standards. Implement and enhance test automation
frameworks, tools, and processes to improve efficiency and effectiveness of QA activities.
Collaborate with the development team to ensure that testable and reliable code is delivered, promoting test-driven development and continuous integration. Identify, document, and track software defects, working closely with the development team to facilitate their resolution and ensure timely delivery of high-quality software. Monitor and analyze test results, metrics, and quality trends to identify areas for improvement and recommend corrective actions. Establish and enforce quality assurance best practices, standards, and processes throughout the software development lifecycle.
Collaborate with cross-functional teams to ensure that QA activities align with project timelines and deliverables. Stay up-to-date with industry trends, advancements in QA methodologies, and emerging technologies to drive continuous improvement in the QA process. Additional duties as assigned. Qualifications: Proven experience as a QA Lead or similar role, with a strong background in software quality assurance methodologies, tools, and practices. Bachelors degree required or 5+ years experience in Software QA and Automation. Solid understanding of the technology stack, including Node.
js, React, Type Script, Mongo DB, and AWS infrastructure. Extensive experience in designing, implementing, and maintaining automated test scripts using Cypress or similar testing frameworks. Proficiency in test management and defect tracking tools, such as Jira, Test Rail, or similar. Strong knowledge of QA methodologies, test planning, test case design, and execution in Agile/Scrum environments. Familiarity with CI/CD pipelines and their integration with test automation frameworks. Excellent analytical and problem-solving skills, with a keen attention to detail and the ability to troubleshoot complex issues.
Strong leadership and communication skills, with the ability to collaborate effectively with cross-functional teams and stakeholders. Experience in performance testing and familiarity with related tools like JMeter or Gatling is a plus. ISTQB or similar certifications in software testing are advantageous. Continuous learning mindset and a passion for staying up-to-date with industry trends and emerging technologies in QA and test automation. Additional Qualifications: Valid driver's license as driving will be required in this role Ability to work a hybrid schedule (3 days) at our Irvine, CA office.
Eligible to work in the United States Benefits: Comprehensive Healthcare Benefits 401k w/ Employer Matching Hybrid Schedule Paid Vacations Paid Holiday Vibrant Work Culture Tevora is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, pregnancy, interactionual orientation, gender identity, national origin, age, protected veteran status, or disability status. Job Posted by Applicant Pro
