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Strong Philips brand, mid-level QA title, metro Bangalore location, and 5–7 year range increase competition.
Role requires medical-device regulatory and post-market quality expertise, limiting transferability across industries.
Mandatory 5–7 years, regulatory medical-device expertise, and preferred ISTQB make filters stringent.
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Maintain and develop comprehensive software quality documentation ensuring compliance with standards and regulations throughout the software lifecycle.
Assess software designs and conduct root cause analysis to ensure quality, safety, and regulatory compliance, embedding quality in design and addressing deficiencies.
Oversee execution of software quality plans, risk management, and post-market performance monitoring, providing feedback and initiating corrective actions as required.
Bachelor's Degree in Computer Science, Computer Applications, or equivalent/vocational education.
5-7 years of experience in Software Quality Engineering.
Knowledge of global regulations and standards relevant to software quality and regulatory compliance.
Onsite role requiring full-time presence at company facilities.
Experienced in design quality management, root cause analysis, CAPA methodologies, and regulatory compliance in software development.
Skilled in software lifecycle quality activities including quality plans, risk management, and post-market analytics.
Capable of mentoring and guiding quality engineering practices aligned with business and regulatory objectives.