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Philips brand and Bangalore location increase competition, but medical-device regulatory specialization reduces the applicant pool.
Medical-device quality and regulatory expertise strongly limits cross-industry transferability.
Explicit 5-7 years requirement and regulated medical-device quality expertise make hiring filters stringent.
Develop and maintain comprehensive software quality documentation ensuring compliance with standards and regulatory requirements throughout the software lifecycle.
Assess software designs by reviewing test and performance data to ensure quality, safety, and regulatory compliance, while identifying and resolving quality deficiencies.
Monitor software performance using post-market analytics, guide risk management and quality plan execution, and report key software quality metrics to stakeholders.
Bachelor's Degree in Computer Science, Computer Applications or equivalent/Vocational Education.
5-7 years of experience in Software Quality Engineering.
Knowledge of regulatory requirements and quality standards relevant to software lifecycle.
Onsite role requiring presence in the company facilities at least 3 days per week.
Experienced in quality management and compliance within software development environments, with a strong understanding of product lifecycle and regulatory standards.
Capable of conducting root cause analysis and implementing CAPA to improve software design and quality processes.
Skilled in creating and executing design verification and validation plans aligned with business objectives and regulatory demands.