Systems Technology Group Inc. (STG)
Auburn Hills, Michigan
Job Title: Powertrain Supplier Quality Engineer Description: STG is a SEI CMMi Level 5 company with several Fortune 500 and State Government clients. STG has opening for Powertrain Supplier Quality Engineer. This position based in Auburn Hills, MI is for a Fortune 500 client of STG and expected to be long term. STG will provide immigration and permanent residency sponsorship assistance to candidates in the US, if needed. Position Description: The Supplier Quality Engineer will be responsible for managing all aspects of the Advance/Current Supplier Quality functions. The Engineer will provide launch support by providing on-site support at suppliers' facilities to ensure launch readiness as required leading up to and including program launch. Provide on-site support at OEM Assembly plants as required. Work cross-functionally with Engineering, Manufacturing, and Purchasing to ensure proper designs, suppliers, and manufacturing processes are selected. Drive change within both plant manufacturing and component suppliers to resolve component issues. Ensure component suppliers' processes are robust and capable. Lead problem solving activities within internal and external organizations. Manage key component quality milestones. Develop and present program status updates and articulate open issues to senior leadership. Travel will be required to supplier and other OEM locations in the U.S. and Canada (approximately 40%). Requirements: Completed Bachelor of Science in Engineering from an ABET accredited university with 3-5 years commensurate experience in Supplier Quality Engineering, Quality, Production, or Manufacturing. Highly preferred experience with powertrain, engine, transmission systems or casting. Plastic injection or tooling commodities will be considered. Candidates must have proficient supplier engagement experience and communication. • Proven ability to manage multiple projects and tasks • Effective written and verbal communication skills • Proficient interpersonal skills and the ability to work effectively in a cross-functional team • Proficient using Google Suite and Microsoft Office Suite software -Creative problem-solving ability and a results orientation • Comfortable with complex technical analysis -May be required to drive a company car. • Valid driver's license is required as well as a clean driving record. • Will be required to travel internationally to Canada, as well as domestic travel at 40-60% *Preferred Qualifications: Green Belt, Black Belt, or Quality Certification Master's degree Resume Submittal Instruction: Please e-mail a word formatted resume to Suchitra Ray at or contact at In the subject line of the e-mail please include: First and Last Name - Powertrain Supplier Quality Engineer Corporate Information: Established in 1985, Systems Technology Group (STG) is a fast-growing IT consulting and systems integration services firm. STG is a SEI CMMi Level 5 company with expertise in Application Development, Application Management, Web Services (SOA), Data Warehouse, Business Intelligence / Analytics, Wireless Solutions, Legacy migrations and Project Management. STG is proud that clients like Ford Motor Company, Sears Corporation, Chrysler, LLC, Mercedes Benz, United Health, General Motors, State of Texas, State of Michigan, State of Minnesota, State of Georgia, and others trust their IT services needs to STG. STG has offices in North America, Europe and India to service our clients' global IT needs. STG offers a competitive compensation and benefits package including health coverage, vision, dental, life insurance, disability insurance, 401K, paid vacations and paid holidays. For more information about STG, please visit us at . - provided by Dice
Job Title: Powertrain Supplier Quality Engineer Description: STG is a SEI CMMi Level 5 company with several Fortune 500 and State Government clients. STG has opening for Powertrain Supplier Quality Engineer. This position based in Auburn Hills, MI is for a Fortune 500 client of STG and expected to be long term. STG will provide immigration and permanent residency sponsorship assistance to candidates in the US, if needed. Position Description: The Supplier Quality Engineer will be responsible for managing all aspects of the Advance/Current Supplier Quality functions. The Engineer will provide launch support by providing on-site support at suppliers' facilities to ensure launch readiness as required leading up to and including program launch. Provide on-site support at OEM Assembly plants as required. Work cross-functionally with Engineering, Manufacturing, and Purchasing to ensure proper designs, suppliers, and manufacturing processes are selected. Drive change within both plant manufacturing and component suppliers to resolve component issues. Ensure component suppliers' processes are robust and capable. Lead problem solving activities within internal and external organizations. Manage key component quality milestones. Develop and present program status updates and articulate open issues to senior leadership. Travel will be required to supplier and other OEM locations in the U.S. and Canada (approximately 40%). Requirements: Completed Bachelor of Science in Engineering from an ABET accredited university with 3-5 years commensurate experience in Supplier Quality Engineering, Quality, Production, or Manufacturing. Highly preferred experience with powertrain, engine, transmission systems or casting. Plastic injection or tooling commodities will be considered. Candidates must have proficient supplier engagement experience and communication. • Proven ability to manage multiple projects and tasks • Effective written and verbal communication skills • Proficient interpersonal skills and the ability to work effectively in a cross-functional team • Proficient using Google Suite and Microsoft Office Suite software -Creative problem-solving ability and a results orientation • Comfortable with complex technical analysis -May be required to drive a company car. • Valid driver's license is required as well as a clean driving record. • Will be required to travel internationally to Canada, as well as domestic travel at 40-60% *Preferred Qualifications: Green Belt, Black Belt, or Quality Certification Master's degree Resume Submittal Instruction: Please e-mail a word formatted resume to Suchitra Ray at or contact at In the subject line of the e-mail please include: First and Last Name - Powertrain Supplier Quality Engineer Corporate Information: Established in 1985, Systems Technology Group (STG) is a fast-growing IT consulting and systems integration services firm. STG is a SEI CMMi Level 5 company with expertise in Application Development, Application Management, Web Services (SOA), Data Warehouse, Business Intelligence / Analytics, Wireless Solutions, Legacy migrations and Project Management. STG is proud that clients like Ford Motor Company, Sears Corporation, Chrysler, LLC, Mercedes Benz, United Health, General Motors, State of Texas, State of Michigan, State of Minnesota, State of Georgia, and others trust their IT services needs to STG. STG has offices in North America, Europe and India to service our clients' global IT needs. STG offers a competitive compensation and benefits package including health coverage, vision, dental, life insurance, disability insurance, 401K, paid vacations and paid holidays. For more information about STG, please visit us at . - provided by Dice
Teleflex
Morrisville, North Carolina
Position Summary The Senior Development and Sustaining Engineer is responsible for the development and maintenance of respiratory, anesthesia, and/or urological products. Under minimal direction, the incumbent will organize and manage multiple projects and ensure they are completed in a timely manner, create design ideas for new products, and develop creative solutions to existing products when problems arise or modifications are requested. Principal Responsibilities Conduct research and/or development projects associated with the design and/or modification of medical devices, components, models, or mechanisms. Prepare or coordinate formal documentation of the product designs, risk analysis, product specifications, market specifications, etc. according to established product development procedures. Initiate formal reviews to get approvals per procedures. Develop, maintain and publish product development plans for assigned projects with critical milestones and timelines. Develop and coordinate the running protocols for the validations of new or modified devices or components, including validations of the design, manufacturing process, assembly, packaging, and sterilization where applicable. Investigate and resolve technical problems involving product performance, production equipment, or facility systems affecting production. Coordinate the product design and development process with appropriate support departments such as engineering, regulatory, documentation, tooling, and manufacturing. Serve as project leader for assigned projects and follow up on all aspects of projects, including conducting reviews with support groups and outside resources where applicable. Prepare or follow up on preparation of design drawings, specifications, estimates of costs, mainframe updates, etc. Discuss and consult with sales staff or customer on product requirements and specifications where design or manufacturing problems are involved. Work with manufacturing in the justification and the selection of the manufacturing process. Assign projects and establish priorities to ensure datelines and goals are achieved. Develop assembly methods and procedures. Create engineering draws and specifications. Coordinate changes in process, tolling, and equipment identified to positively impact the manufacturing process, while staying within GMP guidelines. Coordinate the reporting on project status for all responsible projects. Direct reports in formal periodic project review meetings, to include cost reduction progress, capital spending, and expense status. Enhance personal growth and development through participation in education programs, current literature, training meetings and workshops. Participate actively in continuous quality improvement activities through compliance with safety standards. Demonstrate professional responsibilities by cooperating with other personnel to achieve department and interdepartmental goals and objectives and maintain good employee relations. Organize, evaluate, and coordinate engineering studies with professional, technical, and clerical staff of a product evaluation department. Analyze complex, technical and administrative problems and adopt an effective course of action. Conduct comprehensive studies and preparation of reports including recommendations. Make effective presentations to, and participate in, a variety of meetings and conferences with other companies and the public. Prepare clear and concise statements and reports. Education / Experience Requirements Bachelor s degree in Biomedical Engineering or closely related field. Possession of BS degree may be substituted for six (6) additional years of work experience in the design and/or modification of plastic components for the medical industry 5+ years experience in product development 3+ years experience leading medical device engineering projects Experience with injection molding, plastic extrusion and plastic part assembly process and methods required Experience with CAD (design/drafting) programs, including SolidWorks, preferred Specialized Skills / Other Requirements Solid understanding of and experience with: U.S. FDA GMP and ISO requirements for the design, validation, manufacturing processes, secondary operations and assembly of medical components and devices. ISO and ASTM testing methods for medical devices and general plastic components Principles and practices of professional engineering. Regulations pertaining to medical device design and design modifications. Demonstrated creativity and ingenuity in applying engineering principles and practices and drawing solutions from a wide range of experience. Effective written and oral communication skills and ability to present information to, and respond to questions from, various audiences. Ability to interpret and follow instructions furnished in written, oral, diagram, or schedule form. Intermediate knowledge of Microsoft Office Suite (Project, Word, Excel, and Access) Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Proven ability to establish and maintain effective working relationships with peers. Working Conditions / Physical Demands Typical research lab and office environment; occasional work in manufacturing areas and some field work. Some exposure to the electrical/mechanical/power manufacturing or testing equipment, with occasional heat and noise exposure and exposure to dust. May visit domestic and international (Mexico, Asia) manufacturing sites. Travel required up to 10%. Associated topics: boiler, catia, mechanical, mechanism, motor, powertrain, proe, rotordynamic, turbine, vibration
Position Summary The Senior Development and Sustaining Engineer is responsible for the development and maintenance of respiratory, anesthesia, and/or urological products. Under minimal direction, the incumbent will organize and manage multiple projects and ensure they are completed in a timely manner, create design ideas for new products, and develop creative solutions to existing products when problems arise or modifications are requested. Principal Responsibilities Conduct research and/or development projects associated with the design and/or modification of medical devices, components, models, or mechanisms. Prepare or coordinate formal documentation of the product designs, risk analysis, product specifications, market specifications, etc. according to established product development procedures. Initiate formal reviews to get approvals per procedures. Develop, maintain and publish product development plans for assigned projects with critical milestones and timelines. Develop and coordinate the running protocols for the validations of new or modified devices or components, including validations of the design, manufacturing process, assembly, packaging, and sterilization where applicable. Investigate and resolve technical problems involving product performance, production equipment, or facility systems affecting production. Coordinate the product design and development process with appropriate support departments such as engineering, regulatory, documentation, tooling, and manufacturing. Serve as project leader for assigned projects and follow up on all aspects of projects, including conducting reviews with support groups and outside resources where applicable. Prepare or follow up on preparation of design drawings, specifications, estimates of costs, mainframe updates, etc. Discuss and consult with sales staff or customer on product requirements and specifications where design or manufacturing problems are involved. Work with manufacturing in the justification and the selection of the manufacturing process. Assign projects and establish priorities to ensure datelines and goals are achieved. Develop assembly methods and procedures. Create engineering draws and specifications. Coordinate changes in process, tolling, and equipment identified to positively impact the manufacturing process, while staying within GMP guidelines. Coordinate the reporting on project status for all responsible projects. Direct reports in formal periodic project review meetings, to include cost reduction progress, capital spending, and expense status. Enhance personal growth and development through participation in education programs, current literature, training meetings and workshops. Participate actively in continuous quality improvement activities through compliance with safety standards. Demonstrate professional responsibilities by cooperating with other personnel to achieve department and interdepartmental goals and objectives and maintain good employee relations. Organize, evaluate, and coordinate engineering studies with professional, technical, and clerical staff of a product evaluation department. Analyze complex, technical and administrative problems and adopt an effective course of action. Conduct comprehensive studies and preparation of reports including recommendations. Make effective presentations to, and participate in, a variety of meetings and conferences with other companies and the public. Prepare clear and concise statements and reports. Education / Experience Requirements Bachelor s degree in Biomedical Engineering or closely related field. Possession of BS degree may be substituted for six (6) additional years of work experience in the design and/or modification of plastic components for the medical industry 5+ years experience in product development 3+ years experience leading medical device engineering projects Experience with injection molding, plastic extrusion and plastic part assembly process and methods required Experience with CAD (design/drafting) programs, including SolidWorks, preferred Specialized Skills / Other Requirements Solid understanding of and experience with: U.S. FDA GMP and ISO requirements for the design, validation, manufacturing processes, secondary operations and assembly of medical components and devices. ISO and ASTM testing methods for medical devices and general plastic components Principles and practices of professional engineering. Regulations pertaining to medical device design and design modifications. Demonstrated creativity and ingenuity in applying engineering principles and practices and drawing solutions from a wide range of experience. Effective written and oral communication skills and ability to present information to, and respond to questions from, various audiences. Ability to interpret and follow instructions furnished in written, oral, diagram, or schedule form. Intermediate knowledge of Microsoft Office Suite (Project, Word, Excel, and Access) Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Proven ability to establish and maintain effective working relationships with peers. Working Conditions / Physical Demands Typical research lab and office environment; occasional work in manufacturing areas and some field work. Some exposure to the electrical/mechanical/power manufacturing or testing equipment, with occasional heat and noise exposure and exposure to dust. May visit domestic and international (Mexico, Asia) manufacturing sites. Travel required up to 10%. Associated topics: boiler, catia, mechanical, mechanism, motor, powertrain, proe, rotordynamic, turbine, vibration