"Executive – Regulatory Affairs Job in Bengaluru | Global Healthcare Company Hiring"
 |
(Career Opportunity: Executive) |
Introduction
Pharmaceutical and medical device regulatory professionals are currently witnessing strong demand across India, especially in metro cities like Bengaluru. With the rapid growth of medical device regulations under India MDR, global healthcare companies are actively hiring skilled regulatory experts.
A leading global healthcare and technology-driven organisation has announced an excellent career opportunity for the position of Executive – Regulatory Affairs in Bengaluru, India. This role is ideal for professionals who already have hands-on exposure to India Medical Device Rules (MDR) and want to build a long-term career in regulatory compliance, licensing, and international coordination.
If you have 1–3 years of regulatory affairs experience, this position can be a strong stepping stone toward global regulatory roles.
About the Company
The hiring organisation is a globally established healthcare and medical technology company operating across multiple international markets. The company is known for delivering innovative healthcare solutions while strictly adhering to global regulatory and compliance standards.
-
Industry: Healthcare & Medical Technology
-
Global Presence: Multiple countries
-
Headquarters: International (Global Operations)
-
Established: Early 2000s
-
Employees: Thousands worldwide
-
Focus Areas: Medical devices, healthcare technology, regulatory compliance, and patient safety
The company works closely with international regulatory authorities and industry bodies to ensure compliance with evolving healthcare regulations, making it an excellent workplace for regulatory professionals.
Job Overview Summary
The Executive – Regulatory Affairs role focuses on managing and supporting regulatory activities related to India MDR and medical device compliance. The selected candidate will work closely with international regulatory teams, Indian regulatory authorities, and consultants to ensure smooth licensing, approvals, and ongoing compliance.
This role combines technical regulatory knowledge, stakeholder communication, and regulatory technology management, offering exposure to both Indian and global regulatory frameworks.
Vacancy Details (Official)
-
Job Title: Executive – Regulatory Affairs
-
Location: Bengaluru, India
-
Experience Required: 1–3 Years
-
Qualification: Degree in Regulatory Management or equivalent
-
Industry: Healthcare / Medical Devices
-
Job Type: Full-Time
Roles & Responsibilities
As an Executive – Regulatory Affairs, the selected candidate will:
-
Coordinate regularly with international regulatory teams to align Indian market requirements
-
Provide expert guidance on the India Medical Device Rules (MDR)
-
Act as a regulatory consultant and compliance advisor within the organisation
-
Liaise directly with CDSCO authorities, including official meetings in Delhi
-
Collaborate with India MDR consultants when required
-
Support the implementation of regulatory technology platforms for license tracking and documentation
-
Ensure risk reduction and continuity of regulatory compliance
-
Represent the organisation through MTAI membership and advocacy activities
-
Manage PESO license applications and associated regulatory documentation
-
Handle GEM portal registration, audits, and submissions for overseas entities
This role demands precision, regulatory awareness, and proactive communication.
Eligibility Criteria (Official)
✔ Degree in Regulatory Management or equivalent qualification
✔ 1–3 years of experience in Regulatory Affairs
✔ Experience specifically related to India MDR regulations
✔ Exposure to end-to-end MDR licensing processes
Skills Required
-
Strong understanding of India MDR and CDSCO procedures
-
Knowledge of regulatory license management systems
-
Familiarity with legal metrology, labelling, UDI, MRP, pricing & trade margins
-
Awareness of customs and import regulations
-
Basic exposure to European MDR and US FDA regulations (preferred)
-
Excellent communication and coordination skills
-
Strong compliance mindset with attention to detail
-
Ability to work with internal teams, consultants, and regulators
Salary Estimate
Estimated Salary Range:
₹6 LPA – ₹10 LPA (depending on experience, skills, and regulatory exposure)
Note: Actual salary will be decided by the company during the interview process.
Interview Details (Official)
Required Documents
Candidates should keep the following documents ready:
-
Updated Resume / CV
-
Educational certificates
-
Experience certificates (if applicable)
-
Government ID proof
-
Regulatory training or certification documents
-
Passport (if required for global coordination)
How to Apply
Interested candidates can apply directly through the official career portal of the company.
👉 Apply for Executive – Regulatory Affairs (Bengaluru)
(Apply online only. No walk-in or email application mentioned.)
Frequently Asked Questions (FAQs)
Q1. Is this job suitable for freshers?
❌ No, minimum 1 year of Regulatory Affairs experience is required.
Q2. Is India MDR experience mandatory?
✅ Yes, hands-on India MDR exposure is essential.
Q3. Will there be travel involved?
✅ Yes, occasional travel to Delhi for CDSCO meetings may be required.
Q4. Is knowledge of FDA or EU MDR compulsory?
❌ Not compulsory, but it is an added advantage.
Q5. Is this a permanent role?
✅ Yes, it is a full-time permanent position.
Final Conclusion
The Executive – Regulatory Affairs Job in Bengaluru is an excellent opportunity for pharma and medical device professionals looking to strengthen their regulatory career in a global healthcare environment. With exposure to India MDR, CDSCO, PESO licensing, and international regulatory coordination, this role offers both professional growth and global compliance experience.
If you are serious about building a future in regulatory affairs and medical device compliance, this opportunity should not be missed.
Apply now and take the next step toward a successful regulatory career.
⚠️ Disclaimer
This job information is collected from official company sources and public job listings. We do not charge any fee for job applications. Candidates are advised to verify details from the official company website before applying.
📄Resume Getting Rejected Again & Again?
👉 Not getting interview calls?
Most pharmaceutical job applications fail due to poorly formatted or non-ATS-friendly resumes.
👉 Get your Pharma Resume professionally written by experts:
✔ Fresher & Experienced
✔ ATS-friendly
✔ HR-approved format
🔗 Check Resume Writing Service:
https://www.pharmaduniya.com/p/professional-pharma-resume-writing.html
Share on WhatsApp
Explore More Verified Pharma Career Opportunities:
Stay updated with Pharma Duniya for daily verified jobs, internships, and career guidance.
.png)
