Talworx is an emerging recruitment consulting and services firm, we are hiring for our client which is a leading precision medicine company focused on guarding wellness and giving every person more time free from cancer. Founded in 2012, we're transforming patient care by providing critical insights into what drives disease through its advanced blood and tissue tests, real-world data and AI analytics.
Job Description
We looking for an energetic and passionate Senior Software Quality Engineer to join
its Software Engineering team. This team is responsible for delivering the product functionality
needed to support the laboratory workflow for several of its market leading cancer diagnostic tests
as well as integration with various oncology systems.
An Ideal candidate would have experience working in a regulated environment with thorough
knowledge of Quality Engineering best practices and technical expertise to deliver software products
meeting the business needs in an efficient and fast paced environment. This role requires someone
who is adept at understanding system architecture, design, implementation to succinctly develop
tailored test strategy and deliver quality software products meeting regulatory standards. The
candidate should have the aptitude to work on parallel projects with overlapping schedules, quickly
learn new technologies, demonstrate teamwork and technical leadership.
Essential Duties and Responsibilities:
β Design and execute test coverage for various functional and integration aspects of the
Enterprise Lab Information Management System (LabVantage).
β Apply appropriate test methodologies including but not limited to writing test plans, test
cases, and execution of test scripts within the sprint schedule.
β Create automated test cases and execute them to support scheduled releases.
β Troubleshoot issues identified during testing and report defects; able to distinguish between
user error and application anomalies.
β Perform System Integration and performance testing prior to product releases.
β Provide clear and concise feedback on defects, usability, and other test findings/results.
β Contribute to the continuous improvement of QA processes and methodologies.
β Collaborate with cross-functional teams to ensure timely and robust execution of testing as
part of a regular release schedule.
β Provide coaching to other team members for designing test strategies and test cases.
β Execute complex testing scenarios, perform in-depth statistical analysis, and interpret results
independently.
β Apply QE standards, best practices, and principles to develop quality plans that deliver
optimal outcomes across multiple products.
β Deliver test documentation to support software development for medical devices in
compliance with FDA, IVDR, CE mark, IEC 62304, PMDA and ISO 13485 standards.
β Stay updated on industry best practices and emerging technologies relevant to software
quality assurance in life sciences.
Qualifications:
β B.S or higher degree in Computer Science, Engineering, Bioinformatics, or a related study or
equivalent project experience.
β 8-10 years of hands-on testing experience in Service Oriented Architecture environment using
COTS/SaaS solutions with API led integrations.
β Solid experience in programming languages like Java, Python
β 5+ years of experience in testing integrations in a hybrid environment leveraging
XML/JSON/HL7 message formats.
β 5+ years of experience using databases like Postgres, Oracle, MSSQL Server or Mongo DB.
β 5+ years of experience in test preparation activities within an Agile Development Process β
Test Design, Test scripting, Test Data creation.
β 5+ years of API test tools like Postman, Fiddler, RestAssured, SOAPUI, JMeter required.
β Develop test automation scripts to support CI/CD pipeline for software delivery.
β Proven ability to adapt to new technologies and design test strategies.
β Extensive experience in good testing practices, QA methodologies, tools, and processes.
β Excellent communication, presentation, and analytical skills, including strong ability to
identify and solve ambiguous cross-functional software quality related problems.
β Expertise in measuring and reporting quality-related metrics to identify trends, anomalies and
proactively resolve problems.
β Experience in identifying, analyzing, and narrowing down system integration issues and
performing root cause analysis.
β Expertise in developing and maintaining SDLC documentation such as Verification Plan,
Report, Validation Plan, Risk Assessment, and Traceability Matrix, etc.
β Ability to deliver software releases in frequent cycles using agile methodology.
Β Desirable, but not Required:
β 3+ years of performing verification and validation activities in medical device, pharma or
healthcare regulated environments.
β Experience working in a regulated environment (CLIA, CAP, HIPAA, SOX, 21 CFR Part 11,
ISO 13485, IEC 62304, and other FDA regulations)
β Working experience in MuleSoft platform.