Quality Assurance Engineer Jobs in Indiana

Job Title: Manufacturing / Quality Engineer Company: Navistar Location: Wakarusa, IN Description: To develop assembly processes and conduct Quality assurance and control activities related to internal quality management system and supplier processes and components.  Determine tooling and equipment requirements to build new products; and to execute and maintain build process documentation including operator instructions. Basic Requirements: Bachelor's Degree in EngineeringAt Least 3 years of engineering experience Additional Requirements: US Citizenship or Permanent Resident status requiredTravel less than 10%, may require flexibility due to short notice Desired Skills:Positive Attitude, Ethics, and Navistar Values which support our company’s values, and a healthy, high performance cultureBachelor’s Degree in Manufacturing, Industrial, or Mechanical EngineeringSelf starterAbility to work as an individual or as a part of a teamGood written and verbal communication skillsBasic computer skills with Microsoft Office programsSkills in AutoCAD, Unigraphics or a similar CAD package are a plus Visit us at www.Navistar.com to discover more about our organization. We are an Equal Opportunity Employer. The Future Rides On Us

Job Title: Quality Engineer 2 or 3 Company: Honeywell Location: South Bend, IN Description: Field Quality Engineer Description:In this role, you will be required to work directly with suppliers to satisfy Honeywells quality standards and strategy in the manufacture of aerospace and engine components. As a field Quality representative, you will be required to interact with all levels of supplier management. Organizationally, you will report directly to the Manager, Field Quality Engineers. You will be expected to travel in support of a variety of supplier oversight functions, spending a majority of your time at supplier facilities. As Honeywells point of contact within the supply base in direct support of OEM site requirements, you will:Provide technical leadership to coordinate implementation of advanced quality processes including statistically based variation reduction, control planning, mistake proofing, and Manufacturing Process ControlEvaluate prospective supplier Quality Systems and conduct Gap Analysis where requiredEvaluate procedures for compliance to contractual and regulatory requirements (including international regulation coordination issues)Prepare and present metrics associated with quality trends and related improvements within the supply base. Prepare progress reports, program reviews as needed, to assure the highest quality and cost effectiveness from the suppliersTrain associates, suppliers, and contract personnel in Six Sigma techniques, Manufacturing Process Control, variation reduction, etc.Success Factors:You will be responsible for quality assurance processes including, but not limited to, First Article Inspection Requirements (FAIR), Self Release and product audits, as well as coordination of Quality System (AS 9100) compliance audits and special process oversight. In addition, you will be responsible for training and deployment of Manufacturing Process Control, variation reduction, quality requirement compliance, Six Sigma, and other Honeywell sponsored supplier initiatives.

Job Title: Manager- Manufacturing Quality Engineer Company: Bayer Location: Mishawaka, IN Description: HealthCare Manager- Manufacturing Quality Engineer Bayer HealthCare (BHC) makes an important contribution to human and animal health with its innovative products and by researching new therapeutic approaches. Our Specialty Pharmaceutical business ranks among the top 10 specialty pharmaceutical companies worldwide. Our global research and development is focused in five distinct areas: Diagnostic Imaging, Hematology/Cardiology, Oncology, Specialized Therapeutics, and Women’s Healthcare. As a specialty pharmaceuticals company, we at Bayer HealthCare focus our efforts where we can have the most impact. Our Diabetes Care division is one of the largest self-test diagnostic businesses in the world, supporting customers in 100 countries. Our Consumer Care business is a top competitor in many important product categories including analgesics, cough and cold, and nutritionals. More than 3,000 employees support 14 manufacturing sites in 11 countries dedicated to ensuring the delivery of a secure, high-quality, cost-effective supply of our products around the world. Our Animal Health business in North America is dedicated to making the world a better place for our veterinary customers, their clients, and the animals well all hold dear. Job description The primary responsibility of this position  is to oversee the quality processes and quality engineering group that support Diabetes Care Mishawaka manufacturing, OEMs and contract manufacturers/packagers.  This position is responsible for assuring that the quality of manufacturing and release processes meets or exceeds customer expectations, including regulatory requirements. The Candidate will: Direct quality engineering activities supporting Diabetes Care Mishawaka manufacturing and contract manufactures and coordinates best practices with other Diabetes Care manufacturing sites; Optimize process control and documentation practices to simplify quality documentation while minimizing risk to product quality; Provide quality direction to key production support groups including Corrective and Preventive Action Teams (CPATs), Validation Approval Team (VAT), Process Software Configuration Control Board (CCB) and Product Supply Business Unit Managers; Interface with Supplier Management to ensure alignment with quality practices at suppliers, contract manufacturers and OEMs; Serve as the accountable quality decision maker for production issues arising from Product Supply, Marketing, R&D and QA/RA; Develop measures to monitor manufacturing quality for continuous improvement and effectiveness of root cause investigation/corrective actions; Provide professional growth opportunities for quality engineering staff; Your qualifications The selected candidate is required to possess the following: Bachelor's in the Sciences, Engineering or Life Sciences with 10 years relevant job experience; Strong Management experience; Ability to manage senior scientists and engineers with a focus on personal development in addition to technical development; Applying quality system principles to a production environment including management of nonconforming product/process, technical approval of engineering changes, implementing corrective and preventative actions (CAPA), verification/validation of product/process improvements;   Working knowledge of SPC, Six-Sigma, TQM or comparable process management tools with Minitab experience desired. Understanding of production documentation including Bills Of Materials (BOMs), Device Master Records, Device History Records production process orders; Strong computer skills including use of Microsoft Word, Excel and PowerPoint.  Database experience a plus; Previous healthcare FDA/ISO experience; Effective written and verbal communication skills; Strong interpersonal skills, including the ability to work with and influence individuals of diverse backgrounds and technical abilities; Ability to make sound quality decisions under pressure; Preferred skills: Six-Sigma Black Belt and/or ASQ CQE/CQM certification preferred; Experience with SAP preferred; Previous medical devices; Strong background in process/equipment/facility validation preferred; Masters degree. Your application We offer a wide variety of competitive compensation and benefit programs. In addition to a competitive base salary, you will be eligible for an array of innovative rewards and recognition programs, variable pay and incentive opportunities as well as benefits coverage beginning on your first day of employment. We are committed to helping our employees maintain a healthy balance between their responsibilities at work and home. You will be eligible for paid time off programs, paid company holidays, flexible work options and numerous site conveniences. We are also committed to supporting your professional development through career ladders, training programs, tuition assistance and professional association events. If you meet the requirements of this unique opportunity, we encourage you to explore how you can make a difference at Bayer by applying now. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. www.myBayerjob.com                                             Phone + Register to View Bayer is an Equal Opportunity EmployerReference Code:   Register to View Location: US-IN-Mishawaka

Job Title: Quality Engineer Company: Peoplelink Staffing Solutions Location: Warsaw, IN Description: Job Summary: Position is responsible for supporting quality assurance and statistical process control in manufacturing and new product development with hands-on approach as a team member throughout all phases of projects, FDA and ISO regulated. Essential Duties: Develops and initiates standards and methods for inspection, testing, and evaluation. Plans and conducts the analysis, inspection, design, test, and/or integration to assure the quality of the assigned product or component. Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data. Applies statistical process control (SPC) methods for analyzing data to evaluate the current process and process changes. Documents data obtained during all quality activities consistent with company policies and procedures. Develops gauging applicable to products and tolerance. Initiates corrective and preventive action (CAPA) plans with root cause analyses. Communicates significant issues or developments identified during quality activities and provides recommended process improvements to management. Develops quality plans as needed. Directs technical and administrative workers engaged in quality activities. Maintains a working knowledge of government and industry quality codes and standards. Performs related duties as required. Requirements Job Specifications: Requires the ability to Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to effectively present information to Team Members with an emphasis on training. Ability to comprehend and apply principles of advanced calculus, modern algebra, and advanced statistical theory. Ability to work with concepts such as limits, rings, quadratic and differential equations, and proofs of theorems. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, factor analysis and statistical process control. Skills And Abilities: Knowledge and skills identified are typically acquired by completing a Bachelors degree (BS) or higher and 3-years experience in medical product quality assurance. Must have a working knowledge of statistical sampling, blueprint reading, gauging concepts, and geometrical dimensions and tolerance. Must also have a working knowledge of FDA/ISO regulations as they relate to medical devices. All qualified candidates should send their resumes to David Neff at Register to View .

Job Title: QA Engineer Company: Sahasra Technologies Location: Indianapolis, IN Description: We are looking for a Quality Assurance Engineer. Face to face needed. Mandatory skills are:- Develop Test Cases, Test scripts, Use cases- Define Test Requirements, Systems Acceptance Testing and Regression Testing- Experience in reviewing .Net/C# applications and web service based testing- Good Knowledge in Visual Studio and Team Foundation Server- Extensive knowledge of QTP- Excellent knowledge of SDLC processes preferably Agile Responsibilities: - Write, implement and report test scripts, and use cases- Evaluate and implements test tools and strategies. - Develop, maintain, and upgrade test scripts- Analyze test cases and provide progress reports. - Extensive knowledge of QTP- Migrate existing manual test cases in Quality Center to automated test cases

Job Title: QA Engineer - Software Quality Assurance - C/C++ -... Company: Cybercoders.com Location: Indianapolis, IN Description: QA Engineer - Software Quality Assurance - C/C - OS-level QA Engineer - Software Quality Assurance - C/C - OS-level - Java - Assembly - compilers - Skills Required - software quality assurance, SQA, QA, software QA, tester, test engineer, engineer, analyst, compilers, linkers, loaders, C/C , Java, Ada, Assembly, automated test, test automation, automation, GCC, Visual Studio, Xcode, Eclipse, JDK, debuggers, disassemblers, PE, ELF, DWARF , dylibs, bundles, Ant, Ant scripting, Agile, UI validation, user interface validation, security, security clearance, mission critical software, security investigation, clearance QA Engineer - SQA Analyst - Tester - Software Quality Assurance Engineer - compilers - linkers - loaders - C/C - Java - Assembly - GCC - Visual Studio - Xcode - Eclipse - JDK - automation - Agile - security - Ant - Test Engineer If you are a QA Engineer with prior C/C or Java coding experience and strong experience working/testing at the OS-level, please read on!Stable, growing firm in the West Lafayette area seeks an operating-system-level Test Engineer with 3 years of experience to test the next generation of its products. Relocation assistance will be considered for top candidates. What you need:- In depth experience using compilers, linkers, and loaders (GCC, Visual Studio, Xcode, Eclipse, JDK)- Experience testing compilers is highly preferred, but not a requirement- Ability to construct and adapt tests in C/C or Java- Extensive experience working at the operating-system level with Windows, Linux, or MacOS- Understanding of Assembly language; experience with debuggers and disassemblers- Understanding static and dynamic libraries, the various file formats of executables and libraries (PE, ELF, DWARF , dll's vs exe's,. so's, dylibs/bundles)- Experience with Ant scripting- Experience with GUI test automation- Experience with software security What you'll be doing - You will:- Design and implement tests of product, applying software protections to various compiled software programs and libraries- Port, adapt, and create the compiled programs that the tests operate on- Isolate and eliminate compiler and system interactions between programs and libraries, linkers, loaders, and other OS-level facilities and servicesWhat's in it for you:- Stable and growing company- Excellent, comprehensive benefits- Opportunity to work in a strong team environment with an accomplished group- A company that serious about moving quickly to hire top talent So if you are a Software QA Engineer with prior C/C or Java coding experience and strong experience working/testing at the OS-level, please apply now! - JO-IN. QA - , , , , , CyberCoders CyberScientificJob type: Full Time.

Job Title: Quality Engineer Company: Parker Hannifin Location: Goshen, IN Description: Advocate and support the Corporate WIN Strategy by managing the quality operations in the assigned Value Stream.  Develops, modifies, applies, and maintains quality standards for products and processes.  Provides statistical information for quality improvement by gathering data on trends and root cause analysis.  Responsible to guide technical evaluation, analysis, and  related data acquisition processes to ensure plant quality objectives are achieved. Essential function are: Assesses quality performance using statistical and analytical methods.  Devises and implements various methods and procedures for inspecting, testing and evaluating the precision, reliablity and accuracy of products, processes and production equipment. Develops and establishes quality systems and procedures, inspection plans, quality performance trends, statistical plans, cost estimates and technical quality plans for proposals.  Ensures that project and/or process control documentation is compliant with requirements and/ or contract. Assesses the cost of, and determines the responsibility for products, or materials that do not meet required standards and specifications by performing  statistical analyses. Provides input on quality to product development teams. Identifies quality performance, trends and corrective action by coordinating with customers and suppliers.   Ensures compliance to specified quality requirements by performing in-house and supplier audits and surveys.  Develops and initiates programs to improve supplier performance. Prepares reports by collecting interpreting, analyzing and summarizing data and making recommendations.  Analyzes proposed changes in methods and materials.  Compiles and writes training material and conducts training sessions. Participates in failure analysis and corrective action investigations. Refines and enhances products and processes by appllying continuous improvement and key lean manufacturing/procution principles and techniques to critical areas of production. Communicates and educates Value Stream Team on matters requiring specialized knowledge of quality functions,i.e.c PPAP, APQP and document control. Makes quality -related customer and vendor visits and contacts as required. Maintains professional and technical knowledge by attending workshops, reviewing publications, establishing industry networks, benchmarking state-of-the-art practices, maintaining American Society for Quality certification

Job Title: Senior Quality Assurance Engineer Company: Beckman Coulter, Inc. Location: Indianapolis, IN Description: Beckman Coulter develops, manufactures and markets products that simplify, automate and innovate complex biomedical testing. Our diagnostic systems are found in hospitals and other critical care settings around the world and produce information used by physicians to diagnose disease, make treatment decisions and monitor patients. Instruments for life science research are used by scientists as they study complex biological problems including the causes of disease, identify new therapies, and test new drugs. Our customers include hospitals, physicians' offices, diagnostic reference laboratories, pharmaceutical and biotechnology companies, universities, medical schools and research institutions. In fact, Beckman Coulter has more than 200,000 clinical and research instrument systems operating in laboratories around the world.The Senior Quality Assurance Engineer will lead the Software Quality Assurance efforts on a product development team.Represent QA on development, current business or product improvement projects. Provide oversight and review of the software product development process and risk management concepts ensuring regulatory compliance. Assure product quality readiness from requirements through design transfer. Provide input to budget process and project schedules. Coordinate complaint management activities and Customer Feedback failure investigations. Review, implement, or revise product, project, and program quality activities. Provide design review and risk assessment expertise. Develop validation plans and protocols to assurance products meet user needsOperate analyzers and other lab equipment to support product evaluation Expertise in the following areas is required for consideration:Degree in computer science or software engineering. Chemistry, Math or related sciences a plus. Demonstrated familiarity with object oriented design Software development and software risk management experienceC++, C# and Visual Studio experience – preferred Experience with BCI analyzers – a plus Demonstrated abilities for consideration:Proven track record in software quality assurance, product development, verification, and validation Deep understanding of software life cycle processes, especially requirements elicitation and software validation Proficient in conducting software development process audits FDA and ISO compliance experience (especially QSR, Part 11, Quality System Validation, IEC 12207, 62304, ISO 14971, 13485) Experience in medical device development preferred Strong written and verbal communication skills Strong teaching skills Excellent team skills and positive attitude Multi-functional project leadership and/or people management experience  Excellent benefits: in addition to a very competitive salary, we offer a robust benefits package that includes low cost health insurance coverage for you and your family; matching 401(k) as well as a retirement account plan; paid time off (PTO) and holidays. If you believe your education and experience are in line with the position description and qualifications referred to above, and are motivated, energetic, and looking for a new and exciting opportunity, please submit your resume online at the URL below or at www.beckmancoulter.com AN EQUAL OPPORTUNITY EMPLOYER - We believe that the mutual goals of our business and the community can best be met through our policy that consideration of race, color, religion, ancestry, national origin, sex, age, disability, veteran status or other protected characteristics, has no place in the selection, training or promotion of employees. In furtherance of this policy, we have developed a written Affirmative Action program to ensure positive action in providing equal opportunity for employees and applicants. Apply Online: https://recruiter.kenexa.com/bci/cc/CCJobDetailAction.ss?command=CCViewDetail&ccid=bupJEdUjsTs=&job_REQUISITION_NUMBER=70539