Automation Engineer

About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
Career development with an international company where you can grow the career you dream of.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This is a role based in Bogotá (Colombia).
The Software QA/Test Analyst will support Abbott Medical Device IT by ensuring the quality, reliability, and regulatory compliance of Digital delivery solutions. This role focuses on validating system changes, integrations, and configurations in a regulated medical device environment, supporting business operations, quality, and compliance objectives

What You’ll Do

• Execute and support on-time completion of Quality Engineering deliverables: test plans (manual), test scripts (manual & automated), test reports

• Support Design and development of test automation frameworks, as needed (mostly for web and OTA applications)

• Support on-time execution of Quality Plans

• Support Design Verification and Validation test planning & execution, including active cross-functional root-cause analysis investigation & resolution activities

• Support product Risk Management activities

• Support internal & external audit and related responses

• Support the establishment of objective, measurable and verifiable customer and product requirements

• Support all Company initiatives as identified by management and in support of Quality Management

• Build and maintain successful cross functional relationships with internal departments such as R&D Engineering, Operations, Quality, Clinical and Regulatory Affairs

• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors

• Ensure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps

• Create and manage testing schedule and work plan

• Complete Document Change Request Reviews in a timely and objective manner.

• Reviews test protocols and test results provided by another functional group

• Participate in reviews for System and Software requirements, Software and Firmware design, and code inspection, using static testing and TDD practices

• Improve implement quality tools that improve the software design reviews and implement testing tools that improve the software testing lifecycle.

Required Qualifications

• Associate's degree

• Overall 5 years

• Medical device industry 1-2 years

• Knowledge in the areas of Design Controls, Verification & Validation activities, Software practices or processes

• Experience authoring Test Cases/ Lead of test or validation effort with Software (5+ years)

• Leading of user testing acceptance

• Experience authoring and performing the testing

• TOSCA experience and knowledge.

Apply now
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
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