Medical Job at Radiometer – Apply Now
Medical Job: Radiometer, a global leader in medical diagnostics and part of the Danaher Group, is hiring for a Regulatory Affairs Professional – Database role. This regulatory affairs job offers an excellent opportunity for experienced professionals to work remotely from India while contributing to life-saving medical device and diagnostics solutions used worldwide.
Medical Job Details
- Job Title: Regulatory Affairs Professional – Database
- Location: Remote (India)
- Employment Type: Full-time
- Work Mode: Remote
- Industry: Medical Devices / Diagnostics / Life Sciences
- Reporting To: Senior Manager – Commercial QA/RA
About the Company
Radiometer, founded in 1935 and headquartered in Copenhagen, Denmark, is a pioneer in acute care diagnostics, best known for innovations in blood gas testing. Today, Radiometer’s solutions are used in hospitals, laboratories, and clinics across 130+ countries, helping clinicians make fast, accurate diagnostic decisions that improve patient outcomes.
As a proud member of the Danaher Group, Radiometer operates within a culture of continuous improvement driven by the Danaher Business System (DBS), enabling innovation at scale while maintaining the highest standards of quality, compliance, and patient safety.
Medical Job: Eligibility & Qualifications
- Master’s degree in medical technology or a related science discipline
- Prior experience in Regulatory Affairs within the medical device or diagnostics industries
- Hands-on experience with regulatory systems, document control tools, or submission platforms
- Working knowledge of global regulatory frameworks such as EU MDR, IVDR, FDA, Health Canada, PMDA, etc.
- Strong attention to detail and a regulatory compliance mindset
About the Role
The Regulatory Affairs Professional – Database role focuses on managing regulatory databases to ensure audit readiness, data accuracy, compliant product registrations, and validated regulatory records. This position plays a critical role in supporting global regulatory operations by maintaining high-quality regulatory data, supporting compliance activities, and enabling smooth regulatory workflows across regions.
This regulatory affairs job is ideal for professionals with experience in medical devices or diagnostics, strong regulatory system knowledge, and familiarity with global regulatory frameworks.
Key Responsibilities
- Maintain regulatory databases with accurate, compliant, and audit-ready product records
- Manage intake and tracking of regulatory registration requests
- Monitor regulatory compliance progress and ensure timely updates
- Verify database entries and archive regulatory documentation per procedures
- Provide user training and ongoing database support
- Support global regulatory readiness across multiple markets
- Collaborate with QA, RA, and commercial stakeholders
