Philips Hiring Data Analyst

Data Analyst | Life Sciences Graduate | Philips Bangalore

Philips is hiring a Data Analyst in Bangalore. Bachelor’s in Life Sciences, 4-8 yrs post-market surveillance experience, Medical Device focus.

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Bangalore-based professionals with a passion for healthcare innovation, here’s your opportunity to join Philips as a Data Analyst. Be part of a team driving post-market surveillance, data analytics, and operational excellence in the medical device domain. If you thrive in structured yet collaborative environments and have experience in FDA/EU-MDR regulated products, this role is designed for you.

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Company Overview

Philips is a global leader in health technology, striving to improve the lives of 3 billion people annually by 2030. With innovations spanning diagnostic imaging, patient monitoring, cardiology, sleep therapy, and respiratory care, Philips empowers healthcare providers to deliver confident diagnosis and care.

The company fosters a culture of innovation, collaboration, and employee growth. Its hybrid work model balances flexibility with team collaboration, offering employees the ability to contribute meaningfully while maintaining a healthy work-life balance.

Learn more at www.philips.com

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Job Role & Responsibilities

As a Data Analyst at Philips, you will execute critical post-market surveillance and data management activities, ensuring compliance with global medical device regulations. Key responsibilities include:

• Execute low-complexity post-market surveillance processes within predefined guidelines, ensuring efficiency, quality, and consistency.

• Develop and deliver comprehensive reporting tools for informed decision-making across clinical operations and business functions.

• Conduct quality assurance on communication tools and reporting documents to ensure accuracy, efficacy, and regulatory compliance.

• Collaborate with business process experts to design and deliver training programs for process enhancement and knowledge transfer.

• Gather, merge, and analyze data from multiple sources to support risk assessment, performance monitoring, and strategy implementation.

• Document and maintain meticulous records of post-market surveillance activities for monitoring product safety and compliance.

• Compile and analyze continuous product performance data to identify safety trends, deviations, or potential risks.

• Support the preparation of regulatory post-market surveillance documentation, including plans and reports, in alignment with FDA/EU-MDR guidelines.

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Eligibility / Qualifications

Essential Requirements:

• Bachelor’s degree in Life Sciences, Biomedical Engineering, Medical Sciences, Healthcare Management, Industrial Engineering, or related fields.

• 4-8 years of post-market surveillance experience in FDA/EU-MDR regulated medical device environments.

• Strong knowledge of medical device regulations, including 21 CFR Parts 803, 806, 820, ISO 13485, ISO 14971, EU MDR, and Canadian Medical Devices Regulation (SOR/98-282).

• Proven ability in data analysis, reporting, and quality management.

• Excellent written and oral communication, stakeholder management, and collaboration skills.

• Experience in post-market surveillance plans/reports, risk assessment, and continuous product performance analysis.

Preferred Skills:

• Device Recall Procedures and QMS management.

• Regulatory documentation and compliance understanding.

• Training delivery and process improvement expertise.

• Business intelligence tools, data management, and project management skills.

• Product knowledge in Diagnostic X-rays preferred.

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Location & Work Model

• Location: Bangalore, Karnataka, India

• Work Type: Full-Time, Hybrid (3 days office / 2 days flexible remote)

• Philips promotes collaboration and innovation through in-office presence while offering flexibility to maintain work-life balance.

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Application Process

Interested candidates can apply directly on Philips career portal.

• Ensure your profile is updated with relevant experience and education.

• Upload a professional resume highlighting your post-market surveillance expertise and medical device knowledge.

• Applications close on October 21, 2025 – apply early to secure your spot!

For queries, contact Philips HR via the portal for assistance.

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Why Join Philips?

• Be part of a global health technology leader with innovations in imaging, patient monitoring, cardiology, and respiratory care.

• Gain exposure to regulatory compliance, post-market surveillance, and cutting-edge data analytics in medical devices.

• Work in a hybrid, flexible, and collaborative environment designed for employee well-being and professional growth.

• Competitive salary, benefits, and opportunities for career progression in a company committed to diversity, equity, and inclusion.

• Directly contribute to improving patient outcomes for millions worldwide.

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FAQs

Q1: What educational background is required?
A: A Bachelor’s degree in Life Sciences, Biomedical Engineering, Medical Sciences, or related technical fields.

Q2: How much experience is needed?
A: 4-8 years in post-market surveillance within FDA/EU-MDR regulated medical device environments.

Q3: Is knowledge of specific medical devices required?
A: Product knowledge in Diagnostic X-rays is preferred but not mandatory. Regulatory expertise is essential.

Q4: Can freshers apply?
A: This is a mid-level role; candidates must have prior post-market surveillance experience.

Q5: What is the application deadline?
A: October 21, 2025 – early applications are encouraged.

Q6: What is the work model?
A: Hybrid – 3 days in-office, 2 days flexible remote.

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