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Quality Assurance Technician Jobs
Search all 4,515 QA Jobs for Quality Assurance Technician Jobs|
Job Title: Senior Quality Technician
Company: New Berlin Plastics Location: New Berlin, WI Description: Job Summary: Responsible for leading the effort to understand customer requirements by qualifying the product/process and translating them into effective process controls. Drive continuous improvement by working closely with Director of QA & Continuous Improvement. Duties and Responsibilities:
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Job Title: QA Lead Auditor
Company: Administaff Location: Orlando, FL Description: Global Quality Assurance, Inc. (GQA) is the preferred provider of audit, surveillance and related quality program services to the nuclear power industry and its suppliers. Headquartered in Orlando, Florida, we are led by a management team with more than 30 years industry related experience and is recognized internationally as a leader in the field. Global Quality Assurance, Inc. provides the skilled manpower to perform independent quality system assessments, internal and supplier audits, quality program development to satisfy 10CFR50, NQA and ISO, source surveillance/witness inspections of supplier activities, commercial grade item surveys, 10CFR50 Appendix B and NQA Nuclear audits. GQA also provides both consulting for program improvements and process enhancements as well as formal training courses on Commercial Grade Dedication, Auditor Training, ASME/NQA1 and Root Cause Analysis. Quality Assurance (QA) Lead Auditor – Nuclear While reporting directly to and is fully accountable to the Quality Assurance Manager, the QA Lead Auditor will perform independent audits in various areas of client organizations (e.g. Engineering, Operations, Maintenance, Work Management and support organizations) for our clients with nuclear quality programs, including the audit, survey or surveillance of client supplier/vendor/contractor QA/QC programs to ensure compliance. In this role, you will review documents, witness the performance of audited activities, prepare checklists and agendas for audit, as well as perform audits and assessments of performance, conduct pre and post-audit meetings/interviews and prepare final audit reports in a timely manner (GQA standard of 15 days). The QA Lead Auditor will ensure and document the corrective actions are taken based on report findings. As assigned, you will review client organization’s QA manual and implementation procedures to verify compliance with industry codes and standards, NRC regulations and regulatory commitments, in conjunction with analyze findings/issues/non-conformances identified during audits to determine program quality and identify performance trends. Other Key Responsibilities:• Maintain up-to-date knowledge and understanding of NRC revisions to regulations and industry codes and standards, including maintaining qualifications needed for Lead Auditor certification per ANSI N45, 2.23 and NQ A1 • Assist the various project functions for the implementation of QA requirements up to and including site QA/QC Project Management • Provide other related consulting services as needed to support client needs and expectations • Ensure that all assigned clients receive the highest levels of service and support consistent with the goals and objectives set forth by the President and specified in the company’s mission statement Qualifications: The ideal candidate will possess a High School diploma or equivalent with 1+ years documented experience in Nuclear Operations or any phase of a nuclear facility’s operations. Working knowledge and experience in 10CFR50 - Appendix B QA requirements, ASME NQA-1 standards audit performance, audit techniques and related technical expertise essential. Basic understanding of process improvement and procedure writing and ability to perform independently to specific criteria, to analyze results, to communicate issues, to consult and provide recommendations required. Other Requirements: • General knowledge of electrical and mechanical fabrication, refurbishment and repair practices • Ability to validate and accurately analyze information and then to make and document sound decisions that have considerable business impact • Strong communication skills in the English language • Ability to communicate effectively and collaborate with clients, peers, engineering staff, management and vendors at all organizational levels in to successfully meet shifting needs • Ability to question the status quo and be comfortable with being challenged • Ability to adapt and respond effectively to new or changing conditions • Ability to identify, document and provide corrective recommendations for root cause issues VS symptoms • Experience in balancing the requirements of and prioritizing the activities associated with the successful execution of multiple projects, including ability to consistently meet multiple critical deadlines to meet client and GQA requirements • Proficiency in Microsoft Office applications (E.G. Excel, Word, etc.) • Valid driver’s license with a driving record that will allow coverage under company insurance policies • Successful completion of a 5 year minimum background and fitness of duty compliance check as required to work in this position in the nuclear industry • Experience in quality management system design, development and implementation preferred • Qualified Lead Auditor to ANSI N45.2.23/NQA1 preferred • 2+ years working with nuclear quality requirements preferred • Experience with ASME and IEEE standard application preferred • Associate’s or Bachelor’s degree from an accredited institution with a concentration in Engineering or a technical curriculum, as well as professional licensure preferred • Multilingual proficiency both oral and written preferred Benefits: We value our employees’ time and efforts. Our commitment to your success is enhanced by our extensive benefits package including paid time off, medical, dental and vision benefits and future growth opportunities within the company. Plus, we work to maintain the best possible environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where each person feels encouraged to contribute to our processes, decisions, planning and culture. To Apply: To respond to this opportunity, please go to: http://www.MyChoiceEngine.com/Role/45846 Administaff is not a staffing agency. In fact, most of our listings presented are great full-time or part-time opportunities with small- to medium-sized companies. By delivering HR services such as recruiting, payroll and training, Administaff can help its clients focus on what they do best. And because we have the inside track to these firms, you'll have a jump on your next career! Administaff is proud to be recognized: Most Admired Companies, Fortune 1999, 2000, 2001 and 2002, Fortune 500, Platinum 400 and Forbes. EOE |
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Job Title: Quality Assurance Technician
Company: Weatherchem Corporation Location: Twinsburg, OH Description: Weatherchem Corporation is a privately-owned plastics packaging manufacturer serving a variety of niche markets. Our mission is to be the recognized leader in designing, developing, and delivering convenient, controlled, dispensing solutions for leading consumer packaged goods companies. Weatherchem is an entrepreneurial organization valuing integrity, learning, creativity, a passion for excellence, safety and fun! Job responsibilities include : (all duties are to be performed within a continuous improvement and team mindset) Investigate and resolve product quality and customer complaints using 8Ds, 5 Phase 5 Why, etc. Analyze test data to measure reliability. Collect and analyze quality metrics and statistical data. Identify quality improvement opportunities. Review sampling and inspection plans for statistical significance. Establish SPC programs, as appropriate. Write ISO 9001/2000 specifications, as required. Assist in the development of standards for inspection, testing and evaluation of manufacturing processes. Minimum Certification and Education CQT or CQA required Associate’s degree in a Science related field Minimum Previous Experience Required 3 years in a fast paced manufacturing environment, preferably in plastic injection molding Skills Basic knowledge of statistics, SPC and process capability concepts Excellent verbal and written communication Advanced computer literacy Good reading comprehension Good mathematical skills Weatherchem offers a comprehensive benefits package including medical, dental, prescription, vision, disability, vacation, tuition reimbursement, 401(k), profit sharing retirement. Visit our website at www.weatherchem.com to learn more about us. EOE |
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Job Title: QC/QA Laboratory Technician
Company: Location: Newark, DE Description: Is it time for you to move on to an exciting, growing company? Then Kelly Scientific Resources has the job for you! KSR is seeking an experienced scientist to work on a temporary assignment as a QC/QA Lab Technician in Newark, DE. The ideal candidate would have experience in QC/QA, using measuring devices (steel rulers, calipers, micrometers, etc) and performing material property tests. Experience in calibrations and/or auditing is a plus as well as experience with PPAP. Strong mathematic and computer skills are required. Some college or related work experience needed. This position won't be available for long so APPLY TODAY! |
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Job Title: QA Technician
Company: Location: Louisville, CO Description: QA Technician Description: Seeking an Electrical Mechanical Technician responsible for completion of quality inspection activities including receiving, inspection of purchased components and assemblies in accordance with inspection standards and engineering drawings, using measuring equipment. Requirements: Minimum of 3 years electrical and mechanical inspection experience, working with calibrated equipment in the medical industry. Working knowledge of quality system standards / regulations (such as ISO 9000, ISO 13485 and/or FDA Quality System Regulation. Able to use basic mechanical measurement tools, including but not limited to calipers, micrometers, pin gage, go/no gage, height gage, and surface plate. " Experience in medical device industry " ASQ Quality Technician certification. " Able to read engineering drawing and specifications. " Able to apply sampling plans. " Literate in MS Word and MS Excel. " High school diploma " High level of attention to detail. " High level of communication skills " Experience in working independently in a team environment. " Enthusiastic attitude " Open to learning new skills and taking on new responsibilities Volt is an equal opportunity employer. Location: Louisville, CO Type: CONTRACT Duration: Temp to Hire Pay Rate: $15.00 - $20.00 Hourly DOE Contact: Volt Technical Resources Register to View Volt Services Group 4430 Arapahoe Ave., Ste. 100 Boulder, CO 80303 PH: Register to View FX: Register to View |
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Job Title: Quality Assurance Technician
Company: Location: Bordentown, NJ Description: Reporting to the Quality Assurance Manager/Supervisor the Quality Assurance Technician is responsible for providing food safety, quality testing and review to insure that production safety/quality and standards are being achieved. Trains and supports manufacturing personnel in quality systems to maximize product quality. Initiates problem solving activities relating to quality parameter and food safety. Assist in preparing the plant for third party audits as well as regulatory and GMP audits. Perform other miscellaneous duties/projects as assigned. A successful candidate will have a minimum of o 2-4 years of related experience in quality techniques. Good communication skills, which includes verbal and written communications. Must have strong computer skills, specifically in Excel, WMS, SAP or other systems that will perform Code Trace, Lot trace and review consumer complaints. Requires general knowledge of simple chemical testing, such as acid/base titrations, pH meters, spectrophotometer, refractometer, food safety, GMP/food hygiene and thermal process. |
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Job Title: Sr.QA Technician - (Job Number: 0804545)
Company: Location: Warren, NJ Description: Cordis Corporation, a member of Johnson && Johnson&'s Family of Companies is recruiting for a Sr. QA Technician, located in Warren, NJ. Ground breaking, life changing careers that reward the power of ideas and innovation. For more than 40 years, Cordis Corporation has pioneered less invasive treatments for vascular disease. Technological innovation and a deep understanding of the medical marketplace and the needs of patients have made Cordis the world's leading developer and manufacturer of breakthrough products for interventional medicine, minimally invasive computer-based imaging, and electrophysiology. Today, over 7,000 Cordis employees worldwide share a strong commitment to continue the Company's groundbreaking work in the fight against vascular disease. Cordis Corporation offers tremendous opportunities and world-class resources. Our decentralized structure provides the feel of a small-company environment with big-company impact. We are focused on developing leaders with a broad base of business and cultural skills, along with a strong commitment to the values expressed in Our Credo. By choosing Cordis Corporation, you are choosing to positively impact the lives of millions of people each year. The Sr. QA Technician under limited supervision, performs and documents moderately complex technical functions relating to test, quality control, lay'out, fabrication, modification and assembly of mechanical equipment and/or components. Performs electrical, mechanical, electromechanical, developmental or test technician duties in such areas as manufacturing, maintenance, quality, testing, engineering, where some judgment is required. Constructs, inspects, calibrates, adjusts, tests and maintains equipment, components, devices and systems. Summary reports, analysis of technical data, evaluation of quality control data and instrument troubleshooting are fully within the scope of this position. Utilizes a wide variety of developmental/manufacturing tests or diagnostic test equipment to check out, test, trouble shoot and maintain tools components, instruments, test apparatus and associated specific discipline equipment. May assist more senior technicians and engineers in specific discipline. Performs and documents moderately complex operational functional testing, troubleshooting and debugging of components, subassemblies, materials and manufacturing systems to isolate faults and determine remedy for malfunctions. Writes moderately complex technical reports and develops charts, graphs, and schematics to describe and illustrate systems/tests operating characteristics, malfunctions, deviations from design specifications, and functional limitations. Troubleshoots electrical, test, mechanical, facilities or hydraulic systems, components, and equipment. May provide guidance to lower level technicians. Performs moderately complex process/product tests and audits for conformity to quality and/or regulatory requirements. Performs self'inspections of own work. When applicable, follows standard operating procedures for all tasks. AA or equivalent; or trade/technical schooling; and 5-9 years of related experience and/or training; or equivalent combination of education and experience is required. Previous/current experience in the medical device industry is required. Previous Laboratory experience in an R&&D environment is preferred. Testing experience is also preferred. Experience with instrumentation is preferred. Ability to use sophisticated test and measurement equipment associated with specific discipline is preferred. Reads and understands technical documentation associated with specific discipline. Ability to use PC and associated software packages. Ability to read, write, communicate and understand English is required. Must be able to successfully complete company/department training courses in manufacturing techniques. Thorough understanding and application of federal regulatory requirements (21 CFR Part 11 Electronic Records; Electronic Signatures, 211cGMP for Finished Pharmaceuticals and 820 Medical Devices; Current Good Manufacturing Practice (cGMP). Apply Now |
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Job Title: Quality Assurance Technician
Company: Glatt Air Techniques, Inc. Location: Ramsey, NJ Description: Quality Assurance Technician Located in a strategically central site in Ramsey, New Jersey, Glatt Air Techniques (GAT) was founded in 1973 as a sales and service organization serving the United States, Canadian and Puerto Rican markets. Today, Glatt Air Techniques is housed in premises spanning over 8000 sq.m., including offices, workshops and an FDA-registered cGMP development and production facility. GAT employs a workforce of over 170 in three divisions: equipment construction and sales, the Ramsey Design Group for engineering services and the Servicing Center for Technology and Contract Manufacturing. Glatt offers development and contract manufacturing of solid dosage materials, making use of top-quality fluid bed equipment for drying, granulation, layering and coating. Coating with controlled release and taste masking. We are experts in the field of fluid bed technology for the development of reliable, stable and transferable formulations and processes. This capability forms the basis for effective manufacturing with extreme reproduction accuracy. Alongside fluid bed technology, other available capabilities include wet granulation, sieving and mixing, pressing and coating of tablets. We offer excellent benefits including, 401(k), health, dental, flex spending, etc. and a comfortable work environment. Essential Job Function: Work schedule includes both weekend days and three additional days during the week. The hours are 12:00 midnight to 9:00 a.m. Issue batch records and labels for GMP batches. Review documents for accuracy, process compliance and completion. Inspect for and promote cGMP compliance in the production suites and warehouse. Ability to maintain documents neatly and accurately. General Information: Experience in the pharmaceutical industry. Bachelor’s Degree in Science field desired. JOB RESPONSIBILITIES INCLUDE BUT NOT LIMITED TO: Prepare and distribute batch records and associated documents to customers as required. Monitor and maintain the purified water systems. Inspect and verify equipment and work area cleaning operations. Investigate and prepare reports for process deviations, failures and complaints. Review and revise SOP’s and provide training. Assist in the training of new and current employees in the manufacturing, development, and quality departments regarding cGMP and other quality related issues. Monitor and maintain records for environmental control including temperature, humidity, air handling, dust collection and water systems. Calibrate and maintain physical testing equipment. Assist in customer audits as required. Interface with Contract Manufacturing and Development Departments and their customers; coordinate routine QA/QC activities for assigned customers and projects. Coordinate QA/QC activities for assigned customers: a. Raw material sampling / testing and the associated quality control documentation. b. Batch record issuance and review. c. Label preparation as required. d. Finished product sampling / testing and the associated quality control documentation. Other activities as assigned by the Group Leader or Director. |
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Job Title: Associate Quality Assurance (16E)
Company: Diebold Location: Akron, OH Description: As a Quality Assurance Associate with Diebold, you will be collaborating with a small team of passionate contributors with the goal of a successful design and delivery of solutions that provide cutting edge services to our customers. In this position, you need to be a Team player who is adept at working with other highly qualified QA, Development & Project Management personnel and enjoy the collaboration in a small team environment. You should be a self starter and have a strong commitment to work quality and deadlines and thrive in a fast-paced environment where your contribution really matters. This position will be an integral part of both our QA & Development teams. In addition to traditional product testing planning and implementation duties, you will serve as a technical resource for assisting in improving and automating the current QA processes. In conjunction with the other Services Solutions team members, perform complex testing tasks around the analysis, planning, scheduling, and implementation of Diebold’s testing efforts. Responsibilities: Test software applications to compare to functional requirements, specifications, and documentation Evaluate functionality and usability of the product Participate in the design and creation of test plans and test cases generated from functional specs and other technical specifications. Execution of both manual and automated test cases Document test results by authoring clear, concise and reproducible defect reports. Verify defect closures. Perform all aspects of verification, including functional, structural, regression, load and system testing. Design and implement test frameworks, including API, database, GUI, web stress and scalability testing Measure system performance on multi-user platforms through automated test scenarios and provide improvement recommendations Maintain ownership of design, execution and maintenance of automated testing framework, scripts and utilities. Design, publish and update automation documentation Contribute to PD process improvements |
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Job Title: QA Technicians
Company: Sunlite Plastics Location: Germantown, WI Description: Position Description QA Technicians We are a progressive medical technology company looking for a new person to join our team. Sunlite Plastics has been providing the global medical markets with quality products and services since 1946. We are a state of the art extrusion facility and ISO certified. Continued growth enables us to offer an array of exciting opportunities with career advancement potential. We promote personal and professional development in a fast-paced and energetic work environment. Qualifications: Qualified applicants must be able to read blueprints, use basic gauging equipment, perform calibrations, write procedures and inspection instructions, have knowledge of computers, knowledge of GMP’s, MIL-STD’s and S.P.C., work under minimum supervision, and have three years of related experience. Ideal candidates will have had previous supervisory experience or possess the potential to assume this responsibility. Associate’s Degree or equivalent experience required. EOE Contact Information For immediate consideration, please e-mail, fax, or mail your resume with salary history or apply in person at: Sunlite Plastics, Inc. W194 N11340 McCormick Drive Germantown, WI 53022-303 Register to View FAX Register to View *** when applying say you found this position on WisconsinJobNetwork.com *** |
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