Quality Assurance Manager Resume Examples. Food Safety Quality Assurance Supervisor July 2015 to Current Tyson - Fort Smith, AR Senior Quality Assurance Manager Resume Examples & Samples Bachelor’s degree in Computer Science, Computer or Software Engineering, or a related field and 5+ years of experience as a manager of quality assurance teams, focused on testing embedded … , Deep understanding of software development process, Determines and manages appropriate mitigation steps and solutions to resolve potentially serious product safety or quality issues, Influences direction of cross-functional teams as the Food Safety and Quality expert in the development and commercialization of new food and beverage products, Leads evaluation and development of programs to drive improvements for new and existing suppliers, Leads the troubleshooting of complex, broad-scale quality, product safety and regulatory issues. All senior specialist, quality assurance resume samples have been written by expert recruiters. Quality Assurance Resumes: So, selecting a suitable resume template is also a duty of candidate. Six Sigma Green belt or Black belt certification is a plus, Proactive in anticipating, identifying, and taking action on potential issues and problems, Proficiency to think independently and formulate conclusions consistent with the information available. Successfully led two Web Testing project as Project Leader. If you’re feeling savvy about Quality Assurance Specialist resume writing, then check out our strong Quality Assurance Specialist cover letter sample to complete your application materials. Use this resume as a template to find a job! Experience in QA Operations, production, QC and/or other relevant operational areas, but must include minimally 5 years in QA, and 3 years of management and or project management experience, Strong understanding of regulatory requirements for commercial products, Proven track record with FDA, EMEA and other Health Authorities, Strong Technical understanding of pharmaceutical processes, Team and consensus builder, with definitive and authoritative decision making ability, Ten or more years of experience in an applicable risk management environment, At least ten years of experience in quality control, quality assurance, compliance testing or audit roles for financial services company, Internal and external audit experience in banking industry, Ability to identify and clearly communicate issues, measurement criteria, cause, exposure and recommendations, Advanced to Expert level of presentation (verbal/written), relationship building and persuasion skills, Advanced to Expert understanding of Consumer Banking operations, products/services, systems and associated risks/controls, Advanced to Expert understanding of applicable laws, regulations, financial services and regulatory trends that impact consumers, Comfortable working in a team environment with layers of required review/approval, Prior leadership of staff that perform testing/monitoring activities, Bachelor’s degree in Computer Science, Computer or Software Engineering, or a related field and 5+ years of experience as a manager of high performance quality assurance teams, focused on Wireless Connectivity, 10+ years of industry experience, including at least 3+ years of hands-on testing or test automation and 5+ years as a quality assurance manager, Experience implementing and testing networking and wireless communications protocols; performing distributed systems design and testing; experience with Bluetooth, Wi-Fi and/or ZigBee including understanding of the air interface and MAC layer interactions, Strong experience managing and creating test automation frameworks, Quality Assurance best practices pertaining to test definition, requirements tracking, and test automation, Master’s degree in Computer Science, Computer or Software Engineering, with strong industry knowledge of testing Wireless Connectivity in mobile consumer electronics devices, Strong Experience with testing wireless protocols (Wi-Fi, BT/BLE, ZigBee and/or LTE/UMTS), Manage, staff, and lead a team of Quality Analysts focused on data warehousing, business intelligence, and Java applications, Maintain and implement quality assurance standards within our different Scrum teams, Participate in QA Analyst work to keep up-to-date skillsets and firsthand views on the issues, challenges, and best practices of each team - This person will need to be comfortable with rolling their sleeves up and getting stuck in with their team, Coordinate with appropriate parties to identify and prioritize next steps throughout the incident management process, Effectively advocate and disseminate Quality Assurance best practices in the team, This person will need to be comfortable with rolling their sleeves up and getting stuck in with their team, Extensive experience in software quality assurance on Enterprise Data Warehousing and Business Intelligence projects, Experience with Data Warehousing using the following technologies, Previous experience developing custom Java applications using, Direct responsibility for the corporate quality function, including quality engineering, and the corporate quality management system and tools, Indirect responsibility for site quality organizations across the company, Ensure compliance with national and international quality standards, Define and implement quality procedures in conjunction with operating staff, Support site internal and external compliance audits and drive necessary corrective action completion, Bachelor's Degree in applied science or engineering field, Minimum 5-years prior experience in Quality, Engineering or Operations Management, Demonstrated experience working with manufacturing, engineering and supply chain, Demonstrated exceptional written and oral communication skills, Proven track record of delivering results against objectives, Willingness and ability to travel, as required (up to 25% anticipated), Direct, manage and coordinate the GMP-QA team in the development, implementation, maintenance and improvement of the GMP Quality Systems, Provide day-to-day direction, support and leadership to the GMP QA associates, ensuring that the team has adequate resources and support to meet its responsibilities, Provide performance feedback and management of direct and indirect reports, Provide leadership and direction to the QA team in the absence of the QA Director, Lead and collaborate with the management team of the logistics/distribution department and of other functional areas to review key quality metrics and establish quality improvement initiatives, QC inspection and QA review of logs, products and records, Foreign site quality & GMP compliance review (for imported products), Coordination of PV activities to designated PV parties (for imported products), Maintenance and timely submissions of various regulatory GMP license amendments and renewals (DEL, MDEL, NHP-SL and OCS-LD), Creation and review of Quality Agreements with MAHs/clients and vendors/suppliers, Facility and equipment qualification/validations, Internal audits/self-inspections on GMP facilities and processes to ensure compliance with GMP, client requirements and Innomar procedures, Management of controlled documents (Policies/SOPs/WIs/Forms) request, review and issuance work flow by actively liaising with department management and other reviewers/approvers, Ensure facility and process audits as well as vendor audits are scheduled in advance and reflected in the QA audit calendar, Coordinate and host external audits by clients and/or regulatory agencies, Coordinate audit preparation activities with all impacted business units, Facilitate appropriate, effective and timely provision of documents, responses and actions during the audit, Collate responses and corrective actions with relevant impacted business units to ensure timely resolution of observations and issuance of documented responses, Provide summary and trend analyses on outcome of external audits to senior QA and functional department management, Interact with clients, internal stakeholders, vendors and various project members to ensure that specified business needs are met; assists in the post-implementation analysis to ensure that requirements are fulfilled, Manage the CAPA process for the distribution/logistics department by ensuring that non-conformance and other reportable events as well as CAPA reports are recorded, followed-up, tracked and trended, Identify, monitor and present internal/external audit and CAPA trends to department and QA management teams, Implement continual process improvements related to GMP, warehouse, distribution and regulatory processes as required, Timely submission of billing invoices to Finance for all billable QA/QC activities, Provide quality metrics for assigned areas to the QA Director on a monthly basis and on an ad-hoc basis as requested, Provide guidance to clients and internal stakeholders on GMP matters and serve as a resource to internal stakeholders for the interpretation and application of regulations and applicable guidelines, In coordination with the QA Director, prepare QA budget and manage departmental expenses, Work with the rest of the QA management team in the development/revision and implementation of QA policies and procedures as required, May also be assigned other duties and tasks as required from time to time by the QA Director, Minimum Bachelors of Science degree in chemistry, pharmacy, pharmacology or other related healthcare or pharmaceutical field, Minimum of 15 years’ experience in a senior Quality Assurance function in the pharmaceutical GMP or biotechnology industry, Minimum of 10 years’ experience in management of multiple projects (planning, implementation, management and monitoring) including budget, resource plan, Key Performance Indicators, etc, Minimum of 5 years’ experience each in the following areas, Performing/overseeing facility, process and equipment qualification/validation, Conducting internal self-inspections and vendor audits, Submission and maintenance of Health Canada facility licenses, Product quality review and Canadian QA release of imported products, Industry certification in Quality is preferred. Senior Quality Assurance Specialist Resume Examples & Samples You have a solid theoretical background with an engineering or business degree, or equivalent preferably with quality management focus You possess solid experience in quality management systems and as lead auditor, exhibiting good auditing skills in a matrix organisation Senior Quality Assurance Eng. Customized samples based on the most contacted Quality Assurance Engineer resumes from over 100 million resumes on file. Serve as Clinical QA representative on development CMC teams. Now that you’re a pro at writing Quality Assurance Specialist resumes, use our Quality Assurance Specialist cover letter sample to make an equally excellent cover letter for your job search. These responsibilities include but are not limited to, A minimum of a B.S. Quality-oriented, motivated QA Manager with 5+ years of experience establishing high-quality standards and procedures, ensuring client requirements are accurately executed and monitoring different processes. Resume Cover Letter Resume Writing FAQ. Cloud experience is desirable, Proficient in MS SQL database and MS SQL Scripting, Ability to manage multiple projects at one time, often with changing requirements as needed, Must be detail oriented, reliable and have the ability to work both in a team environment and alone with minimal direction and supervision, Good interpersonal, written and oral communication skills, Minimum of 5-7 years of progressive experience in a GMP environment required, Minimum of 5 years of Quality Assurance experience in support of GMP production required, Previous exposure to investigations and product complaints required, Must be able to interpret applicable standards and objectively make decisions, Demonstrated ability to stay abreast of trends and new information in the profession, Investigate customer complaints and non-conformance issues through to resolution, Track/Manage status /record keeping for complaints, non-conformances, and corrective and preventive actions, Assess adequacy of quality system documents (including, but not limited to policies, processes, procedures, work instructions, reference material, and forms), Design (new) and draft revisions of quality documents, Evaluate adequacy, interpret, and implement quality assurance standards, Plan, initiate, conduct, and document internal audits, Track and analyze data related to quality system metrics, Prepare reports to communicate outcomes of quality-related activities, Support maintenance of the document and records management processes, Support efforts to maintain and continually improve ongoing compliance with overall quality and industry regulatory requirements, Certifications including Quality Auditor, Quality Engineer, Quality Improvement Associate, Six Sigma, a plus, Strong computer skills including Microsoft Office applications, Knowledge of ISO 9001 and/or ISO 14001, a plus, Experience with implementation of corrective action programs, a plus, Experience with electronic document management system, a plus, Experience with work-flow based quality management system software, a plus, You have a solid theoretical background with an engineering or business degree, or equivalent preferably with quality management focus, You possess solid experience in quality management systems and as lead auditor, exhibiting good auditing skills in a matrix organisation, You have worked with quality concepts such as root cause analysis, cost of quality, QC tools and continuous improvement tools and methodologies, You possess good skills in analysing data, and you have a flair for IT, especially Excel and SharePoint, You speak, read and write Danish and English fluently, High School Degree or equivalent experience is required, Seven years of related experience is required. ), Ability to work independently and efficiently is required, Experience with Computer Assisted Audit Tools and Techniques (CAATT’S) a plus, Apply Quality Review standards and follow directions on properly applying ‘yes/no/na’ questions to determine accuracy, Provide feedback to QA team on attribute enhancements and clarifications, Participate and/or lead in calibration and rebuttal meetings, Conduct training of employees both individually or in group settings, Clearly and effectively communicate quality assurance findings to employees and managers, Captures and inputs information for error analysis and assessment, Participate when called upon for Corporate Audits, Market Conduct Exams, Maintain a solid understanding of current productions processes and quality methodology, A minimum of 6 years working experience in a Pharmaceutical Quality environment is required, A minimum 4 years working in a Pharmaceutical analytical environment (e.g., QC, Analytical R&D, or Stability laboratory) is required, A minimum of 2 years’ experience in a Pharmaceutical Stability and/or Quality Control operations position is required, Global Regulatory, Compendial and technical knowledge related to analytical & stability laboratory operations, including Part 11, is required, The ability to develop and utilize metrics for performance tracking is required, A general Understanding of laboratory systems/equipment (e.g., IQ/OQ/PQ/CSV) is required, An understanding of analytical methods (e.g., in QC environment and of validation & transfer requirements) is required, An understanding of basic statistical principles is required, Proficiency with Quality Lab Systems for events/CAPA management, change control, document management (e.g., Trackwise, ComplianceWire) is required, Ability to write and/or effectively review/critique technical documents such as lab investigations with analytical and regulatory content as it relates to laboratory operations is required, Prior experience with internal/external audits is highly preferred, This position will be located in Raritan, NJ or Titusville, NJ and may require up to 10% travel depending on business needs. Senior software Quality Assurance Apr 2015 － Present Nvidia － santa Clara, CA Serve as a key member of software development team as QA tester for Chrome,Linux for Tegra and Android Devices. Make recommendations and drive implementation based upon findings, Work directly with other key Company departments to ensure compliance and productive working relationships, You’ll work hand in hand with our development team while being part of a Quality Assurance community, Provide assistance/support with Sponsor visits, Participate in the design, development and programming of the quality assurance reports based on access to the appeal case management system, Develop and implement procedures and test plans for assuring quality in a system development environment which supports large databases and applications, Utilize MAXIMUS ISO-related documentation standards and tools to assist project team members to actively engage in and develop draft quality documents, Review Instrument qualifications to ensure that work is performed as per the procedure, Excellent working knowledge of Quality Systems and cGMP standards applicable to product life cycle from development to commercial, Strong organizational ability and problem solving capability, Strong interpersonal, communication and negotiation skills, including the ability to deal professionally with difficult individuals and problematic situations. 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