Boston Scientific Engineer Sr Test HRD 

Costa Rica, Heredia 

397488175

Costa Rica-Heredia

About the role:

Key responsibilities:

• Design, develop and execute test cases to ensure the quality of the product by proving system functionality, verify business and user requirements are met in Electrophysiology domain area.

• Manual execution of tests or execute automated test scripts.

• Ensure that tests have been conducted in accordance with written procedures.

• Document test results and write test reports.

• Diagnose problems and report bugs and enhancements in a bug tracking system.

• Provide technical guidelines, share knowledge, and demonstrate product areas to other team members on ad hoc basis.

• Acting as test lead for projects in determining test methodology, test strategy and test data setup.

• Participate in daily scrum meetings, product review meetings, bug triage meetings etc.

• Work closely with software development team, hardware engineering team, field support team, and other cross-functional teams.

What we’re looking for:

Basic Qualifications:

• Bachelor’s degree along with 7+ years of software test engineer or related experience or 5+ years with a master’s degree or advanced degree, preferably BS/MS in Computer Science, Biomedical Engineering, or equivalent.

• In-depth knowledge of software development life cycle and test methodology.

• Strong written and verbal communication skills.

• Strong analytical and problem-solving skills.

• Desired English level: C1+ 90 - 99%

• Please submit resume in English

Preferred Qualifications:

• A strong product quality and test lead experience preferably in medical device domain.

• A natural attention to detail and a penchant for organizing and documenting.

• A good learner who can master complex software and quickly adapt to new tools and technologies.

• Experience working in Agile Scrum development environment.

• Ability to think logically and analytically in a problem-solving environment.

• Ability to work independently as well as work collaboratively as part of a team.

• Demonstrated experience communicating both technical and non-technical information across teams and departments.

• Follow company policy regarding ISO and FDA documentation and compliance for medical device