quality engineer resume sample pdf

Drug/Device Combination product experience would be beneficial, Ability to take initiative and to organize and prioritize own work is essential, Move OKL from a 2-week release cycle to one that can be as frequent as daily, Work with development and product teams to set release schedules and environments in a dynamic fast-paced environment, Help define best practices for source control, continuous integration, automated testing, build automation, deployment, and release management for our ERP system, Bridge the gap between manual testing and automation for our ERP system, Bachelor’s degree in computing science or related field, Knowledge of SQL and querying of databases required. There are plenty of opportunities to land a Supplier Quality Engineer job position, but it won’t just be handed to you. Prepare gage quote package and review received quotes. MBA desired, not required, Outstanding problem solving and conflict resolution skills. The noise level in the work environment is usually moderate. Create your resume now . Only a professionally well-written resume can help you land an engineering job. FDA, IMB, Notified bodies, etc), Maintain structured communication channels with strategic sourcing, identifying responsibility by commodity / supplier, Liaising with the Manufacturing and Quality groups, in assessing and addressing material quality issues with assigned suppliers, Maintenance of the Approved Supplier List (ASL) in conjunction with the Global Sourcing, Supplier Controls and Audit functions, Deliver continuous improvement activities focusing on supplier quality, Participate in supplier audit program - planning, execution and closure, Participate in supplier reviews for assigned suppliers as required, Partner with SQM functions and Strategic Sourcing on the developments and approval quality assurance agreements with suppliers, Good knowledge of continuous improvement methodologies, Plan, coordinate, and execute Quality Assurance requirements on investigation COQP top drivers, Assist/interact across the organization with Repair Order Administration (ROA), Operations, Materials, and Customer day-to-day quality issues, Manage the Quality Clinic and ACE QCPC process ensuring RRCA and mistake proofing is robust, Assist the Quality Manager and inspectors in establishing, implementing, and enforcing customer and regulatory quality requirements through AS9110 internal and external (supplier) auditing, Participate in quality improvement projects and assuring coordination with other functions or value streams objectives, Provide technical support and maintain a strong working relationship with the UTAS/PWC/PW and Embraer teams, Serve as an on-site customer interface for P&W at the Embraer and facility, Establish and maintain customer relations and other relevant functions, with respect to the quality for the PW1900G program as appropriate for the entire propulsion system, Graduate in a science, engineering or related background, Minimum 5 years in a QA Engineering / QE role, working within a recognised quality system within IVD, Medical Device or Pharma industry, Minimum 3 years validation experience in equipment/process/software is highly desirable, A working knowledge of regulatory requirements, A technical background or knowledge of IVD products or Medical devices would be advantageous, Awareness of statistical techniques and validation, Experience of internal, third party regulatory & external customer audits, The ideal candidate should demonstrate a logical and planned approach to all tasks, Excellent written, oral and communication skills, Be a team player and have high personal confidence, ability to liaise with other business divisions, The ability to work in a multi-disciplinary team environment, Be flexible and willing to carry out overtime as necessary when required, Be conscious of Health & Safety requirements at all times, Quality System Specialist for current and future programs. Manage agency visits within assigned product lines, Partner with buyers and suppliers to drive continuous improvements in supplier product performance (quality and delivery). Ensure corrective/preventative actions are implemented, verified, and communicated appropriately. Continue reading on to learn more about engineering resumes. defect vs. crash), Prepare reports summarizing manufacturing-related failure modes of warranty parts from top 5 composites suppliers, Organize a regular process of returning defective parts to these suppliers – coordinate global markets to ship samples, Develop and maintain a clear database summarizing shipments and analysis results on the supplier end – compare supplier and internal analysis reports for consistency, Investigation and Corrective Action Support, Serve as a technical resource to the quality team investigating field failure issues – help identify root causes related to both design and manufacturing, Recommend corrective actions based on returned component analysis/findings, Field Action Coordination/Customer Service Liaison, Develop detailed methods for repairs and rework processes as needed, Create clear SOPs to explain repair/rework methods (with support from Technical Writing team on final format), Lead technical assessments to define ‘manufacturer approved’ component modifications and methods; prepare SOPs for service centers to execute key modifications, Bachelor’s Degree in a process engineering-focused discipline (Chemical, Mechanical, Materials, Manufacturing Engineering), Minimum 3 years of hand-on experience with composites manufacturing, testing, or failure analysis, Direct experience leading problem solving or process improvement teams – you must be action-oriented with a hands-on approach, Excellent technical writing and documentation skills, Experience with outsourced manufacturing, especially with Asian suppliers is preferred, Familiarity with formal Quality problem solving techniques is highly desirable, Ability and eagerness to work in a fast-paced environment with constant innovation and aggressive timelines, Avid cyclist and bike mechanic, passionate about our products, Compile validation protocols, IQ, OQ and PQ documentation relating to the manufacturing cycle, Provide quality assistance with testing, monitoring and maintenance or clean rooms and other controlled environments, Ensure adherence to regulatory requirements to ISO and FDA, Work with suppliers for new processes, quality issues and process improvements, Representing quality to assist with company projects across the board, 2-3 years' experience as a QE in a manufacturing environment, Over 1 year experience in the medical device industry, Strong knowledge of relevant regulatory standards, Drive quality improvement in the factory using, ACE Tools (Relentless Root Cause Analysis, Mistake Proofing etc. Conduct Quality Training as appropriate per Diebold Nixdorf Reliability Manual, Assist with the implementation of quality improvements and associated projects using advanced quality tools (for new products/sub-assemblies and parts), BS degree in Engineering or Natural Sciences, Experience in a systems engineering role desirable, Competent is one or more statistical analysis software packages (Minitab, JMP, Reliasoft, etc), Minimum of 7 years in a NPI/NPD quality or equivalent role, Product design engineering experience of low to medium volume manufacturing of electro-mechanical products highly desirable, Able to use and instruct others in the use of MSA (GR&R), Cp/Cpk studies, Control Plans, CAPA, etc, Working experience in GDT and design for assembly/manufacturability of complex assemblies highly desirable, Critical thinking, sees the big picture and drill down to components of it, Excellent communications (oral, written, presentation) skills at different organizational levels, Leadership skills & presence/soft skills required, CQE , Six Sigma certification highly desirable, Represent Quality on strategic cross-functional initiatives/teams. (Personal Protective Equipment). Serve as primary Nascote contact for assembly plant customers and liaisons, Investigate warranty concerns and issues and coordinate responses to customer and corrective actions as required, Updates and reviews customer requirements with the Quality Technicians, Gage design review, approval and implementation. (speech and writing), Providing Quality Engineering support for the Fairfield OH98 site, (Customer) Internal interface for Returned Sales providing Failure Analysis and Corrective Action, Lead Root Cause and Corrective Action activities through a combination of data driven analysis and applied engineering knowledge, Act as site Quality Management System representative, responsible for generation of local site documents and compliance with S&PS procedures, Support of Key Operational Metrics with emphasis on Complaint turnaround time, dPPM, COPQ and other site metrics, including reporting weekly in TeamGuru & monthly in OBF & MOR meetings, Mentor/coach production and support direct and indirect labor team members to drive efficient RCCA improvement (Rapid Problem Solving), Pro-active support of production quality through Honeywell Operating System (Lean methodology), Bachelor’s Degree in Engineering or Engineering Technology and Three (3) years of experience in Quality, Design or Manufacturing engineering with exposure across multiple functions, Experience with Printer Media products and customers strongly preferred, Good communication skills to both internal and external customers, both written and verbal, Competency in drawing/print review and internal/external technical customer requirements documents for flowdowns and applicability is preferred, Must be able to lead technical discussions with diverse, cross-functional groups to reach consensus and document these conclusions, Candidate should be motivated to Champion Change and seek process improvements, while assessing trade-offs to ensure Intelligent Risk-Taking, IS09001 Quality Systems knowledge is preferred, Prior knowledge of SAP Quality Module, to support current planning and Q1 2017 deployment, Leverage available data to make informed decisions using Six Sigma tools and methodologies, Results focused with successful record of accomplishments through skilled use of influence, persuasion, negotiation, and problem resolution, Excellent team building skills, ability to lead and thrive in a matrix environment, Ability to read and understand contract quality requirements, and HTSI policies, procedures and processes, Experience with Six Sigma tools, Green Belt preferred, Experience Supervising other Quality personnel, BA/BS degree in a technical discipline (i.e., engineering, computer science, quality assurance) with 5 years of Quality Engineering experience, Experience using Honeywell specific software/management tools (ECATs, PDM, One Source, SAP, NetInspect, etc.) Specific vision abilities required by this job include depth perception. In our sample resume objective for Quality Engineer, we try to clinch the deal by disclosing the information that Aaron is a certified Quality Engineer with 9 year experience. Resume Builder. Incoming raw material inspection instruction preparation. This includes knowledge of, and experience with, applicable standards, GxP requirements and regulations. Participate or lead quality improvement projects, Development of projects and application of QE techniques and methodologies providing technical expertise and support to QA and other functions, Conduct analysis of data and recommend appropriate action, performs audits and capability studies as necessary, Works with the plant, packaging development, technical packaging, and other parties to define critical requirements. Includes process development, risk management, qualification of equipment, and validation of processes, quality planning including inspections, test method development, some level of software validations, and Supplier quality requirements, Advanced understanding of quality systems, statistical techniques, and risk management (considered the ‘go to’ technical person), Lead and direct the project team applying quality tools and methods that improve efficiencies and effectiveness for design and process development, Responsible for quality systems maintenance and improvement, Trains technical staff in quality systems, Initiate and lead in the investigation of highly complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes based on engineering principles; analyze results, make recommendations and develop reports, based on engineering principles, Drive the development and manage the execution of multiple, highly complex experiments and tests (including writing and executing protocols) to create, validate, and improve products (including evaluation of source materials and suppliers) and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports and lead team members to drive project completion, Lead in the identification and ensure the optimization of highly complex Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. No need to think about design details. Crafting a Supplier Quality Engineer resume that catches the attention of hiring managers is paramount to getting the job, and LiveCareer is here to help you stand out from the competition. Quality Engineer Resume Examples. Quality Assurance Engineer Resume - Sample 3. It’s actually very simple.

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