Regulatory Affairs Job at Radiometer | Pharma Graduates Apply Now
Radiometer (a Danaher company) is hiring a Regulatory Affairs Professional, Database for its Commercial QA/RA team. This Regulatory Affairs Job is based in India. The role focuses on managing regulatory databases to ensure audit readiness, accurate product records, and compliant global registrations. Ideal for professionals skilled in data validation and regulatory archiving, this position offers the opportunity to drive impact within the life sciences and diagnostics sector.
- Job Role: Regulatory Affairs Professional
- Location: Hyderabad
About Radiometer
Radiometer, part of Danaher’s 15+ operating companies, is dedicated to innovating for a tangible impact. Our work in life sciences, diagnostics, and biotechnology saves lives, and we are united by a vision to improve global healthcare through reliable, fast, and easy patient diagnoses. We foster a culture of belonging where your unique viewpoint matters, driving us forward in improving patient care. Learn about the Danaher Business System, which makes everything possible.
Job Description
The Regulatory Database Professional is responsible for managing a regulatory database to ensure audit readiness, accurate records, compliant registrations, validated data, archiving, and user training/support. This position reports to the Senior Manager Commercial QA/RA and is part of the Commercial QA/RA team, and will be a remote role in India.
Responsibilities
- Manage and keep the Regulatory database audit-ready, and maintain accurate product records.
- Handle intake of registration requests and coordinate timely follow-up actions.
- Monitor compliance progress to ensure updates are completed on time and meet regulatory standards.
- Verify accuracy of entries and archive documentation per company and regulatory procedures.
- Provide training and ongoing assistance to ensure effective and compliant database use.
Requirements
- Master’s degree, e.g., pharmaceutical sciences, medical technology, or a similar science field is required for the Pharma Job.
- Experience in Regulatory Affairs within the medical device or diagnostics industry.
- Proficiency in regulatory systems/tools (e.g., electronic submission platforms, document control systems).
- Familiarity with global regulatory frameworks and product registration processes within life sciences.
- Ability to interpret and apply global regulatory requirements (EU MDR, IVDR, FDA, Health Canada, PMDA, etc.).
