Analyst, Quality Assurance

4 weeks ago


Malvern, United States CyberTec Full time
Client: DaVita
Req # 18701839
Job Title: Analyst, Quality Assurance (IT)
Location: Malvern, PA
Duration: 6 months
(Pay Rate: $45/hr on C2C

Need only 4 year good fit candidate

Manual Testing, Database Testing for Migration to Cloud GCP/BQ Project

Duties
  • Analyzes, tests, debugs, and documents programs in middleware technology; experienced with middleware platforms
  • Agile methodology experience in creating epic stories, user stories, tasks, project plan and estimates
  • Review requirements and design documents with developers and quality assurance manager to confirm expected functionality with technical and business needs.
  • Implementation, evaluation, and documentation of the developed test cases and scenarios.
  • Determine test environment and test data requirements, often in concert with integrated systems' owners.
  • Must be able to communicate with leads regarding project readiness, status and potential risks. Document, quantify, and elevate risks as appropriate. Provide statistical reporting and analysis as necessary.
  • Assimilates information quickly, communicates complex requirements and issues clearly and concisely. Able to analyze root cause of a problem and demonstrate good sense when handing the problem over to development.
  • Tracks and coordinates defect resolution and retesting, quantifying and mitigating risk accordingly.
  • Enthusiastically collaborates with business partners to ensure DaVita Mission and Core Values are fulfilled.
  • Validating, analyzing, supporting customized healthcare system interfaces as well as providing level 3 support for associated interfaces.
  • Researching problems, testing, training and documenting best practices.
  • Working with internal application partners and external vendors on interface engine specifications and qualifying desired interfaces.
  • Compiling documentation of program development, and analyzing system capabilities to resolve questions of program intent


  • Malvern, United States Entech Full time

    We're living and working in the midst of a digital revolution, and the demand for optimized technology practices has never been more critical for businesses. At Entech, it's our mission to help companies navigate the changing environment and accelerate digital realization through the power of solutions, services, and product platforms. With comprehensive...


  • Malvern, United States Entech Full time

    We’re living and working in the midst of a digital revolution, and the demand for optimized technology practices has never been more critical for businesses. At Entech, it’s our mission to help companies navigate the changing environment and accelerate digital realization through the power of solutions, services, and product platforms. With comprehensive...


  • Malvern, United States Entech Full time

    We’re living and working in the midst of a digital revolution, and the demand for optimized technology practices has never been more critical for businesses. At Entech, it’s our mission to help companies navigate the changing environment and accelerate digital realization through the power of solutions, services, and product platforms. With comprehensive...


  • Malvern, United States AIMS International USA (AIMS-US) Full time

    OverviewThe Director of Quality is primarily responsible for overseeing the execution of the Quality Management System. This includes oversight of all quality assurance and all quality control functions. Ensuring compliance with cGMPs, policies, procedures and standards that are required to support manufacturing of active pharmaceutical ingredients and...


  • Malvern, United States AIMS International USA (AIMS-US) Full time

    OverviewThe Director of Quality is primarily responsible for overseeing the execution of the Quality Management System. This includes oversight of all quality assurance and all quality control functions. Ensuring compliance with cGMPs, policies, procedures and standards that are required to support manufacturing of active pharmaceutical ingredients and...


  • Malvern, United States AIMS International USA (AIMS-US) Full time

    OverviewThe Director of Quality is primarily responsible for overseeing the execution of the Quality Management System. This includes oversight of all quality assurance and all quality control functions. Ensuring compliance with cGMPs, policies, procedures and standards that are required to support manufacturing of active pharmaceutical ingredients and...


  • Malvern, United States Havpak Inc Full time

    Job DescriptionJob Description1st and 2nd ShiftRole Description:The Quality Control Inspector will assist the quality assurance department in implementing and supporting various GMP regulations throughout the facility with primary focus on in process inspections of manufacturing, assembly, and packaging processes.Key Responsibilities/Deliverables: Work with...


  • Malvern, United States Insight Global Full time

    Required Skills and Experience:-Bachelor's Degree required in Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsNice to Have Skills and Experience:-Clinical product experience-GMP...


  • Malvern, United States Insight Global Full time

    Required Skills and Experience:-Bachelor's Degree required in Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsNice to Have Skills and Experience:-Clinical product experience-GMP...


  • Malvern, United States Insight Global Full time

    Required Skills and Experience:-Bachelor's Degree required in Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsNice to Have Skills and Experience:-Clinical product experience-GMP...


  • Malvern, United States Insight Global Full time

    Requirements: -Bachelor’s Degree required; focused degree preferred in Engineering, Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsPreferred:-Clinical product experience-GMP Manufacturing...


  • Malvern, United States Insight Global Full time

    Requirements: -Bachelor’s Degree required; focused degree preferred in Engineering, Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsPreferred:-Clinical product experience-GMP Manufacturing...


  • Malvern, United States Insight Global Full time

    Requirements: -Bachelor’s Degree required; focused degree preferred in Engineering, Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsPreferred:-Clinical product experience-GMP Manufacturing...


  • Malvern, Arkansas, United States Johnson & Johnson Full time

    Janssen Biotech, Inc a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Assurance Associate II This position will be located in Malvern, PA. At Johnson & Johnson, we believe health is everything Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where...


  • Malvern, United States Amazon.com Services LLC Full time

    Ring is looking for a Software Quality Assurance Engineer to join a team of hands-on, passionate professionals developing innovative products. The person in this position will be responsible for qualifying products and features developed by cross functional teams; developing test plans and test cases mapping to product requirements; documenting end user...


  • Malvern, Arkansas, United States Johnson & Johnson Full time

    Janssen Biotech, Inc a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Assurance Associate II This position will be located in Malvern, PA.At Johnson & Johnson, we believe health is everything Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where...


  • Malvern, United States Insight Global Full time

    Required Skills and Experience:-Minimum of a Bachelor Degree in science or equivalent technical field-Minimum of two years of experience working within biological or pharmaceutical system management-Experience in a Quality Control setting.-Skilled in basic and advanced knowledge of LIMS systems.-Knowledge and understanding of current Good Manufacturing...


  • Malvern, United States Insight Global Full time

    Required Skills and Experience:-Minimum of a Bachelor Degree in science or equivalent technical field-Minimum of two years of experience working within biological or pharmaceutical system management-Experience in a Quality Control setting.-Skilled in basic and advanced knowledge of LIMS systems.-Knowledge and understanding of current Good Manufacturing...


  • Malvern, United States Insight Global Full time

    Required Skills and Experience:-Minimum of a Bachelor Degree in science or equivalent technical field-Minimum of two years of experience working within biological or pharmaceutical system management-Experience in a Quality Control setting.-Skilled in basic and advanced knowledge of LIMS systems.-Knowledge and understanding of current Good Manufacturing...


  • Malvern, United States iSpace Full time

    Title: Business Intelligence QA Analyst (Data Integration) Location: Malvern, PA (Hybrid 3 days onsite each month, 2 nd full week of the month on Tuesday, Weds, and Thursday and then the rest of the work will be remote. Onsite could become more frequent in the future) Duration: 3-month contract with strong possibility of an extension This QA...