Vantive Careers is hiring experienced professionals for the position of Regulatory Affairs Specialist in Bangalore, Karnataka. This Regulatory Affairs job in Bangalore is an excellent opportunity for candidates with expertise in EU MDR, US FDA submissions, and global regulatory compliance within the medical devices or digital healthcare sector.
The company is seeking talented regulatory professionals who can support sustaining projects, manage global submissions, and ensure compliance for Vantiveโs growing digital healthcare portfolio. Candidates looking for Regulatory Affairs Specialist jobs in Bangalore, medical device regulatory affairs careers, or MDR compliance jobs in India should explore this opportunity.
About Vantive
Vantive is a global vital organ therapy company focused on improving patient outcomes through innovations in kidney care, dialysis solutions, and advanced digital healthcare services. With over 70 years of healthcare innovation, Vantive continues to expand its impact in vital organ therapies worldwide.
Job Details
| Particulars | Details |
|---|---|
| Job Title | Regulatory Affairs Specialist |
| Company | Vantive |
| Location | Bangalore, Karnataka, India |
| Job Type | Full-Time |
| Department | Regulatory Affairs |
| Experience | 3โ8 Years (Expected) |
| Salary | โน10 LPA โ โน18 LPA (Estimated) |
| Job ID | JR – 194199 |
| Posted Date | May 26, 2026 |
Regulatory Affairs Specialist Responsibilities
The selected candidate will be responsible for managing global regulatory activities and ensuring compliance for Vantiveโs healthcare products and digital portfolio.
Key Responsibilities:
- Develop regulatory strategies for sustaining projects and digital healthcare portfolios
- Prepare and compile regulatory dossiers for EU and US markets
- Support GeoX regulatory submissions and documentation
- Plan regulatory activities for EU MDD and MDR compliance
- Obtain regulatory approvals and clearances in target countries
- Coordinate with regulatory authorities and address deficiency responses
- Work with in-country regulatory teams for submissions, renewals, registrations, and product lifecycle activities
- Ensure adherence to global medical device regulatory requirements
Qualifications Required
Candidates applying for this Regulatory Affairs Specialist job should possess:
- Bachelorโs or Masterโs degree in Pharmacy, Life Sciences, Biotechnology, Biomedical Engineering, or related fields
- Experience in medical device regulatory affairs or digital healthcare regulations
- Knowledge of EU MDR, MDD, US FDA, and global submission processes
- Strong understanding of regulatory documentation and compliance
- Excellent communication and stakeholder management skills
- Experience coordinating with international regulatory agencies is preferred
Preferred Skills
- EU MDR compliance expertise
- US FDA submission experience
- Regulatory strategy planning
- Medical device lifecycle management
- Digital healthcare regulations
- Global regulatory submissions
- Documentation and dossier preparation
Why Join Vantive?
Working at Vantive offers professionals an opportunity to contribute to life-changing healthcare innovations while building a strong global career in Regulatory Affairs.
Employee Benefits:
- Competitive salary package
- Exposure to global regulatory markets
- Career growth in digital healthcare and medical devices
- Collaborative international work environment
- Opportunity to work on innovative healthcare technologies
How to Apply
