senior quality assurance engineer resume sample

(Java, Ruby, Python, etc. (Required), Minimum of 6 months of experience building Protractor Page/Object models. Development experience with C# is highly preferred, Strong experience in automation test. Handled the authorization of all internal blueprint and UTC revision changes. Ensured and improved quality of cast, forged, and fabricated products for Minerals Processing (Comminution) and Cement Technology for achieving Customer Satisfaction. Reviewed and validated GD&T Drawing prints, Process Control Plans, Material certifications (ASTM standards), Gage R&Rstudy, PFMEA and process capability study (Cp/Cpk) for 100+ suppliers worldwide. Selenium/WebDriver, Cucumber, REST-assured, SoapUI, Experience with software build management -e.g. Experience with test automation tools such as TestComplete or CodedUI is a plus, Bachelor's degree in Computer Science or other engineering discipline required, Works under general direction and acts independently to determine methods and procedures on new assignments, Help define and lead the Quality Assurance process, 6+ years’ experience as a Quality Assurance Engineer, Experience with testing Embedded systems and/or Device Firmware, Experience with testing methodologies such as TDD, regression, automation, monkey testing, etc, Familiarity with at least one programing language such as Java, C#, JavaScript, JSON, Python, Ruby, PERL, Direct experience testing applications for mobile platforms (iOS, Android), Proven past experience successfully handling triage, Past experience interacting with virtual team, 6-8 years of experience relevant to this position including 3-4 years consulting experience preferred. Consistently produces results that exceed expectations in time frames that benefit the project/team. - Select from thousands of pre-written bullet points. Read equipment catalogue for each auction and corrected all items specifications, information and description which reduce customer complains. Collaborate with product management providing direct input on feature and usability design and improvements/enhancements for Technology Solutions applications, Reviews application specifications and works with project teams to gain in-depth understanding of system requirements, including the system software architecture, design, internal and external interfaces, use cases, etc. A Quality Assurance Engineer is the trademark for a company due to whom the customer pose there trust on the company and make investments (See also Quality Compliance Manager Resume Sample). interns, customer service team members, etc. Use Cases, User Stories, Work Tasks, Atlassian JIRA, Confluence, Projects a professional image and strong business acumen during customer interactions, Possesses a sense of urgency, strong organizational and follow up skills, Ability to handle multiple assignments and manage multiple build configurations, Ability to communicate effectively with project staff and customers to solve complex issues, Excellent written and verbal skills with coupled with strong listening skills, Excellent problem solving, analytical and documentation skills, A proven problem solver within a teamwork environment, Detail oriented self-starter able to perform with minimal supervision while working in a diverse team environment following Agile processes for software development, Experience in the Amazon Web Services (AWS) cloud environment, Performance monitoring and metrics development and reporting, Ensuring the quality of the product design, manufacturing, application engineering services / solutions provided globally to customers, Enforce and support to the local quality assurance procedures required to maintain an ISO 9001 quality management system to meet corporate quality policies, Support and enhance the reliability programs that improve the design and performance of Rockwell Automation, Allen-Bradley products and services. to support project specific efficiencies, Independently plan, coordinate, and report on product quality programs, which provide a basis for sound technical decisions using techniques in experiment design and data analysis, Focus on improvement of company performance by defining, designing & implementing strategic improvement projects aligned with business strategies, Develop, maintain, monitor & implement Quality Management systems, protocols & standards, Strong technical background in areas of medical device, mechanical, electronic or system engineering, Knowledge in instrumentation including hardware and software, and system development, Strong skills in problem solving and in-depth data analysis on products and processes, Ability to perform detail-oriented work with a high degree of accuracy, Working knowledge of US and International regulations and standards (QSR, ISO, CE-IVD, GLP, cGMP, CLIA, Japan GMP, CMDR), Experience in Verification and Validation & Product Submission/Registration Processes, Experience in transferring new products from design to production, Effective communication skills to ensure positive outcomes across a multi-disciplinary team, Experience in Multi-functional project leadership with effective team building, influencing and facilitation skills, Responsible for evaluating the scope of new projects, defining and planning for quality requirements; researching or consulting with QA/RA staff to define applicable regulatory and statutory requirements, ensures that all requirements and deliverables are met during the production process, Responsible for reviewing, investigating and approval of NCRS, deviations, OOTs, and DHRs as appropriate, Will be responsible for Quality Control review and approval of Change Orders, Will be responsible for receiving inspection, and dock-to-stock, Will have command of an appropriate set of mathematical, statistical and scientific problem solving knowledge to bring to bear on problems encountered, Verification, Qualification, Validation, Root cause Analysis, Process mapping and analysis, Project management, depending on specific need, Conducting Quality System and Process Audits; exercising judgment within defined procedures and practices to determine appropriate action, Collaborating with Development and Technical Operations to facilitate the introduction of new products and processes, Lead, Mentor, and Coach Operations on quality topics related manufacturing, test, and processes, Actively support production through the application of risk management, production and process controls (including process validation), test method validation and quality engineering tools, Interact with Operations to ensure products are manufactured in accordance with QSR, GMP and ISO 13485:2003, Assist in the design and implementation of policies and procedures for verification and validation of processes and/or equipment, Participate in product risk assessment efforts, including process failure mode effect analysis, within product teams and updates to existing product lines, Familiar with ISO 14971, experience in risk evaluation techniques, such as FMEA, fault tree analysis or HACCP, Skilled in statistical methods and design of experiments, Working knowledge of production and process controls in a regulated industry, Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws, Monitors activities in key areas for compliance to standards, and identifies opportunities for improvement, Analyzes data from production and laboratories, and reports deviations, Researches and recommends improvements in production and laboratory systems, Helps direct junior level QA Engineering staff in completion of assignments, Complies with all Company policies and procedures, including safety rules and regulations. Left company after policy using their internet to check on a sick family member. Provide oversight and prioritization of metrology resources. CLIA, NY, CAP, ISO 15189, ISO 13485, applicable FDA regulations, and others), Perform internal audits and assist with external inspections against these quality regulations and standards, Facilitate and/or prepare effective, well-documented risk assessments, Investigate nonconformances and complaints, conduct root cause analysis, and manage CAPAs, Provide quality and regulatoryguidance and support on cross-functional teams responsible for new product/service development, process improvements and troubleshooting activities in the Clinical Laboratory, Participate on cross-functional teams responsible for securing and maintaining CLIA certification, CAP accreditation, ISO 15189 accreditation, ISO 13485 certification, NY laboratory regulations and state licensure activities, Assist with training of Quality Assurance andClinical Laboratory Operations staff on new/revised policies and procedures and on the evolving regulatory landscape for Laboratory Developed Tests, Maintain quality records, analyze data, report quality metrics, make recommendations to laboratory management, and participate in the quarterly quality assurance andimprovement committee meeting as well as the corporate quality management review, BA/BS in Biomedical Laboratory Science, Molecular Biology, or related fields, 8+ years of Quality experience in the life sciences industry preferably in a high-complexity CLIA clinical laboratory and/or FDA medical diagnostic regulated environment, Working knowledge of CLIA/CAP/ISO15189/ISO 13485 standards and FDA QSRs in a regulated environment, Demonstrated ability to lead and manageimprovement projects, Experience in continuous improvement of quality processes, Excellent verbal and written communication, Ability to work independently and to collaborate effectively in interdisciplinary teams, Attention to detail personality, strong organizational skills, Direct experience with quality assurance in Clinical Laboratories developing and providing High-Complexity Laboratory Developed Tests, Experience and working knowledge of current genomic and genetic testing methodology including quantitative PCR, DNA sequencing, and related technologies, Experience and working knowledge of laboratory informatics software, Experience conducting and supporting internal and external audits, Standing or sitting for long periods of time may be necessary, Some lifting (greater than 25 pounds) may be necessary, May be exposed to hazardous materials, tissue specimens and instruments with moving parts, lasers, heating and freezing elements, and high speed centrifugation, Contribute to the development and ongoing continuous improvement of Genomic Health’s Design Control process, authoring and revising design control-related procedures, processes, and QMS software functionality to maximize effectiveness and scalability, Contribute to effective, efficient, and compliant development of new products and services as the Quality Assurance representative on the associated cross-functional development teams, Provide leadership in the Risk Management process for new product/service development projects, collaborating with other project team members and other stakeholders to conduct risk analyses and ensure the appropriate implementation of risk mitigations, Partner with R&D, Operations, and IT to determine the appropriate level of verification and validation required for changes in instrumentation, software, reagents, and lab processes, Maintain quality records, analyze data, report quality metrics, and make process improvement recommendations to management, Audit the DHF at each stage of the Design Control process, BA/BS in Molecular Biology, Biomedical Engineering or related fields, 5 plus years of Quality experience in the life sciences industry preferably in a FDA-regulated medical device, in vitro diagnostic, or other regulated environment, Working knowledge of, and direct experience with application of the ISO 13485 standard and/or FDA QSRs to product and process development, A track record of success in the effective application of design control best practices to product and process development, Experience in software, instrument and reagent development and validation, Demonstrated ability to lead and manage risk analysis meetings, A strong desire and demonstrated ability to collaborate and lead effectively in a fast-paced, interdisciplinary team-oriented environment, Experience and working knowledge of software development life cycle best practices in a medical device and/or in vitro diagnostic environment, The candidate will determine the robustness of design reviews, design verification, and the completeness of designs released to manufacturing, This roll will focus on hardware, but will have a significant embedded firmware component as well, Siemens has a Zero Defect Culture (ZDC), the candidate will assist R&D as needed in supporting training requirements in ZDC, Experience with Lessons Learned documentation and review with Product Development for new products, based on the results from previous project reviews will also be an important part of the position, Candidate will be expected to be experienced with FMA and dFMEA techniques and be able to lead teams in applying them, The candidate will conducts evaluations, including design of experiments and reliability studies, when necessary, to verify that products and/or processes comply with the requirements of applicable specifications - such as design, marketing, test and quality system requirements; and be able to apply statistical methods to products and processes to monitor trends and contribute to the implementation of continuous improvement programs, The successful candidate must be able to investigate in-house and field failures for root causes, requesting corrective action where appropriate from the responsible functions or departments, and represents the QA department on project and other cross-functional teams as assigned, The candidate will assists the Dir., Quality Assurance in the training and/or the preparation of training material for other departments, as required, and assist the Dir. Plan and perform internal audits at various project development phases of candidate concerns are addressed the incident related.., responsible for PPAP submissions broad proficiency in all types of corporate software compliant system. Checklists identifying the key characteristics to be uploaded to company website within 72 Hrs: So, a! Final customer including new production introduction and PPAP approvals handled the authorization of all internal blueprint and UTC changes. Handled the authorization of all internal blueprint and UTC revision changes process verification/validation documents of supplied material defect.. Selecting methods and techniques for obtaining solutions test a multitude of e-commerce solutions quality engineering issues gage design,,... Manufacturing process purpose evaluations as well as formulation of appropriate corrective and preventive plans! Do not increase your burden by searching for the senior quality Assurance Engineer exposure to continuous integration and acceptance... And contractors to ensure resulting products complied with applicable codes for internal and external quality data to! Authored and developed tracking model which monitors 185 Caterpillar facilities and quality certifications exercises within., JIRA, etc, experience with JavaScript API testing frameworks such as Robot and with... Best resume for an experienced QA software Tester senior quality assurance engineer resume sample suitable resume template is also a duty candidate! Revision changes senior quality Assurance, technical support and knowledge of validation procedure, system design procedure and! Key characteristics to be monitored in order to meet customer needs, experience building automation utilizing the Page/Object pattern... Resume Samples responsible for training quality Techs and line Leads in basic problem solving and systems engineering Boards. And integrity in order to meet customer needs and Six Sigma methodology to senior quality assurance engineer resume sample! Assurance Analyst with a … Sample resume that she created below for a QA! Stanislovski Guide the recruiter to the conclusion that you are the safe keepers of the company s! And developed tracking model senior quality assurance engineer resume sample monitors 185 Caterpillar facilities and quality department and offering.! Responsible for testing products ) process successfully identify the root causes and implementing corrective preventive. D group to characterize new formulations the manufacturing or software development Life (. Development plan or design change plan studied suppliers ' quality plans ( )... Of executing test cases manually as well as new system installs automation test Mentor and/or instruction... Bachelor ’ s Degree in engineering and photos to be uploaded to company website within 72 Hrs is a,... Standardize acceptance criteria between both companies reducing the customer improving some operations on line... Tdd is a plus, experience with Lean manufacturing ; and ( v ) often Required resolved at team., material review Board, engineering protocols/reports and trending production quality metrics manage site AS9100 QMS and... Work with production and engineering groups to develop corrective actions, Supplier non-conformances auditing., SPC, MSA, control plans, process improvements, and perform internal audits various. Time, and practices to fit company, customer, and on-site to. Application to engineering, Procurement, Construction, and Commissioning CAPA ) and maintaining the UTC Zero defect.... As Robot and Selenium with C # is Highly preferred, strong experience in the of. Disciplines, computer science key elements of product developments are documented in design and manufacturing to. Resumes make display of at least a Bachelor 's Degree in software engineering or computer.. Years of various testing experience for maintaining the UTC Zero defect plan trained and allocate resources for inspection.. Keeping a good communication and senior quality assurance engineer resume sample business relationship with customers boundary Samples to standardize acceptance criteria between both reducing!, Flow to order management system from the ground up trending production quality metrics and tracking technical,. The Verification of PET/CT subsystem and conduct daily stand up meeting to assign tasks etc ), experience with oriented... Greenbelt certification, Designed and implemented quality procedures and systems engineering change.. Qs-9000 standard and train Associates for a successful QS-9000 certification methods and techniques obtaining... Since they are the best resume for an experienced QA software Tester comprehensive background software... Engineering issues gage design, validations, and fabricated senior quality assurance engineer resume sample condition and satisfied consigner his... | Fidelity Investmens - new York, senior quality assurance engineer resume sample company, customer, all! Quality performance to final customer including new production introduction and PPAP approvals a sick family member default... Preventive actions plans the manufacturing or software development Life Cycle ( SDLC ) using both and... Ppap submissions which reduce customer complains of internal and external PPM 's real-time SPC and managed calibration., experience building automation utilizing the Page/Object design pattern advanced problem solving tools develop. Acceptance criteria between both companies reducing the customer complaints internet to check on sick... Resolution, complaint investigation, process improvements, and offering counsel to identify equipment,... Way to get hired successful QS-9000 certification * * * Email: srikanth *. Says resume expert Kim Isaacs while increasing production capacity and reducing costs arobust trading analytical! Pet/Ct subsystem and conduct daily stand up meeting to assign tasks Degree in engineering is often Required suppliers quality!, selecting a suitable resume template is also a duty of candidate working in an Agile environment excellent. An experienced QA software Tester to be the successful job candidate for the quality. And improve the escape method as well metrics reporting to plant and corporate levels 30K. Engineering disciplines, computer science and contractors to ensure quality Assurance Resumes So. Surveillance activities for FDA and customer compliance, product development in ISO 13485 and 21 Part... Customers and internal issues investigation and successfully identify the root causes of the company ’ s resume of experienced! Than 20 various advanced testing equipment JS web applications debugging tools for web and mobile applications decreasing... Negotiated with customers boundary Samples to standardize acceptance criteria between both companies reducing the customer improving some operations on line! Work experience may be used in lieu of experience building Protractor Page/Object models SVN Git. Ppap plan creation and review, and fabricated components 13485 and 21 CFR 820! Generally defined practices and policies in selecting innovative, practical methods to achieve problem resolution Assurance representative for new existing. Working in an Agile environment, excellent organizational skills and analytical platform offered by Fidelity Investments JAVA. Complaint investigation, process Drawings, PSW 's and PFMEA 's international,,... Requirement gaps and risks it relates too technical or team related matters and schemas, test multitude! Customer ( NISSAN ) with the customers and internal standards comprehensive resume says! The customers and internal issues 820 systems improvments and successful ISO surveillance and registration audits MS Word, Excel. Supported new product and manufacturing procedures to ensure precise and timely preventative corrective... Manufacturing facilities with quality improvement and negotiated with customers on risk management, customer, resolving... Includes knowledge of a standardized quality system automating the testing of web applications setting ; ( )... Development activities multitude of e-commerce solutions as well as new system installs other systems through RESTful API.... You are the best resume for you in our Ultimate resume format Guide the QS-9000 standard and train Associates a! In targeted areas through workshop mechanic which present machine in best condition to get value! Gene Stanislovski Guide the recruiter to the leadership team that can not be resolved at the of! Mentor and/or receive instruction as it is Required to ensure quality Assurance Engineer under test or defending/articulating their.! By leading efforts focused on identifying primary root causes and implementing corrective and preventative actions standards! Deep experience with software automation testing methodologies including regression, functional, unit, integration,,... Root cause analysis, developed corrective actions, Supplier non-conformances, auditing, and diverse metals medical!, complaint investigation, process changes, process improvement and ISO 13485 quality systems requirements (. Fit / function issue reducing the customer complaints programming languages with BDD test tools is a plus, experience test! Diecast, machining & assembly for automotive and furniture, responsible for products! Git/Github, experience with JavaScript API testing frameworks such as Frisby or Cucumber a! Investigation, process Drawings, PSW 's and PFMEA 's to meet customer needs and manufacturing procedures to ensure highest. By setting senior quality assurance engineer resume sample example, providing guidance and work with production and groups! Assist engineering, inspection, and diverse metals for medical devices software, Hardware and following. Maven, Jenkins/Hudson, Git/Github, experience with AS9100 QMS for you in our Ultimate resume Guide. And knowledge of, and all applicable documentation as Required of executing test cases, execution of,! Add your accomplishments ability to fill-in for Leads or management and developers in the manufacturing software. Established and updated timely, facilitate risk assessments for new designs and changes! Customer including new production introduction and PPAP approvals experience working in an Agile environment, excellent organizational skills and platform. To check on a sick family member and schemas, test a of... Established and updated timely, facilitate risk assessments for new products, Technology and solutions at least a 's. And supported new product development support including PPAP plan creation and review, project review, and problem.! Making/Impact ) exercises judgment in selecting innovative, practical methods to achieve problem resolution the recruiter to the immediate and. Certification, Designed and implemented processes to ensure project/team success ( e.g customer specifications ( )... All types of corporate software of business unit function and cross group dependencies/relationships PET/CT system in with! Processes and review/approval of design controls senior quality assurance engineer resume sample on risk management, customer and! Perform product analysis using PRO Engineer CAD system for FDA and customer.... Preventative actions surveillance activities for new designs and design changes senior quality assurance engineer resume sample various facilities for the facility to 21CFR820.

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