Quality Assurance Engineer Jobs in New Hampshire

Job Title: Senior Quality Engineer Company: Accellent Inc. Location: Laconia, NH Description:   The Sr. Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering. Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment.   Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.   This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.   This position is located in Laconia, NH.     Responsibilities:   ·         Maintain company compliance with FDA Quality System Regulations and ISO 13485 standards. Experience with FDA and ISO inspections and registration is a plus. ·         Actively participates in internal audits, management review and other activities covered under Accellent Quality Manual, Policies and Procedures. ·         Provide customer related quality and regulatory inquiries support. ·         Compiles and writes training material and conducts training sessions on quality control activities. ·         Provide QE direction, analysis and recommendations for Product Development to successfully launch new products into active production in a timely and cost effective manner. Directs development and maintenance of internal/external standards relative to Design and Development, ·         Lead implementation of continuous improvement projects or act as subject matter expert for SPC, FMEA, DOE and process validation. ·         Lead and provide Project Management support as needed. ·         Develops and initiates standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields. ·         Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data. ·         Performs measurement system analyses to evaluate test and inspection equipment. ·         Leads disposition of discrepant material and devises process to assess product quality and reliability. ·         Monitors and directs engineering group on calibration requirements and implementation of systems to support equipment calibration. ·         Lead supplier approval and qualification of new/revised items which includes inspection method development and validation as well as correlation with supplier’s methods, supplier audits, management of supplier corrective and preventative actions and assist in FMEA.  ·         Direct support for FDA and ISO inspections and registration. ·         Directs workers engaged in measuring, testing, and tabulating data concerning quality and reliability. ·         All other duties as assigned. ·         Up to 10% travel may be required.      Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us at www.accellent.com      Requirements:   ·         3-8 years experience in the Medical Device manufacturing industry (prefer disposable medical device manufacturing) ·         BS Engineering desired ·         Experience with FDA and ISO 13485 Certification inspections is a plus. ·         3 plus years Project Management experience, supervising diverse teams.  ·         Must be adept in use of computer software for the analysis of data, preferably Microsoft Excel and statistical packages (Minitab preferred).  ·         Quality Engineering certification (CQE) preferred or equivalent body of knowledge in areas which include, but are not limited to Statistics, SPC, Geometric Dimensioning/Tolerancing; Sampling, Design of Experiments, etc. Ability to analyze, understand and effectively communicate this technical material. Experience with Lean Manufacturing and Six Sigma is a plus. ·         Ability to organize and judge priorities in a dynamic, fast-paced environment and work independently with minimal supervision. ·         Must possess excellent verbal & written communication skills, which include but are not limited to presentation, organizational and management skills.   Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us at www.accellent.com

Job Title: SR. QUALITY ENGINEER Company: Adecco Location: Jaffrey, NH Description: Adecco Engineering and Technical, a division of the world leader in the recruitment of engineering and information technology professionals, has an immediate opening for a Sr. Quality Engineer for a direct hire opportunity with a company in Southern NH.This position will provide technical support and take a leadership role in quality engineering functions in manufacturing and product development in compliance with FDA 21CFR Part 820, ISO 13485, and internal procedures. Principal responsibilitiesDirect quality activities in manufacturing such as inspection methods and Material Review Board (MRB). Support product development such as design change and review, quality planning, risk evaluation, and validation. Supervise Quality Assurance Inspectors if needed. Coordinate Corrective and Preventive Action (CAPA) for customer, internal, and vendor related needs. Audit internal and vendor processes and procedures. Participate in Continuous Improvement Projects (CIP) for both processes and business systems. Develop training programs for inspection and engineering. Represent company during customer or regulatory audits as needed. Job Specifications EducationMust have a B.S. (technical degree preferred) Work experienceMinimum 7-8 years QA engineering experience in a medical device manufacturing environmentASQ certification Medical Devices Experience RequiredExtrusion Experience Preferred Knowledge/SkillsRegulatory cGMP, QSR and ISO knowledge base Computer literate (MS Word, Excel, Access, PowerPoint, and Mini-tab preferred) Negotiation and problem solving skills Good oral and written communication skills Statistical Skills (DOE, SPC, Reliability, Gage R&R) Experience with risk analysis methodologies Experience in the area of manufacturing operationsAbility to prioritize and work independently Validation concepts & techniques (process, equipment, and gauging) Experience developing training programs Able to work independently with limited supervision Working Conditions and Physical Demands Exposure to high production/output machinery and equipment, and constant noise in the production/plant environment. Engages in walking, sitting, lifting, bending, carrying, talking, and hearing. Ability to travel to customers and vendors (under 10%). The job description documents the general nature and level of work but is not intended to be a comprehensive list of all activities, duties, and responsibilities required of job incumbents. Consequently, job incumbents may be asked to perform other duties as required.

Job Title: Quality Engineer IPC-610 Company: Location: Andover, NH Description: This is for a growing electronic contract manufacturing company with locations worldwide. You will act as liaison between company and customesr with respect to technical or quality issues. Provide engineering support to resolve quality issues, and help to correct or improve manufacturing processes. Provide constant support to the Quality Management System to ensure compliance with current ISO standards. Responsible for managing and documenting the following ISO Sections: Internal Audit System (also performs Internal and external audits), calibration of measuring and testing equipment, corrective and preventive action system, control of non-conforming assemblies & MRB dispositions. Analysis of manufacturing and test yields to conduct quality meetings, maintenance of quality records, member of the Continual Improvement Committee, and participate in customer audits as a secondary management representative. Provide IPC A 610 workers proficiency training at all levels which may include IPC certification. Qualifications: Ability to maintain multiple projects and respond quickly and decisively to production support requests. A strong working knowledge of ISO 9001:2000, SPC, problem solving, process auditing and Microsoft Office. IPC Workmanship Standards knowledge (IPC 600, 610, & J-STD-001). Failure analysis and MRB experience, with the ability to interact with customers. * Prior experience working with a conract manufacturing facility a plus.

Job Title: Quality Assurance Engineer Company: TEKsystems Location: Portsmouth, NH Description: Position Summary:Assist in computer-based testing and analysis of future products for theOffice of Technology Division. Write and execute test cases ensuringprojects and products are delivered conforming to software quality assurancestandards and project specifications.Description of Duties:- Write and execute Quality Assurance test cases associated with applicationsoftware and systems.- Identifies, analyze, and documents defects, questionable functions,errors, and inconsistencies in software program functions. Verify fixeddefects as corrected.- Install, maintains and use testing software programs.- Create test cases and data, and execute automated test scripts usingtesting software programs.- Set up and organize lab configurations for functional and system testing.- Document, track, and communicate test plans, test results, analyses, andunresolved problems.- Develop computer programs to test, track, and verify defects in softwareprograms.- Use Microsoft Office suite of products proficiently including Word, Excel,Outlook, Project and PowerPoint and issue tracking systems.Qualifications:- BS in Computer Science or related discipline required- Minimum of three years of software QA experience, including experience indesigning software/application in .Visual C#.Net, and testing Webapplications in Windows and Macintosh enterprise environment.- Experience in setting up and utilizing complex lab configurations,servers, firewalls, routers, hubs, and RDBMS databases such as Microsoft SQLServer and/or Oracle.Join TEKsystems() and get your career on the fast track. As the leadingtechnology staffing and services firm, we are passionate about deployinghigh-caliber IT and communications expertise. To satisfy our constant needfor expertise, we actively seek talented Technical Professionals with alllevels of information technology and communications skills. TEKsystems knowsthat every professional has different needs, so we'll work together todetermine a suitable benefits package. We offer options to our TechnicalProfessionals that could include: a health plan, 401k, provisions forvacation and holiday pay, and technical and professional training. With afoundation as the nation's largest IT staffing firm, we've become abillion-dollar services company by blending superior client service with anunrivaled ability to source and manage talent to precise specifications,resulting in successful technology executions. Allegis Group and itssubsidiaries are equal opportunity employers. M/F/D/V

Job Title: Quality Engineer (290858-723) Company: Not Specified Location: Rochester, NH Description: 290858-723 Job Description Develop, implement, and maintain quality standards for manufacturing processes. Devise and implement methods and procedures for inspecting, testing, and evaluating production components and assemblies. Design and/or specify inspection and test methods and equipment. Develop and implement quality assurance test and perform statistical analysis for development & production programs. Lead Failure Mode Effect Analysis (FMEA) activities enabling improvements in process control and capability. Initiate and sustain MRB (Material Review Board) process in support of appropriate product disposition. Required Skills Definition of fundamental product/process design and control plans Measurement and test methods supporting GD&T, metrology techniques Statistical analysis (JMP, Minitab) skills with strong attention to detail MSOffice proficient (Excel, Powerpoint and Visio skills required) ASQ Certified Quality Engineer (CQE) given preference. Required Experience BS Engineering degree, ME/IE/MfgE preferred. 3-5 years experience in quality/manufacturing industry using MRP/ERP (SAP, Oracle, etc.) Experience in ISO 9001/AS9100 Quality Assurance Systems Proven problem solving skills in a teamwork setting. Demonstrated interpersonal and communication skills, oral and written. Ability to read and understand blueprints/drawings, CAD experiences a plus. Lean, Six Sigma, or Process Excellence certification experience preferred  Job Location Rochester, NH, US. Position Type Full-Time/Regular

Job Title: Quality Assurance Engineer Company: Janco Electronics, Inc. Location: Dover, NH Description: Responsible for assuring compliance with all applicable quality standards in the company.  This includes the developmentof systems and documentation required to monitor and assure compliance such as vendor approval ratings, corrective action reporting, material review requests and compliant reports.  Generate and implement QC standards, establish manufacturing procedures for new customers and products, maintain quality files, interpret and implement ECO's, and oversee the training of employees regarding the maintenance of quality standards.  Monitor quality standards via audits conducted by QA team to assure the integrity of the company's systems and procedures.  Maintain and enhance the ISO 9001 abd ISO 14385 programs.

Job Title: QA Engineer with .NET skills Company: Alexander Technology Group Location: Manchester, NH Description: Alexander Technology Group is seeking a QA Engineer for a contract to hire opportunity.  The client is in the Bedford NH area.  This position will work closely with the software development team to validate new features and functions, verify the production readiness as well as develop and implement automated testing tools The products are built on the .Net platform and are developed in an Agile environment.  The ideal candidate will have a mix of QA and .net coding abilities Duties- Manual and automated testing; developing test plans as well as creating and executing of test scripts - Execute system, integration, regression, stress, scalability, and performance tests; track and report metrics of product quality - Manage QA lab resources   Required Skills:- Ability to design and performing tests at the code or component level in a .NET environment - Strong verbal and written communications skills - Self-directed and process-oriented - Experience with SQL - QA tools and automation is a plus   Education:- Bachelor's Degree and at least two years experience in a .NET environment working as a white box tester or a mix of development and test experience - Migration and/or integration experience is a plus - Agile development is a plus   Please send your resume to Jon Moller at Register to View

Job Title: QA Engineer Company: Location: Manchester, NH Description: This is a full-time, permanent position with one of my top clients. This role is open to U.S. Citizens and Green Card holders only, local candidates please. Thank you very much and I look forward to hearing from you! Responsibilities: Develop and maintain test plans Create and execute test scripts Work closely with software engineers to develop and implement manual and automated tests Execute system, integration, regression, stress, scalability, and performance tests Track and report metrics of product quality Manage QA lab resources Work with software engineers to enhance the testability of the product Review product documentation Work with Support as needed to resolve customer issues Required Skills: Knowledge of CRM or ERP applications, particularly in the areas of sales force automation and order management Strong verbal and written communications skills Self-directed and process-oriented Experience with SQL and Windows operating systems QA tools and automation experience

Job Title: Quality Engineer (MJ) Company: Atrium Medical Corporation Location: Hudson, NH Description: About the Company"Hundreds of Atrium employees around the world enjoy a great sense of pride stemming from our commitment to quality, customer service and our passion for innovation.  Recognizing that everything we do somehow touches the lives of millions of patients each year is further evidence of our commitment to quality."Steve HerweckFounder, Chairman and CEO Founded in 1981, Atrium is a diversified healthcare provider where improved patient outcomes is "job one" for every member of the firm.  Workmanship in the quality products we build is reflected in Atrium's worldwide demand for over 2.7 million sterile medical products manufactured and distributed to over 60 countries each year.  Our commitment to ISO 13485 Quality Standards and pioneering discoveries in research, product development and manufacturing has enabled the company to excel in market leadership in nearly every healthcare segment we serve.Atrium is a world class organization dedicated to innovation, research and development, state-of-the-art manufacturing, customer service, clinical education, professional marketing and sales, and global logistics.  Atrium is a progressive business enterprise that experiences strong employee loyalty and long-term commitment and contributions.  However, Atrium's ambitious growth strategies in an evolving healthcare industry requires a constant pool of talented resources at all levels of the company.From cardiac cath-lab to operating room, Atrium continues to invest in those leading edge technologies that best satisfy our financial goals and contribute to important advancements in patient care.  Combining advanced automation with global manufacturing resources, together with extraordinary advances in biomaterials science, our diversified portfolio of critical care products are leading the way to brighter, more clinically effective solutions in cardiovascular disease, soft tissue repair and critical care management. Overview: Support Atrium product development teams throughout the development process.  Conduct and review activities in the areas of validation, quality control, risk management and product development to ensure continued compliance to standards and regulations and sound statical methodologies.  Support manufacturing by investigating process deviations and assisting in equipment qualification and process validation.Use Your Skills and Expertise To: Provide complete and accurate quality plans for each assigned project.  This includes planning for product development, design and process changes, and additions to existing product lines.  Maintain quality plans at all stages throughout product life. Work with suppliers and contract agencies to provide documentation demonstrating that products and services meet the requirements of the Quality Management System and applicable standards.Analyze non-conforming conditions and material as necessary to implement corrective actions.Perform and analyze process capability studies, designed experiments and special studies necessary to support departmental efforts.Participate in cross functional design and development teams.Performs other related duties as required.Qualifications  Bachelor's Degree in Engineering or Science.  A minimum of three years related manufacturing experience in a QSR, medical device environment.  Knowledge of Quality Assurance methods, such as process validation, design of experiments, statistical process control (SPC) and protocol/report preparation is mandatory.  Knowledge of ISO 13485 and FDA requirements.  Good analytical and problem solving skills.  Effective verbal and written communication and interpersonal skills.  High level of attention to detail and accuracy required.We Offer:Atrium Medical Corporation offers Competitive Salaries, Exceptional Benefits (Health/Dental/Summer Work Hours Program/Disability Insurance/EAP Program/ Opt Out Program/and a Business Casual Dress Code and MUCH MORE!!!We do not accept unsolicited Agency Resumes. Atrium Medical Corporation is an equal opportunity employer dedicated to workforce diversity and a drug and smoke-free environment. Drug screening is required. NO PHONE CALLS PLEASE.

Job Title: White Box QA Engineer Company: Location: Manchester, NH Description: This is a full-time, permanent position with one of my top clients. This role is open to U.S. Citizens and Green Card holders only, local candidates please. Thank you very much and I look forward to hearing from you! Responsibilities: Develop and maintain test plans Create and execute test scripts Develop test harnesses in C# to test low level components Work closely with software engineers to develop and implement automated testing tools Execute system, integration, regression, stress, scalability, and performance tests Track and report metrics of product quality Manage QA lab resources Work with software engineers to enhance the testability of the product Required Skills: Ability to design and performing tests at the code or component level in a .NET environment Strong verbal and written communications skills Self-directed and process-oriented Experience with SQL QA tools and automation is a plus Education: Bachelor?s Degree At least two years experience in a .NET environment working as a white box tester or a mix of development and test experience Migration and/or integration experience is a plus Agile development is a plus