Table of Contents
Philips Careers | Regulatory Affairs Specialist Bangalore
Are you ready to make an impact in global health technology? Philips Careers is offering an exciting opportunity for a Regulatory Affairs Specialist in Bangalore, where innovation meets purpose. This life science job in Bangalore is ideal for professionals eager to ensure regulatory excellence, drive product compliance, and contribute to a company transforming healthcare worldwide. Join Philips Bangalore Careers and take your expertise to a place where every contribution matters.
Job Details:
- Job Position: Regulatory Affairs Specialist
- Location: Bangalore, India
- Job ID: 562991
- Application Deadline: November 5, 2025
About the Company:
At Philips, we’re committed to improving lives through meaningful innovation. As a global leader in health technology, our mission is rooted in the belief that every person deserves quality healthcare. Through collaboration, care, and innovation, Philips Careers empowers professionals to shape a healthier future for communities worldwide.
Qualifications:
- Education: Bachelor’s Degree in Biomedical Engineering, Quality Management or related field.
- Experience: Minimum 2 years with vocational education in regulatory or quality-related roles OR no experience required for candidates with a Bachelor’s degree.
- Certifications: Not mandatory but preferred for advanced regulatory fields.
About the Role to Enhance your Philips Careers
This Regulatory Affairs Specialist role in Philips Bangalore Careers offers an exciting opportunity to work at the forefront of medical device compliance and global regulations. You will collaborate with cross-functional teams to ensure Philips products meet international quality and safety standards. From developing strategies to managing documentation, this role contributes directly to the company’s mission of improving lives through innovation.
Job Description:
- Support the company’s global regulatory strategy and ensure compliance with international standards.
- Prepare, review, and submit documentation for regulatory approvals.
- Collaborate with product development, supply chain, and quality management teams to meet compliance goals.
- Stay current with evolving global regulations in the medical device and life science sectors.
Key Responsibilities at Philips Careers:
- Develop regulatory strategies for assigned products.
- Ensure all documentation aligns with health authority requirements.
- Participate in audits, risk assessments, and continuous improvement initiatives.
- Support product lifecycle management and regulatory submissions across regions.
