Regulatory Affairs Job Opportunity for M Pharmacy Graduates at Radiometer | Apply Now
Regulatory Affairs Job opportunities are now available through Radiometer Careers, offering an excellent Pharma Job opportunity for professionals. This Regulatory Affairs Job allows candidates to work remotely in India while contributing to global healthcare innovation. If you are searching for a Pharma Job where you can manage regulatory databases, ensure compliance, and support regulatory processes in the diagnostics industry, this Regulatory Affairs Job at Radiometer could be the perfect career opportunity.
- Job Title: Regulatory Affairs Professional, Database
- Location: India
About the Company
Radiometer, one of Danaher’s 15+ operating companies, operates in life sciences, diagnostics, and biotechnology with a mission to improve global healthcare through reliable, fast, and easy patient diagnoses. The company focuses on delivering diagnostic solutions that help healthcare professionals make faster clinical decisions and improve patient outcomes.
Job Description
In this role, the Regulatory Database Professional will manage the regulatory database to ensure accurate product records, compliant registrations, and audit readiness. The role also involves maintaining validated data, archiving documentation, and providing training and support to users.
Key Responsibilities
In this Regulatory Affairs Job, you will have the opportunity to:
- 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.
Qualifications
The essential requirements of the job include:
- Master’s degree in pharmaceutical sciences or a similar science field.
- 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.)
