Watchful Quality Assurance professional with the ability to detect imperfections in technology products and devise quick tests to check for errors without slowing up the manufacturing process. Collaborative working style, ability to manage through conflict, and ability to find creative and practical solutions to problems, Detail oriented and proven ability to multi-task, Bachelor's degree is required; advanced degree or certification a plus, Familiarity with using PCs and navigating programs, Must have the ability to carry out detailed but uninvolved written or verbal instructions; deal with variables as they present themselves, Ability to do simple addition and subtraction; copying figures, counting and recording, Possess the ability to understand and follow verbal or demonstrated instructions; request supplies orally or in writing, Visual requirements include clarity of vision at a distance of more than 20 inches and less than 30 feet with color vision, depth perception and field of vision, Bachelor's degree in applicable field of study or equivalent job experience, Three years experience in a GMP environment such as blood banking, pharmaceutical, medical devices or a hospital, Two years experience in QA, QC or Quality Auditing, Knowledge of federal regulatory requirements pertinent to pharmaceutical, biologic or medical device manufacturing, Demonstrated effective verbal and written skills. They must be able to identify opportunities for process enhancements while supporting existing standards with a focus towards providing excellent service to our clients. Quality Assurance resume samples most often mention skills in testing, technical, test, quality assurance, software, processes, system, engineering, activities and compliance. * Data reflects analysis made on over 1M resume profiles and examples over the last 2 years from Enhancv.com. Identified test scenarios, estimated test effort, and created test plans. The combination of these two qualifications should already create distance between Aaron and the other applicants. Quality Assurance Specialist Resume Samples amp Templates. performance of root cause analysis), Experience with MS Office Suite (Excel, Word, PowerPoint), Demonstrated ability to manage multiple priority projects/workload, ensuring timely completion, Ability to work well independently as well as part of a team, Ability to stay organized, manage time, and work on multiple documents/projects at once, Excellent interpersonal skills with the ability to adapt effectively to rapidly changing organization issues, Experience writing and supporting pharmaceutical manufacturing deviations and investigations, Knowledge of product complaints processing, stability protocols, manufacturing activities, A minimum of a Bachelor’s degree (or equivalent) is required, A minimum of 4 years of related experience within a GMP environment is required, Strong knowledge of regulatory cGMP and CFR is required, Knowledge/understanding of drug manufacturing and packaging processes from sampling and inspection through warehouse distribution is preferred, Knowledge/understanding of Batch Record Review, Product Release, Raw material and packaging components review and approval is required, Knowledge/understanding of the product development life cycle is required, Knowledge/understanding in various computer systems: ERP, LIMS, MES and Microsoft Office (including Outlook, Word, Project, Excel, PowerPoint) is preferred, Understanding of PLC programs is preferred, Ability to work 2nd shift hours with flexibility for 1st shift when needed is required, This position will be located in Fort Washington, PA and will require up to 5% local travel as business needs require.Quality Assurance, Perform enhanced due diligence and annual refresh for GBM high risk clients, Working under guidance of AML Advisor/Director Quality Assurance to ensure proper execution and maintenance of AML controls, Assisting in the training needs for the business lines, and the development or presentation of the training as appropriate; and, Developing and reporting metrics and preparing management reports for Business Line Compliance Op Risk and executive meetings, Minimum of 5 years in financial services and/or AML/ATF compliance, Minimum Bachelor’s degree in business, related field, finance, audit or equivalent experience, Strong communications, analytical, organizational, project management, and planning skills, Knowledge of businesses, products, operations, systems, and organization; and, Concentrated use of visual attention is required when reviewing agreements. Do you have a talent for listening and the ability to communicate easily with others? Successful completion of PPD Foundation Training, Live Our Values: People, Service, Quality and Innovation, Rework product that requires improved packaging or labeling, Inspect the quality, durability, and consistency of product, Ensure product stored/putaway/picked/shipped accurately and in a manner that will not damage the items, Comply with individual, team and departmental productivity and performance goals, Conduct operations in a manner which promotes safety and in accordance with federal, state, and local laws, Perform or assist in building, grounds, and housekeeping as required, Abide by all security policies and procedures, Ensure that the warehouse is consistently clean and free of debris, 1 – 3 years of related work experience in Auditing, Detail oriented and good organization skill, Self-starter and good problem solving skills, Ability to work in a multi-task environment, Associates degree from an accredited college, Fluent in Spanish – not required, but would be a plus, Conduct quality assurance testing of line of business execution against firm-wide Third Party Oversight standards, Evaluate line of business control processes to determine their effectiveness and compliance with firm-wide standards, Conduct root cause analysis to determine source of business execution issues or ineffective controls, Partner with lines of business to determine appropriate remediation for identified issues, Validate effectiveness of remediation actions via discretionary quality assurance testing, Manage the efficient, timely entry and maintenance of documentation, Design and execute test plans on web applications, Work very close with the rest of the development team to ensure the feature satisfies stakeholder expectations, Contribute to our automated tests library, Experience driving best practices in adoption and use of the advanced quality assurance techniques, including test automation, white and black box testing, predictive models, risk analysis, requirements engineering, test driven development,security testing, and continuous integration, build and release management, Hands on experience developing and implementing test strategies, Maintaining and advancing the portfolio of projects, Providing technology planning/IT roadmapping, information security advisory services, and cyber resilience planning across the WPO, Collaborate with Service Delivery Organizations to provide technology excellence in support of the Fedwire Services, Develop and execute comprehensive test plans, test cases and execution scripts for highly complex Fedwire® business lines (over 40 applications), Review test output and document results including logging and following up on identified problems, Utilize an end to end test management toolset (Silk Central), covering test validation linkage to its requirement, Develop a thorough understanding of all Fedwire® applications, interfacing applications, statements and reports, Key contributor to the development of business and user requirements for existing and/or new Fedwire® applications, Key contributor in recommending best solutions in achieving the business objective, May assist in the development of user training material; train various users (Wholesale Operating Sites, Wholesale Testing Unit users, and Backup Production Operations support team, Provide Fedwire® business operations and production support (including off hours and weekend support), Work closely and collaborate with various project and operations stakeholders across Federal Reserve System, Support multiple concurrent initiatives occurring in numerous environments across all Fedwire® Business lines, Develop strong relationships across all QA Testing Teams and negotiate QA environment schedules for competing time critical projects and ongoing maintenance activities, Coordinate and support production implementation of all environmental and application changes to the Fedwire® applications to meet business production high availability requirement. Preparation & review of Tech transfer Protocol and Report. Supriya pravin patil. Inspects materials, reviews batch records for completeness and accuracy of entries, assesses the adequacy of investigations of deviations and verifies the conformance of test results with the established standards, Assists with the review and approval of all quality documentation e.g. When hunting for a quality assurance job, having a great resume or CV with an irresistible objective statement can increase your chances of being invited to an interview. Compilation ANDA / Dossier and submission of annual updates for ANDA / Dossier. Tips for writing your resume . sterilization, raw materials inspection, document control, maintenance and calibration, environmental monitoring and control, manufacturing, engineering, etc. Objective: Seeking middle level assignments in Regulatory Affaires/ Quality Assurance/ Quality Control with a reputed organization in the Pharmaceutical Sector. Quality Control Manager Resume Example Leading Pharma. Must protect the confidentiality of sensitive information in the department. Based on the most successful resume samples, these experts should demonstrate quality assurance expertise, attention to details, leadership, organizational skills, and … Keywords: Quality assurance CV template, relevant work experience, quality management, compliance activities, training needs, recommendations, QA skills Created Date: 1/1/2004 12:49:43 AM Responsible for identifying deviations in the processes that ensure all activities are cGMP compliant, identifying corrective actions, assisting with RCA, establishing path forward activities and appropriate documentation is complete. Areas of expertise include Process Improvement, QMS, SPC and Metrics and Auditing. Knowledgeable of quality control standards, Conditioning and quality procedure expertise. Responsible for specific project work such as process improvement/remediation and maintain ownership and responsibility for specific QA processes. Pharmaceutical expertise with relevant qualifications plus hands We always effort to show a picture with high resolution or with perfect images. compliance to dress code, Bell collateral, etc. 19.4 PROCuReMeNT however, in a resource-constrained setting, the risks to patients … Analyze trends and generate reports/updates from these databases, May be required to conduct external vendor audits, May be required to attend off-campus training or COH training seminars, Masters of Science with 0 – 4 years of experience, preferred, Manage Vendor Qualification System Audit vendors: coordinate travel, audit, and provide audit reports to the vendor, Manage controlled substance activities: ordering and completing DEA 222 forms; receive, log, issue controlled substances for laboratory testing, and maintain logbooks, Manage the Product Complaint process: intake, process, investigate, and trend complaints, Speak with patients and follow-up with vendors, physicians, pharmacists, etc, Route manufacturing and quality documentation to vendors and management, Initiate, review and route deviations and non-conformance documents, Issue, review, and approval Change Controls CCs related to all controlled documents, Perform QA document review on manufacturing and quality documents, Establish training for other departments and directly train employees in other departments, Write, review, and revise SOPs, protocols, etc, Responsible for the QA/QC content review of clinical trial-associated documents for new and ongoing programs, Bachelor’s Degree in Science or related field (preferred), 5+ years’ experience within Clinical Quality Assurance. Quality Assurance Manager. Resume: PRIYA SINGH PARIHAR. No need to think about design details. A quality assurance resume example better than 9 out of 10 other resumes. Stay up to date with all Flightpath system changes. degree and 0- 3 years’ experience in pharmaceutical manufacturing or 4-8 years of equivalent experience, Undergraduate degree in engineering, scientific, business or QRC disciplines. Providing hands-on coordination and support for execution of the nonconforming product (NCR) process and corrective and preventive actions (CAPA), Working and communicating with the QA and non-QA organization across MPD to support a quick and robust decision-making process in support of quality system requirements, Supporting prioritized activities, including NCR, CAPA, FIR and operational improvements, Helping manufacturing with daily issues related to quality system requirements, Training and educating others on quality-system requirements and good documentation practices to help ensure compliance, Advising and working with various teams (e.g. Create your resume now . A.) Enhancv is a simple tool for building eye-catching resumes that stand out and get results. Also note how the quality assurance specialist resume template for Word utilizes strong action verbs at the beginning of each line. - Choose from 15 Leading Templates. Assist with dispatch when needed, Advanced typing and computer skills – MS Office (including Excel, Word, Outlook, etc. Previous working experience in a lab is preferred, Demonstrated cGMP knowledge and experience is required, Previous experience implementing Quality Systems (CAPA, Root Cause Analysis, Change Management, Deviations, Inventory Management), Demonstrated experience of working collaboratively in a team environment is required, Strong analytical skills, detail-oriented, Demonstrated experience meeting critical deadlines; maintaining precision and accuracy and performing under pressure, Japanese level 2 or similar, can fluently read, write and have phone call in Japanese, Open-minded, easy-going, reliable, patient, positive working attitude, good sense of responsibility, Good Aesthetic judgment, be able to understand the meaning of images displaying; good cognition of product shape and pattern, Familiar with Photoshop software at elementary level, Experienced in QA in an E-commerce company is preferred, Have customer support experience is preferred, Good command of Excel and experience with using Excel as basic analysis tool is preferred, Good command of written English is preferred, Perform ongoing formal testing of completed KYC records to ensure standards are met, Review the quality of completed KYC records using pre-defined test scripts which are based on KYC and Quality Assurance standards, Question and investigate the reliability and integrity of data, the validity of conclusions and the appropriateness of assumptions made (where appropriate), Present findings via formalized feedback loop process, track and monitor corrections to identified critical defects, Effectively communicate with key points of contact to ensure the fluid sharing of information and feedback across pertinent teams, 5+ years of experience with Financial Services industry, AML/BSA, KYC, Sanctions, Compliance, Investigative or Quality Assurance background preferred, Demonstrated experience adhering to controls and compliance standards, Working knowledge of MS office & MS SharePoint, Strong knowledge of customer care processes and techniques, Projects positive team image and demonstrated ability to work well in a team environment, Understands and maintains confidentiality of information and results, Requires moderate to intense concentration due to complexity and/or need to meet deadlines, and flexibility to readily adapt to a changing environment, Functioning knowledge of Microsoft systems including: Word, Excel, Ability to meet deadlines in a fast-paced work environment driven by software systems and processes, Ability to trouble-shoot and make visual quick decisions based on training, Authorized to work in the U.S. without sponsorship, Ability to multi-task & prioritize, with strong organizational and follow-up skills, Attending and participating in applicable company-sponsored training, Ability to work in group setting and independently; ability to adjust to changing priorities, Excellent attention to detail and orientation toward meticulous work, 3+ years relevant experience in areas of Quality Assurance, Inspection, or Auditing, Possesses a strong working knowledge of Good Clinical Practices (GCP), Quality/Regulatory Guidelines, and is competent with quality control procedures including acceptance criteria, Computer literate and familiar with most common software applications (i.e., Word, Excel etc. Change management, negotiation, conflict resolution, and collaboration with others users, Nikos, had this say... Environment and fully understand the importance of such jobs we have collected a few Assurance! United States and procedures and also monitor constantly that the produced goods/service meet agreed! Tech transfer Protocol and Report production problems and operational issues to Preferred.. ; About ; Blog ; Contact ; resume samples to use to create your own with... Qa-Qc Welding Inspector or Qa-qc Mechanical Engineer develop skills to achieve compilation ANDA / and! Add your Accomplishments own resume with our easy-to-use resume builder reviews and approves responses and corrective action identification through use. And operational issues to senior management and supervisory personnel from Operations quality control resume. Tools ( i.e some examples of a well-written work experience section contribute to content. With over 10 years of QA /QC experience in Pharma/Biotech/Clinical by Expert recruiters tailor your resume to Indeed resume get. 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