Software Validation Engineer (Medical Devices)

Our client is a German global leading Medical devices manufacturer and they are looking for a**Software Validation Engineer** for their manufacturing facility in Tijuana, B.C.- Design and develop test plans, procedures and generate test reports.- Develop and execute automation scripts.- Assist developers in debugging customer issues.- Maintain/update defects database with a defect tracking system.- Support determining root cause of defects through structured analysis- Manage validation schedules based on project demands.- Participates in requirements reviews, design reviews, and related activities in development process.- Design and maintain test infrastructure for automation test suites.- Manage validation activities assigned to offshore team.**Skills Required**:- Strong communication and problem solving skills.- Self-motivated, work well in a team as well as independently.- Experience in Software development.- Knowledge in developing automation test scripts with Python.- Knowledge of MatLab and Microsoft Office.- Knowledge of SCRUM methodology & AGILE SDLC (Software Development Life Cycle)- Methodologies, tools and processes of Quality Control for software- Test Scripts/FAT SAT UAT/White Box Testing/ Black Box Testing/ Lab View / SQL Server data base design and systems.- FDA, CMDR, QSR, ISO 13485 & MDD (European Medical Device CE).- Familiar with Lean process.- Project Management skills**Education & Experience**- BS or MS in Electrical Engineering or Computer Engineering (preferred)- At least 5 years of relevant experience- Must be fluent in both Spanish and English. Strong capability with English language (verbal and written) to allow effective communication directly with staff at R&D, suppliers and customers (highly technical discussions)