QA Manager Jobs in Massachusetts

Job Title: Quality Engineer/Manager Company: Euro Pro Location: Newton, MA Description: Euro-Pro, a pioneer in innovative cleaning solutions and small household appliances, seeks a top talent Quality Program Manager/Engineer to join the team in Newton, MA. Founded over a century ago and recognized as a global leader and innovator in the industry, we continue to exceed expectations by providing today’s busy consumer with better and more efficient products that fit their lifestyle and make life easier. From cutting-edge chemical-free steam mops to state of the art kitchen appliances, Euro-Pro products are made and sold under the brand names of Euro-Pro, Shark, Ninja Infinity, and Bravetti. This position will be responsible for Quality and Reliability Engineering for a product category. Duties include: * Work with Engineering and Marketing to identify customer expectations for new products or product improvements * Work with Engineering to establish solid and testable specifications to ensure products meet market requirements * Work with Engineering during the design phase to ensure that products meet requirements * Conduct and coordinate testing activities in multiple locations * Work with engineering and manufacturing to drive continuous improvements of products To be qualified for this position you must have: * Bachelors’ in Engineering or equivalent field * 10 years experience in technical or project management role * 5 years experience in consumer appliances * 5 years experience in quality and/or reliability engineering * Experience conducting FMEA and detailed design review * Experience in design engineering and/or manufacturing preferred * Experience with Six Sigma or other quality programs preferred At Euro-Pro, we are driven to be the best in the industry. We are looking for individuals who want to make a difference. We celebrate and reward initiative, creativity, growth, and commitment to our mission. We will provide the challenge and the opportunity to apply all aspects of your experience and skills; you provide the energy, passion, and results. If you would like to explore a possible fit with our dynamic and growing company, please forward your cover letter, resume, and salary history to Register to View -pro.com. No phone calls please. Euro Pro is an EEO/AA employer Search words: consumer goods, consumer products, housewares, appliances, kitchenware, vacuum, hand vac, sweeper, toaster over, slow cooker, blender

Job Title: RN Directors, QA,Infectious Control,Case Managers, Nursing Education, PA/NP,Homecare, Hospice Company: Enid, Chesterfield & Company, Location: Boston, MA Description: RN Directors, QA,Infectious Control,Case Managers, Nursing Education, PA/NP,Homecare, Hospice: email: Register to View PA,NP,Physicians,Directors Case Managers, Staff Devel, Nursing Admin, Nurse Education,Homecare, Hospice/All RNs. Nursing Admin roles!!LTC, CASE MANAGERS, MASSACHUSETTS Register to View With Enid, Chesterfield & Company (link) you work with a seasoned group of professional recruiters dedicated to staffing excellence. With vast networks of exclusive contacts, our experts work locally within one industry to ensure you the best service. Contact us to see the doors we can open for you.

Job Title: Clinical Manager (RN Manager) - Quality Assurance Company: Caretenders Location: Newton, MA Description: Unique Leadership Opportunity With A Leader in Home Healthcare: Recognized For Excellence By Forbes and FortuneIt's all about helping people achieve more!    Caretenders is a proud member of Almost Family, a leading provider of home health nursing, rehabilitation and personal care services.  Our Senior Advocacy Mission raises the bar with programs designed to achieve better outcomes for our patients.  For over 30 years, we have developed a culture that fosters innovation, clinical excellence, and integrity.    Why consider choosing a career with us?  Because we are committed to helping you achieve your goals.  As a member of our Senior Advocacy Care Team, we are confident you will achieve more for your career with industry-leading specialty programs that enhance care and promote better outcomes for patients.  You will enjoy the support of a progressive group along with great benefits, competitive pay, and flexible schedule options to fit your lifestyle.

Job Title: Manager of Quality Assurance - (Mgr Systems/Software E Company: HP Location: Boston, MA Description: HP is a leading global provider of products, technologies, solutions and services to consumers and business. The company's offerings span IT infrastructure, personal computing and access devices, global services, and imaging and printing. Our $4 billion annual R&D investment fuels the invention of products, solutions and new technologies so we can better serve customers and enter new markets. We invent, engineer and deliver technology solutions that drive business value, create social value and improve the lives of our customers.This position is for a Manager at either HP's Andover, MA or Fort Collins, CO locations. They will be working in the new Unified Storage Division (USD), part of Hewlett Packard's Storage Works Division (SWD) as the manager of NAS QA.   As the Manager of Quality Assurance the candidate must be able to set overall expectations pertaining to setting accurate schedules, costs and resources in support of new product launch. Ensure delivery against QA department goals and objectives. Provide necessary definition, development and deployment of product quality assurance strategy. Directly supervise quality assurance team leads, quality assurance engineers and testers including the preparation and delivery of staff performance evaluations and career development activities. Provide technical guidance as required.   Responsibilities:   Work with development to determine QA requirements and test coverage and coverage with input from marketing and customer support.Manage other QA teams in US, and India to ensure comprehensive test coverage and quality assurance of productsDeliver high quality releasesProvide high level technical directions and leadership to the teamInput to planning timelines for both engineering and quality assurance.Standardize practices and procedures based on a software development methodologyDrive implementation and usage of test automationEffectively work across multiple functions and geographies.Manage, coach and motivate team member to ensure a highly productive and efficient teamResponsible for staffing, budget setting and resource managementEstablish and maintain policy for documentation of all products.Provides effective communication regarding issues, objectives, initiatives and performance to plan. Job specification of Quality Assurance Manager   BS/BA degree in computer science, engineering or related discipline.Minimum of 8 years of quality assurance experience, and 3 years at management position.Strong understanding of different software development life cycles and contemporary software quality assurance processes and automated tools.Must have experience in managing and working with distributed team members.Strong analytical skills and experience with implementation and administration of Quality Assurance metrics, such as defect profiles and performance to entry/exit criteriaExcellent problem solving, interpersonal communication and project management skills a must.Strong leadership skills that inspire team confidence and respect while motivating team members in a creative and effective manner.Must have a desire for achieving excellence in customer satisfaction, process and product quality and reliability.

Job Title: Director of Quality Assurance and Regulatory Affairs Company: Company Confidential Location: North Andover, MA Description: POSITION OVERVIEW The Director of Quality Assurance and Regulatory Affairs is responsible for the overall development, implementation and coordination of Quality Management Systems and Regulatory strategies and activities in accordance with the Medical Device Company's policies and procedures and FDA's Quality System Requirements (QSR) and European Medical Device Directive (93/42/EEC) and ISO 13485. JOB / DUTIES / RESPONSIBILITIES ? Ensures that the Company is compliant, effective and efficient and will easily withstand audits by regulatory agencies and third parties; ? Is responsible to develop, coordinate prepare, compile, submit, and maintain domestic FDA 510(k) submissions and international EU Technical Files; ? Effectively functions as the company representative and the Senior Quality and Regulatory contact and strategist with the FDA, international regulatory agencies and Notified Bodies; ? Serves as the FDA correspondent and FDA audit liaison as well as the company’s Management Representative for ISO 13485;? Monitors the US and international regulatory environments, and provides executive management with assessments of the impact of new and changing regulations on the company's business in respect to compliance to most current regulatory requirements (FDA, MDD, CMDCAS);? Translates Quality and Regulatory Requirements into terms understood by the business and process owners resulting in efficient solutions to worldwide regulatory compliance. Assists in the preparations of policies and procedures to comply with regulatory requirements; ? Coordinates the review and approval of product labeling and advertising. Review marketing promotional materials and provides leadership /guidance in the development of compliant sales training, advertising and detail literature;? Maintains Company's customer complaint systems including complaint investigations and trending;? Establishes and oversees the Company's internal auditing and external supplier management audit programs and reports findings to executive management;? Develops, implements and maintains QSR and ISO 13485 compliant design change processes;? Provides input to proposals and project plans to ensure the product development process meets FDA clearances approvals including appropriate Verification and Validation activities.?Provides compliant Quality and Regulatory strategies to support, encourage, and deliver innovative ideas from proof of concept through end of product life;? Has familiarity with Normative Standards applied to medical devices, specifically magnetic resonance imaging systems; ? Develops and implements QSR/GMP training programs for direct reports and other functional groups to assure awareness of all requirements and maintain compliance with all current regulations; ? Provides direction and effective leadership and development activities to the Quality and Regulatory team; ? Utilizes influence and respect to gain the support of the cross functional business function leaders; and? Coordinates safety agency testing and approval; JOB QUALIFICATIONS Requirements ? Bachelor's Degree in Business, Sciences (Chemistry, Biological Sciences, Physics or related field) or Engineering or related field. Master's preferred. ? Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA) or Certified Quality Manager (CQM) and/ or Regulatory Affairs Professional (RAC) certification a plus. ? Knowledge and demonstrated effective use of FDA QSR, European MDD and ISO 13485 quality system requirements. ? Working knowledge of medical device development process and European, US and international regulations, laws and standards covering medical devices. ? 10+ years of progressively responsible Quality Systems and Regulatory management experience in the medical device industry with a proven track record of successful assessments by FDA and Notified Bodies. ? A progressive record of increasing responsibility in quality assurance and regulatory affairs. ? Experience with medical device regulatory submissions for FDA 510(k) submissions and European technical files with proven experience negotiating with regulatory agencies. ? Strong working knowledge of U. S. FDA and EU regulations and standards. ? Strong leadership, influencing, negotiation and people management skills ? Strong project management skills, organizational, and problem solving skills ? Excellent writing and communication skills. ? Ability to work independently and to take a leadership role in the QA/RA processes. ? Ability to lead discussions with executive management team on strategy and policy issues. ? Ability to understand, interpret and explain complex device development details and regulations to non-experts ? Must maintain and communicate high ethical standards and respect.

Job Title: Quality Assurance Manager Company: Veritude Location: Boston, MA Description: We are looking for a Quality Assurance Engineer on behalf of our client, Fidelity Investments.This position is based in Boston, MA.SummaryAsset Allocation Technology (AAT), a division of Fidelity Investment Management Technology (FIMT), develops and supports research, portfolio construction and investment operation applications for the Asset Allocation Division (AAD). AAD comprises of five lines of business including account management (focuses upon minimizing tax liabilities), model management (portfolio growth), funds management (college savings, retirement savings), financial solutions (investment methodology for the tools on fidelity.com) and intermediary solutions (new business opportunities for AAD).As part of the FIMT horizontal Quality Assurance organization, AAT is seeking a Principal Quality Assurance Engineer to lead AATs strategic Data Architecture program within the Infrastructure product line. The Data Architecture program is aimed at re-architecting the entire data environment within AAD and eliminating three legacy database platforms. This work plan is designed to coincide with key business initiatives and large portion of the build phase is to be performed off-shore. Due to the scope of work, the critical dependencies to key business objectives and need to have tight coordination with off-shore partners, the existing AAT Quality Assurance team requires an additional lead to manage, plan and drive this workload.ResponsibilitiesThe primary responsibilities of the Data Architecture QA Lead role focus on developing the overall test strategy including use of testing tools and the management of its entire execution. This includes defining test strategies, developing test plans, overseeing creation of test cases, test execution, and results reporting. This role will also entail the workload allocation of a small team of onshore and much larger team of offshore professional services functional testers. Additional responsibilities include:Provide tight testing coordination between interim key business initiatives and the overall Data Architecture test strategy with the project teamAble to be highly productive in an agile project delivery environmentReview requirements/design documentation and implement comprehensive test plans covering this materialLead defect review meetings with business analysts, developers and fellow QA team membersDetect scope changes and escalate issues as appropriateProactively communicating with developers and business analysts to resolve issues or questions pertaining to test creation or executionDemonstrating strong interpersonal, relationship building/relationship management and facilitation skillsLogging of defects when required and Implementation of traceability between test cases and requirements documentationWorking closely with QA Automation Engineers to identify test cases conducive to automationAccurate and timely status reporting with Manager, including issues prohibiting progress when appropriate

Job Title: Sr. Manager, Quality Assurance Company: VistaPrint Location: Lexington, MA Description: About Vistaprint: Through a revolutionary business model supported by patented and proprietary technologies, Vistaprint does what no one else can. We deliver high-quality printed products in low volumes for a great price. It is our goal to astound customers by giving them the easiest way to make an impression for less. Our customers are both small businesses and consumers * essentially anyone who needs high-quality, low-volume printing or easy-to-use electronic services, at a great value. Over the years, our customers have come to trust us because of our low prices, convenient online ordering and high-quality products. Our products range from business cards, brochures and postcards to invitations, note pads and thank you notes. Vistaprint also provides online services and solutions, such as Email Marketing, Websites and Postcard Marketing. Job description:As Senior Manager of Quality Assurance, you will manage our Channel program, which consists of three teams supporting the customer interaction sides of the Vistaprint website, our internal customer service tools and our partner sites. In this position you will work closely with the Director of Quality Assurance to define and drive the QA roadmap and lead the evolution of methodologies to achieve higher levels of quality.Responsibilities:* Collaborate with senior business leaders to support the Marketing roadmap* Coach and train team members in the use of continuous improvement tools and best practices* Drive quality throughout the software development lifecycle* Implement and define metrics for tracking our test-automation strategy using internal test harnesses and 3rd party automation technologiesSkills and Qualifications:* 5+ years experience managing QA/Automation Engineers of web-based applications, preferably in a high-volume retail environment* Previous experience involving QA Best Practice implementations * Strong technical skills including knowledge of Microsoft .NET Technologies* Strong database knowledge* Strong experience building software, testing dashboards and establishing metrics for progress tracking* Self-motivated and team-oriented* Strong analytical, troubleshooting and organizational skills* Strong communication skills* Commitment to deadlines and willingness to meet the needs of a 24x7 organization* Ability to plan, organize and execute software test projects* Bachelor of Science in Computer Science, Engineering or applicable disciplineEqual Employment Opportunity Employer: Vistaprint is an Equal Employment Opportunity Employer. All qualified candidates will receive consideration for employment without regard to race, national origin, gender, age, religion, sexual orientation, veteran status or marital status. Agencies: Vistaprint does not accept unsolicited candidate referrals or resumes from third party vendors, including recruitment agencies. Only resumes received from contracted agencies/vendors will be considered. Vistaprint will not be responsible or liable for any fees or costs associated with such unsolicited submissions.

Job Title: Manager of Quality Assurance-Healthcare Client Services Company: EOS CCA Location: Norwell, MA Description: Collecto, Inc., d/b/a EOS CCA is a privately held National Debt Management and Recovery Resource Company. The corporation is headquartered in Norwell (Boston), Massachusetts and has regional centers in Chicago, Dallas, Denver and Brockton, MA. EOS CCA is a division of EOS, one of Europe's largest accounts receivable outsource companies, which provides EOS CCA with a worldwide presence. EOS employs over 3,000 professionals in the United Kingdom, Germany and other principal countries in Europe. EOS CCA is the United States Recovery Management Division of EOS, creating a truly international accounts receivable outsourcing company (ARO) with unmatched global resources and experience. EOS CCA is seeking a Manager of Quality Assurance in  Healthcare Client Services to monitor and provide quality control for all processes relating to our healthcare clients . This position will be located in Norwell and Brockton and will require 2 plus years previous Healthcare collections, auditing, compliance and systems experience. To ensure all client deliverables are met on time, this position is responsible to coordinate internal processes and communicate with all  Sales and Operations and IT departments. Strong organizational and time management skills required.   Responsibilities also include monitoring tracking sheets, verifying data and follow-up on all  internal processes to ensure issues/client invoices are being resolved. Must be analytical and be able to problem solve. Previous experience in a healthcare collections quality assurance department preferred.    The ideal candidate will have strong verbal and written skills, knowledge of FACS, tactics and report writer. Solid understanding of Microsoft Office Suite a must. Bachelor's degree a plus. EOS-CCA offers a competitive salary, full benefits package and a 401K with company match and more. To be considered for this position, please submit a cover letter and resume including salary requirements to  www.eos-cca.com or Register to View -cca.com . LOCAL CANDIDATES PLEASE.   Job Requirements:Req. Code : 51 Division/Department : Norwell Shift/Hours : First Shift (Day) % of Travel Required : 20-30%

Job Title: QA Manager Company: Hollister Location: Boston, MA Description: Role: QA ManagerRequired Skills* Expert in development life cycle and best practices* Ability to successfully track multiple projects* Ability to created detailed documentation* Proven track record mentoring test engineers* SDK and API level testing* Mobile testing (iPhone, Symbian, Windows Mobile,Android)HUGE PLUS* Strong knowledge of web application testing* Solid understanding of performance testing* Experience with automation (mobile is a plus)experienced, hands-on QA Manager. Responsibilities:The candidate must have experience in a fast paced, start-up environment.This role will be hands-on; directly involved in day to day testing.The manager will lead the testing team's efforts across several concurrent projects.You will be working in a Client/Server - Linux, Windows, and Mac OSX enviroment. Testing Mobile - iPhone, Symbian, Windows Mobile, and Android. Working in a Java/C++/C enviroment.* r

Job Title: Director - Quality Assurance Company: Genzyme Location: Framingham, MA Description: Genzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzyme's people and culture have been consistently recognized for excellence. For example, we have been named several times to Fortune's list of the 100 Best Companies to Work For in the United States. We also consistently rank among the top employers for scientists in surveys of Science readers. Genzyme's local offices and facilities in Europe and other parts of the world have earned similar distinction as respected employers. By applying for a position with Genzyme, you are taking the first step toward becoming a part of our dynamic and talented team, and sharing in our continued success.Director, Quality Assurance - Framingham, MAThis individual will report to the Senior Director of Quality Operations for Genzyme Framingham, MA Biologic and will be responsible for providing leadership and technical management of the Quality Assurance Team. The position will have 2 direct reports with a total organization of approximately 50 people. The primary responsibilities of the groups include developing and assuring efficient and compliant Quality Systems are in place and providing appropriate Quality review to meet bulk, and finished product lot release schedules for world wide distribution of the three products. The scope of manufacturing operations at the various Framingham sites includes buffer and media preparation, cell culture and purification.Major responsibilities include:• Identifying quality improvement opportunities within operations and partnering with peers in Manufacturing and Quality Ops at the site to develop and implement solutions. Evaluate, propose and implement new processes and technologies as alternatives to optimize efficiencies in the departments.• Setting goals for manufacturing and quality improvements and ensuring that effective metrics with targets are utilized to track performance.• Ensuring that site Quality Assurance practices are consistent with corporate quality standards as appropriate and corrections are put in place to address gaps.• Developing and managing departmental budgets in cooperation with direct staff.• Supporting an environment of staff development and learning. Providing feedback to direct reports in a timely manner. Managing performance issues and soliciting the appropriate input from HR and management. Writing and administering performance appraisals on time and in a thorough and thoughtful manner.• Developing and executing hiring plans. Ensuring that requisitions are interviewed for and filled in a timely manner.• Keeping senior management apprised of product issues, dispositions and quality improvement plans.• Interacting with regulatory agencies to present production records and applicable data, explain incidents, trends and reports as needed during site inspections.• Developing a cohesive team, maintaining and reinforcing a strong quality presence in the manufacturing areas, encouraging positive relationships and networking effectively across sites and organizations.The applicant should have demonstrated experience in batch record review and accuracy, product disposition, process deviation and product technical investigation review within bulk drug substance manufacturing operations. Extensive knowledge of fundamentals in the Biotechnology/Pharmaceutical fields and hands on technical expertise is required. Comprehensive knowledge of FDA and EMEA regulations and experience in US and international regulatory agency audits and inspections of the biopharmaceutical industry, including, but not limited, to aseptic processing of biologics is essential. Excellent technical writing skills are necessary as well as a working knowledge of statistical analysis, process controls, and software and method validations. Familiarity with automated operations processing Manufacturing Execution System (MES), and other electronic quality system tools such as Trackwise, and/or Catsweb is desirable.