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Quality Control Engineer Jobs
Search all 4,515 QA Jobs for Quality Control Engineer Jobs|
Job Title: Quality Engineer
Company: Katecho, Inc. Location: Des Moines, IA Description: Katecho, Inc. an OEM manufacturer founded in 1984 is strategically located in America’s heartland - Des Moines, Iowa. Katecho employs approximately 260 employees and manufacturers a variety of medical products specializing in disposable electrodes for pacing, defibrillation, muscle stimulation, patient monitoring, and electro-surgical. Katecho, Inc. also designs and produces conductive adhesive hydrogels. Katecho is more than just a manufacturer, as the company offers: engineering design services, product testing and verification, regulatory support, and inventory management. From initial product concept to final package, we employ multi-disciplined machine operators to engineers and support staff members who add value to our bottom line. In addition, we offer careers in our highly visible and extensive laboratory facilities which are capable of performing a wide range of mechanical, electrical and environmental testing. “Our commitment to quality never ends” so please join our Quality Department for rewarding positions. Great Career Opportunities Quality Engineer
Qualifications needed to be considered for this opportunity are: BA in Engineering with 3-5 years experience in quality. ISO9001:2000, 13485:2003 FDA preferred. ASO Quality Engineer Certified or within one year of employment. Katecho, Inc offers a competitive salary, 401 (K) Match plus full benefits. Apply today!
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Job Title: Supplier Quality Engineer
Company: See Job Description Location: Ville Platte, LA Description: Cameron (NYSE:CAM) is a leading provider of flow equipment products, systems and services to worldwide oil, gas and process industries. Leveraging its global manufacturing, sales and service network, Cameron's 10 operating divisions work with drilling contactors, oil & gas producers, pipeline operators, refiners and other process owners to control, direct, adjust, process, measure and compress pressures and flows. The company generates annual bookings in excess of $4 billion with more than 12,500 employees and is headquartered in Houston, Texas. Along with a competitive salary Cameron offers attractive benefits, including: Medical * Dental * Vision * Life Insurance * 401K Investment Plan * Profit Sharing Plan * Pension Plan * Flexible Spending Accounts * Education Reimbursement * Long-Term Disability * Short-Term Disability * Paid Holidays * Relocation Benefits (where applicable)Responsibilities include creating supplier development quality plans, improving and measuring supplier quality performance, and support product/process improvement initiatives. General responsibilities are as follows: • Leads the effort in creating and implementing supplier development quality plans. • Demonstrates leadership in a team environment resulting in continuous improvement achievements. • Manages the Supplier Corrective Action process to ensure effective, efficient and timely corrective actions are implemented. • Required to interact with suppliers, management at all on quality related concerns from the supply base effecting product compliance, corrective and preventative actions. • Directs the qualification and surveying of new suppliers. • Leads on-site audits, surveys when supplier performance indicates need for corrective action. • Facilitate communication between the Business (Marketing), Engineering Teams and the supply base regarding product requirements, technical discussions and failure analysis. • Works with Engineering, Manufacturing and Suppliers in defining and standardizing inspection criteria resulting in inspection specification. • Prepares monthly, quarterly summaries of supplier performance data and improvement activities. • Technical lead and contact on outsourcing of turnkey products currently or previously made in house. • Assist with team member training • Promote and utilize six sigma methodology • Other essential duties as directed. • Bachelor’s degree in Mechanical or Industrial Engineering for Engineering Designation; or • Bachelor's degree in Industial Technology or equivalent experience for Specialist Designation. Required Skills & Experience • 3+ years related manufacturing experience • Project Management experience • Experience in working closely with Marketing, Supply Chain, R&D and Manufacturing to develop practical solutions to complex problems. Preferred Skills & Experience: • Working knowledge of oil-field pipeline regulations and standards preferred. • Detailed understanding of a commodity group such as Forgings, Castings, Machine Components, Purchased Parts/ Services. • Low-cost country experience. • Formal Lean or Lean Six Sigma training and certification preferred. Additional Skills and Knowledge: • Strong writing and presentation skills, have ability to read and interpret Quality System documents, Engineering drawings and work instructions. • Ability to develop, update quality management system processes and work instructions. • Proficient in MS office suite (Word, Excel, PowerPoint). • Familiar with non-compliance trending statistic analysis methodology and tools. • Travel both domestic and international. • Work well with minimal supervision and have ability to manage multiple tasks effectively. • Ability to stay focused and perform required duties in a very fast paced work environment. |
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Job Title: Quality Control Engineer
Company: DP Technology Corp. Location: Camarillo, CA Description: Quality Control Engineer DP Technology is looking for a creative problem solver to take responsibility for a software quality control system. This is an opportunity to use your practical expertise to initiate a product quality control program including the creation, implementation and execution of the testing protocols. While responding to a fast-paced environment the successful candidate will use analytical, creative and critical thinking skills to design and maintain both the manual and automated quality systems. This position will work with our Product Managers and Software Engineers to assess the various functional and design specifications needed to create the necessary test plans and tools. You will also work in partnership with the Software Engineering and Product Management teams to deliver on-time results. This position will tap into your strong attention to detail as you develop and report the project and product level results of your quality program. If you have the initiative and drive to put your imaginative problem-solving skills to good use, submit your resume and salary history to the email address in this ad. DP Technology is a computer-aided manufacturing ( CAM ) software market leader with a mission to provide CNC programmers with the most powerful CAM software ever. DP Technology's flagship product, ESPRIT, captures the company's vision of technology's potential and its passion for excellence. DP Technology maintains its worldwide headquarters and product development team in Camarillo , California , with sales and support operations in Europe , Asia , and North and South America . For additional information about DP Technology and ESPRIT visit the company web site at http://www.dptechnology.com/ . Qualifications : · BS Computer Science or equivalent technical degree · 2 – 4 years of formal software quality assurance testing · Skilled in system analysis · Requires an inquisitive mind and a strong drive to push the limits · Must be a problem solver |
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Job Title: Quality Control Engineer - Automotive Parts
Company: Location: Chicago, IL Description: Quality Control Engineer Use your Quality background at an Automotive Parts Supplier! Are you excited for the opportunity to travel overseas? Our client is a Japanese owned company that is seeking a Quality Control Engineer who can oversee keeping the facility in line with regulations. Requirements We are very interested in talking to candidates with the following qualifications: At least 1 year of Quality experience in the automotive industry Knowledge of ISO regulations Ability to prepare departments for governmental and corporate inspections Ability to travel overseas to visit customers and company facilities Benefits Full Benefits Package 401K Candidates must be legally authorized to work in the United States. Every day, we receive hundreds, and sometimes thousands, of resumes. As we seek to create a mutually beneficial match between you, the applicant, and your potential employer, we rely on you to provide us with information that is precisely related to our posting. If you can provide this information, we can guarantee you the maximum amount of consideration concerning this opportunity. MRJapanese is an International Top 50 office within the world’s largest recruiting network! Our recruiters have direct work experience in your industry, and we want to make sure you find a rewarding new chapter in your professional career! Please visit www.mrjapanese.com and view all our currently available jobs. |
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Job Title: Quality Control Engineer
Company: CAI Personell Location: Nashville, TN Description: Quality Control Engineer – Automotive Responsible: for supporting manufacturing of Plastic Injected and Electronic parts and products for the Automotive industry. Insure that quality products are produce for Automotive Customers, that QS9000 and TS16949 Quality Standards are met. Requirements: are BS Engineering degree, 1 to 5 years of QC Engineering experience in production of Plastic Injected and Electronic assembled products. Skilled in use of QS9000 and TS16949 in fabrication and welding. Compensation: in the $42,000 to 57,000 range, based on qualifications and experience. Submit resume as an MS Word document to Register to View |
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Job Title: Senior Manufacturing Process and Quality Control Engineer
Company: Location: Boston, MA Description: OVERVIEW: The Kensho Group has been retained by our client to conduct a confidential search for their Senior Manufacturing Process and Quality Control Engineer . The position is based in the suburban Boston, MA area. This dynamic, publicly traded Medical Device company is a true leader in the field of high powered laser based medical devices for aesthetic applications. RESPONSIBILITIES: Existing Contract Manufacturing Relationships - Lead continuous improvement through regularly scheduled assessments and closed loop corrective action implementation - In conjunction with BSC quality, respond efficiently and effectively to address product quality issues - Initiate and manage supplier CAPAs to successful closure - Monitor and drive suppliers to improve quality metrics via effective process changes - Identify and control critical processes - Assist suppliers and Candela teams with complaint investigations and C/A - Manage outsourcing of sub-assemblies to Candela suppliers New Business - Aid new business development teams in supplier assessments to ensure selection of partners that can deliver consistently high quality products. |
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Job Title: MANUFACTURING POSITONS
Company: STAFFING SOURCE, INC Location: Old Saybrook, CT Description: L;BL_staffing_source MANUFACTURING Our client located in the Groton and Old Saybrook areas have immediate needs for the following: * Welders- 1st & 2nd shifts * Electronic Field Tech- 60% travel * CNC Programmer * CNC Punch-set-up/op * Mechanical Assembler * Manual Machinist * Maint Mech- 2nd shift * X-Ray Tech-mfg * Sandblaster * QC Engineer * Mechanical Engineer- Biomed Send resume to oldsaybrook Register to View or call Register to View for interview. |
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Job Title: Quality Control Engineer
Company: Brown-Forman Corporation Location: Lynchburg, TN Description: COMPANY: Brown-Forman Corporation is an independent, publicly-traded producer and marketer of premium spirits, wines, and other adult beverages, including Jack Daniel’s Tennessee Whiskey, Finlandia Vodka, Southern Comfort, Fetzer Vineyard California Wines, Korbel California Champagnes, Sonoma-Cutrer Estate Bottled Wines, Tuaca, Chambord, and, Herradura and el Jimador Tequila . For more information about Brown-Forman and our brands, please visit our website at www.brown-forman.com . Job Description: Basic Function Responsible for monitoring quality and adherence to specification all raw materials and finished goods, as well as collecting and reporting production and process information to management. Assist and advise operating areas in regard to maturation, processing, testing and use of quality tools. In Manager’s absence, assumes responsibility for departmental activities. Responsibilities Collects data, performs statistical analysis, and reports trends related to materials and finished goods. Provides reports and recommendations to plant and corporate management. Initiates and/or manages corrective and preventive actions as required to improve package quality. Oversees the collection of quality data related to materials and finished goods. Analyzes data and prepares reports with recommendations to plant and corporate management. Coordinates with Purchasing to maintain open communication with vendors to meet the specifications of purchase orders. Document feedback to vendors and require corrective action from vendor to ensure high quality packaging materials. Assumes duties of all QC Specialists and QC Technical Consultant during absences to insure that there is no disruption in delivery of QC services to the plant. Assists Bottling and Bottling Maintenance in resolving process and operational issues as they relate to quality. Coordinates investigation of complaints and initiates any corrective action necessary to prevent reoccurrence. Identify, report and assist operations personnel in addressing processing and production problems related to product quality. Select and manage external resources as needed to complete analyses to ensure high quality processes and materials are used during all areas of production. Assist Sr. QC Specialist with management of ISO 9001 compliance for Jack Daniel, Prop. Shared responsibility for developing, maintaining and controlling documented ISO 9001 Quality System. Directs and oversees Inc. and Prop. salaried QC staff in regards to meeting personal commitments. Provide leadership for the sitewide continuous improvement effort. Insure appropriate quality training is provided for all employees. Manage the North QC hourly employees, including the QC lab, still lab, mellowing building, and cistern room. Insure uninterrupted QC services to support distillery production schedule. Create annual budget and insure adherence to spending annual plan. Must Requirements Bachelor’s degree in Science or related field, plus 5-7 years experience in manufacturing, packaging, and quality. Demonstrated ability to apply comprehensive knowledge of analytical procedures and quality control tools to the completion of complex assignments. Strong skills in math and statistics; understanding of Statistical Process Control and apply to manufacturing environment. Strong computer skills including Word and Excel. Demonstrated communication skills—ability to clearly communicate technical issues to all levels of employees. Demonstrated project leadership and interpersonal skills with ability to coordinate efforts with JD production, vendors and Corporate. Knowledge of ISO-9001:2000 standard. Demonstrated Managerial experience – 3 – 5 years of direct management of personnel. Preferred Requirements Graduate degree in chemistry, engineering, or related field. Experience in the food and beverage industry. Professional certifications related to quality control, quality systems, and analytical chemistry. Knowledge of SAP software for inventory control and quality management. Knowledge of BATF regulations as they apply to distilled spirits. TO APPLY: Please visit us at http://www.brown-forman.com/careers/ Please look for "QC Engineer” or for the requisition # "1127BR” in the keyword search field. |
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Job Title: Quality Control Engineer - Medical Devices
Company: Confidential Location: Cambridge, MA Description: Growing medical robotics manufacturer seeks experienced Quality Control engineer for overseeing continued product quality -- in mechanical and electrical systems -- during production ramp-up. Duties: - Solid familiarity with ISO 13485, or similar, quality management system and related recordkeeping. - In-process and final acceptance inspection, including verifying mechanical tolerances, electrical functioning, and system performance prior to release. - Perform equipment calibration. - Read schematic drawings. - MS Excel and Word. Desirable: Write software programs for quality testing. The ideal candidate is comfortable in a small start-up environment, enjoys hands-on as well as project-planning responsibilities, and is excited to help execute a rapid growth strategy. |
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Job Title: Product Quality Control Engineer
Company: KimberlyClark Location: Fullerton, CA Description: At Kimberly Clark, we believe in recruiting the best people and putting them in the right jobs so that they can do their best work. We are a global health and hygiene leader, and our trusted brands are an indispensable part of life for 1.3 billion people in more than 150 countries. To maintain this trust and pioneer new product categories, we're seeking people who share our passion for excellence, teamwork and original thinking. Join our team to provide a variety of functions associated with product production and manufacturing. Monitors process equipment requirements and set-up, ensuring that all equipment used is compatible with the specific process. Ensures that processes, tools, products and materials meet established quality standards and requirements. Monitors use of and maintains inventory of necessary raw materials. Serves as liason between operations managers and leadership. Bachelor's degree and three to five years of experience required. Click here to apply via the Kimberly Clark Career Opportunity Portal Minimum Education Required: Bachelor Years of Experience Required: 3-5 Years Expected Travel Time: About 25% This company may offer relocation assistance. |
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