Join a leading medical device company as a Regulatory Affairs (Digitization) Engineer Intern in Bangalore. This internship offers hands-on experience in regulatory data management, digitization, and automation for global compliance in the pharma and medtech sector. Perfect for engineering and data science students seeking pharmaceutical careers in India.
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About the Company
ResMed (NYSE: RMD, ASX: RMD) is a global leader in digital health and medical devices, pioneering innovative technologies for sleep apnea, COPD, and respiratory care. Headquartered in San Diego with roots in Australia, the company operates in over 140 countries and empowers millions to live healthier lives through cloud-connected devices, AI-powered solutions, and intelligent software. ResMed is known for its strong focus on regulatory compliance, innovation, quality systems, and transforming home healthcare.
Job Details
- Company Name: ResMed
- Position: Regulatory Affairs (Digitization) Engineer- Intern
- Qualification: Pursuing Bachelor’s or Master’s in Engineering, Data Science, Biomedical Science, or related technical discipline
- Location: Bangalore, India
- Work Type: Full-time Internship (On-site)
Job Description
ResMed is hiring a motivated intern to support digitization and data management initiatives. This role focuses on enhancing regulatory compliance, data quality, and operational efficiency in a highly regulated medical device environment.
- Regulatory Affairs (Digitization) Engineer- Intern Department: Regulatory Affairs
- Location: Bangalore, India
- Role: Internship (Digitization & Data Operations)
- Experience: Current students / Freshers (0 years)
- Education/Qualification: Pursuing Bachelor’s or Master’s in Engineering, Data Science, Biomedical Science, or related field
Skills/Qualifications
- Currently enrolled in a relevant Bachelor’s or Master’s program
- Hands-on exposure to data manipulation tools such as Excel, Power Query, SQL, Python, R, or similar
- Strong attention to detail and ability to handle structured and unstructured data
- Interest in medical devices, regulatory affairs, quality systems, and compliance-driven processes
- Preferred: Interest in automation, dashboards, AI tools, or process improvement in regulated environments
Key Responsibilities
- Support regulatory data structuring, cleaning, and preparation for uploads
- Use Excel, Power Query, SQL, and Copilot for bulk data handling and analysis
- Perform data validation, reconciliation, and quality checks
- Assist in developing dashboards, trackers, and digital tools for regulatory visibility
- Document workflows, data standards, and process improvements
Benefits/Perks
- Valuable industry exposure in medical device regulatory affairs
- Hands-on learning with advanced data tools and automation technologies
- Supportive work culture focused on innovation and excellence
- Opportunity to contribute to global compliance projects
- Professional development and potential for future career growth at ResMed
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the ResMed career page.
🔗 Click below to apply directly for this job
Interested candidates can apply directly through the official ResMed Career Site. Search for job requisition ID JR_050042 on the ResMed careers portal.
Visit: ResMed Careers
For more pharma jobs and medtech internships across India, explore opportunities on Pharma Recruiter. Apply promptly as these positions fill quickly.
Why You Should Join
ResMed offers a dynamic, innovation-driven environment where interns work on meaningful projects that impact patient lives worldwide. You’ll gain practical experience in regulatory digitization while benefiting from a culture that values diversity, excellence, and professional growth. This internship provides excellent long-term career stability in the fast-growing medical devices and digital health sector.
FAQs
Q1: Who is eligible for the Regulatory Affairs Intern position at ResMed Bangalore?
A: Students currently pursuing Bachelor’s or Master’s in Engineering, Data Science, Biomedical Science, or related fields with data handling skills.
Q2: Is prior experience required?
A: No prior full-time experience is needed. Exposure to Excel, SQL, or Python is preferred.
Q3: What is the work location and type?
A: The internship is full-time and based in Bangalore, India (on-site).
Q4: How does this internship support pharmaceutical careers in India?
A: It builds strong foundations in regulatory compliance, data management, and quality systems — highly valued skills in pharma, medtech, and QA/QC roles.
