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Engineer Jobs in Minnesota

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Job Title: Automation Engineer in Brooklyn Center, MN
Company: Sapphire
Location: Brooklyn Center, MN

Description:
Requisition # :   Assignment Information  Date Submitted :   Positions : 1  Start Date :    End Date :  8/2/2010  Order Status :    Order Type :  Requisition for Contract Labor  CLASS Contact :    OverTime Allowed :   Currency :  -->  Allow receipt of resumes for :    Interview Type :  Interview   Required Travel :  No Travel Required     Work Environment :  Professional   Anticipated Schedule :  Typical 8 Hour/Day  Team Role :   -->  Required Dress Code :  Business Casual   Max resumes to receive :    Contractor Work Location :  Brooklyn Center, MN USA --> Job Description  Labor Category :  Engineering   Job Family :  Manufacturing/Engineering   Job Title :  Manufacturing Process Engineer (Indirect) -- 4 MONTH CONTRACT  Job Duties :  Develops product and process improvements,Performs process and equipment validations ,Utilizes FMEA within process development ,Ensures compliance with GMP’s,Writes engineering and manufacturing specifications  Job Title :  Manufacturing Process Engineer  --> Skill Sets: Required: Desired: Education Level: Undergraduate Degree   High School Diploma or Equivalent PLC Controls: Allen Bradely (A/B) Project Management : Project Coordination   Request Notes :  Need is for an automation engineer. Efforts will involve modification to existing equipment with robotic and PLC control. Candidate will work with internal and external resources to effect modifications and qualify for production use. Sapphire Technologies is an EOE-M/F/V/D and is a wholly owned subsidiary of Randstad Holding nv, a € 17.2 billion global provider of professional employment services and the second largest staffing organization in the world.




Job Title: Quality Assurance Engineer - Infection Prevention Job
Company: 3M
Location: Maplewood, MN

Description:
Quality Assurance Engineer - Infection Prevention-1000206Organization: Health Care BusinessPrimary Location: USA Region-United States-Minnesota-MaplewoodJob Type: ExperiencedDescriptionFor more than 100 years, 3M has been a company that delivers both sustainable growth and consistent results. Today is no exception. We are making great progress toward inventing a new future for 3M - a future of faster growth and increased competitiveness, while continuing to deliver superior results.Medical: Infection PreventionWe offer the broadest array of solutions in the fight against hospital-acquired infections. Our products are backed by a diverse portfolio of educational programs and knowledgeable technical service to provide practical support for your patients and staff.To learn more about this Division go to www.3M.com/infectionprevention.The position of Quality Assurance Engineer located in Maplewood, Minnesota will provide quality leadership and support to Sterilization Assurance Products in the Infection Prevention Division including new product introductions and continuous improvement programs and be responsible for but not limited to the following specific duties:Representing quality on new product development (NPI) projectsValidating test methods, driving reduction in test method variability, and performing cross-over studies.Developing and analyzing shelf life studies to set and validate our product claimsSupporting assigned Sterilization Assurance products, by:Driving CQI (Customer Quality Index) process to improve product quality and process capability.Leading Quality improvement projects to reduce costs and increase customer satisfaction.Evaluating product and process changes for impact on qualityAssuring compliance to internal SOP's and external regulationsAnalyzing customer complaints and trendsLead product risk management activities.The engineer will work and interact significantly with other functions (lab, plant manufacturing, MTD, regulatory, clinical, etc.). He/she will need good written and verbal communication skills, excellent attention to detail, and be process and system oriented. This position can provide a great opportunity to learn, grow, and develop as an employee.QualificationsBasic/Minimum Qualifications: Bachelors Degree A minimum of 1 year microbiology experience.Preferred Qualifications: Bachelor's/Master's degree in Microbiology, Biochemistry, Biology, Chemical Engineering, or related field. Experience with microbiology testing using standard and molecular methods Knowledge of working in a regulated environment for medical devices (i.e. FDA QSR, ISO13485) Previous quality experience Experience in the medical device industry Experience with chemistry and/or biochemistry Strong leadership, decision making, influencing, and analytical skills Effective verbal and written communication skills Extensive experience giving technical presentations to diverse audiences Innovative and resourceful in complex problem solving. Statistical knowledge and practice (Designed Experiments, Sampling Plans, SPC, and ANOVA and Regression) ASQ Certification (e.g. CQE, CQT, etc.) Experience with using Steam and Ethylene Oxide sterilizers Six Sigma Experience, leading Green Belt or Black Belt projects Strong demonstrated leadership ability and the ability to lead teams, identify opportunities for improvement, drive change, and get things doneEmployment StatementApply now for this exciting opportunity with 3M.3M is an equal opportunity employer!




Job Title: Supplier Quality Engineer
Company: CRAY Inc
Location: Saint Paul, MN

Description:
Lead Supply Chain efforts to develop and deploy a supplier Quality Management System for suppliers with hands on approach to high performance computing and storage product mix to include hardware, software, services, IP etc.  Participate and coordinate cross-functional teams promoting and implementing supplier Quality disciplines in Design, Development, Procurement, Manufacturing, Testing and Service. Primary Duties and Responsibilities:• Work with Product Development Core Teams and suppliers to implement consistent quality processes and set high benchmarks for new products from design concept through production.o Implement solutions through collaborative efforts with Product Engineering, Procurement, Planning, QAE’s, Manufacturing, Test and Customer Service. • Development and management of a consistent global Supplier Quality program.o Deploy quality elements throughout the value chain of Make/Buy, RFI and RFP assessments.  o Determine Prime contractor quality flowdown requirements for supply base and assure incorporation of customer requirements in Supply Chain supplier/partner contracts.o Assists in the development, approval, and maintenance of company material specifications, vendor instructions, quality assurance procedures, as well as supplier documents such as Quality Control Plans.• Coordinate quality control processes across supply base. • Identifies and drives continuous quality improvement in area of responsibility.• Develop “8D” disciplines for Failure Analysis from Root Cause to Corrective Action, and critical product escalation process.• Be prepared to lead analysis and resolution to highest impact critical quality control escalations.• Lead efforts on conducting non-conformance reporting and trend analysis to recommend corrective action or process improvement quality of supplier/partner products.o Follows up on corrective actions related to audit findings, nonconforming product, or overall supplier performance to ensure effective resolution and timely closure.• Prioritize supplier/partner quality initiatives based on potential benefits and impact to Cray inc. (efficiency, yield improvement, cost reduction, turn around, customer satisfaction). • Monitor the effectiveness and feedback from corrective actions to ensure that problems have been eliminated (or substantially mitigated). • Collect and analyze data to improve supplier quality and reliability by applying process, statistics and tools and develop and supplier Quality Manual.• Prepare and execute rolling audit plan including system audit, process audit, and follow up audits for continuous improvement.• Analysis of all supplier/partner test results of Cray products.• Assist in incoming sampling/inspection of supplier/partner products.• Works with Supply Chain to track ongoing supplier quality performance and work with suppliers on quality issues.• Works with Supply Chain, Engineering, Manufacturing and Quality Assurance on supplier issues to assure timely acceptance of purchased product.• Conducts or assists in systems/process/product failure mode analysis and initiation of preventive action as it applies to purchase products.• Develops and maintains specifications & SOP's in area of responsibility.• Understands and is able to review quality records to verify information is correct and complete and that specifications have been met.• Create and distribute reports on supplier scorecards, quality performance, supplier corrective action status, containment request status and other reports as determined by management. • Work Supplier development to implement best practices, establish standard work, and eliminate variation and waste to improve performance.o Collects and analyzes supplier quality information from various supplier quality systems and develops reports as needed for senior management review. Provides recommendations based on trendsMinimum Education and/or Experience:• Bachelor degree in Quality, Engineering and/or Materials Science is required, and; • Quality certifications  i.e., ASQ-CQE, Six Sigma, Black-Belt, ISO auditor• 10+ yrs experience in supplier/partner quality assurance and supplier developmentKnowledge, Skills and Abilities:• Understands and can apply quality principles and concepts. • Proficiency with risk analysis tools.• Excellent Organization, written communication and verbal communication at all levels of the organization.  • Leadership and team builder.• Data and Trend analysis.• Previous supplier quality engineering experience with a high technology company.• Knowledge of Microsoft Office Applications.   • Interpretation of engineering drawings and work instructions.  • Desire to help others, learn and assist in a supporting role. • Available and flexible to work when required, including extended hours, night shifts, and weekends, to support Manufacturing & Supply Chain. • Willingness to travel.  • Extended periods of supplier/partner site residency as required. Cray Inc. is an equal opportunity affirmative action employer. If interested, please apply online at http://track.tmpservice.com/ApplyClick.aspx?id Register to View -4172




Job Title: Hardware Quality Engineer Job
Company: 3M
Location: Maplewood, MN

Description:
Hardware Quality Engineer-1000329Organization: Health Care BusinessPrimary Location: USA Region-United States-Minnesota-MaplewoodJob Type: ExperiencedDescriptionAre you ready to grow your career with 3M Food Safety?The position of Hardware Quality Engineer located in Maplewood, Minnesota will be responsible for but not limited to the following specific duties:This QA Engineer will be responsible for: Representing quality and assuring quality on new product development projects Providing complaint analysis, evaluating customer samples and trends, and determining necessary actions to improve quality. Quality Assurance support for assigned Food Safety products. Assessing and validating test methods and performing cross-over studies. Where needed, establish Quality Plans and assist and/or support risk management. Evaluating product and process changes for impact on quality. Leading proactive efforts in product quality and process capability improvement. Assuring compliance to internal SOP's and external regulations. Helping to drive and foster a quality environment/mindset throughout the business The engineer will work and interact significantly with other functions (lab, plant manufacturing, MTD, regulatory, clinical, etc.). He/she will need good written and verbal communication skills, excellent attention to detail, and be process and system oriented. This position can provide a great opportunity to learn, grow, and develop as an employee.QualificationsBasic/Minimum Qualifications: Bachelor's Degree A minimum of three years of electronics hardware experience.Preferred Qualifications: Bachelor degree in mechanical engineering or other related engineering field. Working knowledge of Quality Systems such as ISO 9001 Experienced with molding design and molding operations, DOE, process capability studies and process validation Working knowledge of basis electronics. Experience designing or reliability testing electronic test equipment. Experienced with documentation systems including engineering drawings and change control systems. Skilled communicator, problem solver, supportive team member and balanced risk taker. Strong demonstrated leadership ability and the ability to lead teams, identify opportunities for improvement, drive change, and get things done Knowledge of working in a regulated environment such as ISO 9001 or ISO 13485 Previous quality experience Statistical knowledge and practice (Designed Experiments, Sampling Plans, SPC, ANOVA and Regression, Process and Product Understanding (PPU), and Lean Manufacturing) ASQ Certification (e.g. CQE, CQI, etc.) Ability to multi-task and prioritize Six Sigma Experience, leading Green Belt or Black Belt projectsRelocation: Relocation is NOT authorized for this requisitionAbout 3MFor more than 100 years 3M employees have worked to make people's lives easier and better. Our 79,000 global employees use their ingenuity to invent, manufacture and sell our products in more than 200 countries. These products spring from more than 45 technology platforms that have made us a global leader in major markets and that help us meet real customer needs. In a global, multi-faceted company like 3M, you can explore diverse career opportunities and develop new skills all within one company.About 3M Food Safety Department (Microbiology)The 3M Food Safety Department designs, manufactures and markets a full line of testing an monitoring products globally that assist food processors in providing healthy, wholesome and safe food by managing their quality and safety risk. The 3M Food Safety Department is an exciting growth business, with an excellent brand and quality reputation. In 2006, Food Safety acquired Biotrace International to expand its market presence in this industry.For more information, please visit http://solutions.3m.com/wps/portal/3M/en_US/Microbiology/FoodSafety/Employment StatementApply now for this exciting opportunity with 3M.3M is an equal opportunity employer!




Job Title: Quality Engineer
Company: AGA Medical Corporation
Location: Plymouth, MN

Description:
As a Quality Engineer supporting Product Quality at AGA Medical, your primary focus is to ensure that product performance consistently meets customer requirements.Duties and Responsibilities:• Provide Quality Engineering leadership to manufacturing by maintaining product risk management documents (DFMECA, PFMECA, UFMECA, etc.) throughout the product lifecycle.• Design, implement, and continuously improve component/product/process monitoring methods using SPC where appropriate.• Lead CAPA activities, nonconformance (NCMR) investigations, supplier activities, and complaint investigations for commercialized product ensuring that opportunities are thoroughly addressed and efficiently resolved.• Mistake-proof manufacturing processes to ensure product performance meets pre-determined requirements.• Initiate and/or approve Engineering Change Orders, Validations, and other documents as required.• Design, develop, and validate test methods to evaluate incoming components and finished goods for conformance to specifications.• Perform analysis and identify trends in Quality data, driving improvement actions accordingly.• Update and train others on Quality System and Manufacturing policies and procedures to ensure department efficiency and compliance to regulations.Qualifications:• BS degree in Engineering required, Mechanical Engineering degree preferred.• Lean / Six Sigma Green Belt Certification preferred.• Minimum work experience of 3 years in Process Engineering, Manufacturing Engineering, or Quality Engineering supporting medical device manufacturing.• Knowledge and application of FDA, ISO, and other applicable international regulations.• Knowledge and application of mechanical measurement systems.• Excellent data analysis skills, including understanding of Gage Repeatability and Reliability (Gage R&R).• Exceptional communication skills (technical writing, presentation, and verbal communication skills).• Strong collaboration skills.• Takes initiative, prioritizes, and works efficiently in a dynamic environment. To continue the application process, please visit our booth at the Multicultural Forum’s Virtual Career Fair by clicking on the “Apply now” button.




Job Title: Supplier Quality Engineer_Upward Career Opportunity!!
Company: Byrnes & Rupkey, Inc.
Location: Minneapolis, MN

Description:
Leadership is key!! CQE/CORE, Six Sigma Green Belt+, Black Belt, Lean, Supervisory experience Education: 4-year Engineering degree required. Required skills: · 5+ years of manufacturing and supplier quality experience; · CQE or CORE status desired; · In-depth knowledge of quality management system standards; · Six Sigma Green Belt training required; Black Belt certification desired; · Lean Manufacturing experience desired; · Excellent communication and interpersonal skills; · Skilled in using Ms Office, Access, and PowerPoint. Job Description: This position is with a growing, innovative manufacturing company and will be responsible for improving the supply base and internal quality systems. Duties include: Managing multiple commodity groups for continual performance improvement; Addressing day-to-day quality issues to minimize impact to the production environment; Driving continuous improvement; Using quality skills to continuously drive supplier performance improvements; Guiding and supporting the Quality Technicians on matters related to supplier quality. Please email your resume to Register to View Byrnes & Rupkey, Inc. is an Equal Opportunity / Affirmative Action Recruiting firm.




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