Description
Philips is hiring a Non-Product Software Validation Engineer to own and strengthen the validation and assurance framework for non-product software and computerized systems in a regulated medical device environment. The role covers the full computerized system lifecycle, including validation planning, risk assessment, testing, traceability, change control, data integrity, supplier assurance, audits, and lifecycle monitoring, while advising cross-functional teams and coaching validation personnel. The position requires a bachelor’s or master’s degree in a relevant technical or quality field and at least eight years of relevant experience in computerized systems, software quality, validation, or quality assurance within a highly regulated life sciences industry. The role is office-based and requires working in person at least three days per week.
