Looking to start your career in Regulatory Affairs (RA)? Baxter has announced a new RA Associate opportunity in Bangalore, Karnataka, for candidates with 0–2 years of experience. This is an excellent opportunity for engineering graduates who want to build a career in Global Regulatory Affairs, medical devices, biologics, and pharmaceutical regulatory submissions.
The selected candidate will support global product registrations, regulatory submissions, lifecycle management activities, and collaborate with international regulatory teams. If you’re interested in Regulatory Affairs jobs in India, Baxter RA Associate Jobs 2026 is one of the best entry-level opportunities available.
Baxter RA Associate Job Overview
| Particular | Details |
|---|---|
| Company | Baxter |
| Job Title | RA Associate |
| Department | Global Regulatory Affairs |
| Job Type | Full-Time |
| Experience | 0–2 Years |
| Qualification | Bachelor’s Degree in B.Tech |
| Location | Bangalore, Karnataka |
| Industry | Medical Devices, Pharmaceuticals, Biologics |
| Application Deadline | 24 July 2026 |
About Baxter
Baxter is a global healthcare company committed to improving patient outcomes through innovative medical technologies, pharmaceuticals, and healthcare solutions. With operations across multiple countries, Baxter offers professionals the opportunity to work on global regulatory projects while contributing to life-saving healthcare products.
The selected Regulatory Affairs Associate will be responsible for:
- Supporting global and regional regulatory teams across multiple countries.
- Preparing regulatory submissions for drugs, biologics, and medical devices.
- Managing product registrations and regulatory documentation.
- Supporting Regulatory Product Life Cycle Management activities.
- Performing change assessments and regulatory impact evaluations.
- Working with TrackWise 8 for change control management.
- Using Veeva Vault RIMS for regulatory submissions.
- Tracking regulatory filings and submission status.
- Maintaining regulatory databases, trackers, and documentation.
- Collaborating with R&D, Manufacturing, and Quality Assurance teams.
- Ensuring regulatory compliance throughout the product lifecycle.
Candidates should possess:
- Bachelor’s Degree in B.Tech.
- 0–2 years of relevant experience.
- Strong understanding of:
- ISO 13485
- ISO 14971
- IEC 62304
- Excellent analytical and problem-solving abilities.
- Strong communication and teamwork skills.
- Good knowledge of:
- Microsoft Excel
- Microsoft Word
- Databases
- Ability to work independently and manage multiple priorities.
Ideal candidates should have knowledge of:
- Global Regulatory Affairs
- Regulatory Submission Preparation
- Medical Device Regulations
- Product Registration
- Regulatory Documentation
- Change Control Management
- TrackWise 8
- Veeva Vault RIMS
- Product Lifecycle Management
- Regulatory Compliance
- Cross-functional Collaboration
Based on similar entry-level Regulatory Affairs positions in Bangalore, the expected salary is:
₹6,50,000 – ₹9,00,000 per annum (Estimated CTC)
Actual compensation will depend on experience, qualifications, and Baxter’s compensation structure.
Working at Baxter offers several advantages:
- Global healthcare organization
- Opportunity to work on international regulatory submissions
- Exposure to drugs, biologics, and medical devices
- Career growth in Global Regulatory Affairs
- Collaborative work environment
- Learning opportunities with international teams
- Competitive compensation and employee benefits
This opportunity is suitable for:
- Fresh B.Tech graduates
- Candidates with up to 2 years of Regulatory Affairs experience
- Professionals interested in Medical Device Regulatory Affairs
- Candidates seeking Global Regulatory Affairs careers
- Engineers interested in healthcare and regulatory compliance
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