Designs, develops, evaluates, and conducts integration, Automated testing, and verification activities of (elements of) products with focus on mechanical, electrical and (embedded) software aspects and concludes this with formal reporting. Defines, implements, and maintains reliable and reproducible testing methodologies and equipment, ensuring compliance with quality requirements.
Job Description
Lead system testing & Automation activities on regulated medical devices
Applies comprehensive knowledge of software quality concepts within the software development lifecycle
Perform in-depth impact analysis of the system and requirement
Provide the effort estimation for the responsible area
Develop test plans and strategies on the responsible area
Drive the implementation of test plans and test strategies
Lead test case development and peer review process on the responsible area
Lead test case execution process and generate test reports on the responsible area
Drive STE deliverables to meet project schedule
Train and mentor other testers on automation as Subject Matter Expert (SME)
Provide weekly status update to management on team progress
Participate in project core team meetings
Participate in design & code reviews and technical documentation reviews
Drive the automation work within the team & aim to achieve committed automation coverage
Provide status update to management on overall test and automation progress
Role Competency:
Bachelor's degree in engineering or other relevant discipline
9+ years of experience on test discipline, test strategy, test automation
Prior experience of playing the role of test lead is preferred
Hands on Experience with automation framework development is preferred
Experience in healthcare product /System testing is preferred
Very strong Programming skills (preferably C#) is required.
Good experience on automation tools, scripting languages is required
Experience with BDD, Gherkin, Specflow is a must.
Strong experience in application life cycle management tools like ALM/PTC/TFS used for Verification activities
Good understanding of the defect management procedures and tools.
Good understanding of configuration management & related tools is required.
Expertise in test strategy, test design skills and able to guide the team on these.
Strong knowledge on the healthcare standards and its relevance to verification and validation activities.
Good understanding/experience of the healthcare/Interoperability standards is advantage.
Good knowledge in DICOM, ISO and IEC standards is required.
Possess strong regulatory knowledge(Ex: FDA, 510K etc)
Personal Characteristics:
Excellent communication and documentation skills
Openness to collaborate in interest of project/organization.
Proactive and self-driven, possesses due sense of urgency
Shall be very good technically; possess systems mindset and good problem solving abilities.
Working with multisite teams, Quality conscious and & customer Oriented
Why should you join Philips?
Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on improving 3 billion lives a year by delivering innovative solutions across the health continuum. Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways.
To find out more about what it’s like working for Philips at a personal level, visit the Working at Philips page on our career website, where you can read stories from our employee blog. Once there, you can also learn about our recruitment process, or find answers to some of the frequently asked questions.