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Halma plc, a FTSE 100 global group of life-saving technology companies, is hiring a Regulatory Affairs Executive in Bengaluru, Karnataka, India. This is a full-time, on-site role for candidates with 1–3 years of regulatory affairs experience in India MDR (Medical Device Rules).
If you are passionate about regulatory compliance, medical devices, and want to grow with a company that values innovation, diversity, and sustainability, this opportunity is for you.
Key Responsibilities
- Conduct regular meetings with international regulatory teams to address evolving India market needs.
- Assist global teams in understanding India MDR with clarity.
- Act as a consultant and advisor for Indian regulatory requirements.
- Liaise with CDSCO officials in Delhi and external India MDR consultants as needed.
- Manage regulatory licenses through platforms and ensure compliance across Halma group companies.
- Handle PESO license applications, GEM portal registrations, and documentation.
- Monitor regulatory changes to minimize business disruption.
- Represent Halma in advocacy through MTAI membership.
- Ensure executional rigor and due diligence in all licensing requirements.
Qualifications & Experience
- Degree in Regulatory Management (or related field).
- 1–3 years of hands-on experience in India MDR licensing.
- Strong knowledge of legal metrology, labeling, UDI, pricing, customs, and trade margin regulations.
- Experience with regulatory license platforms.
- Exposure to European MDR and FDA regulations will be an advantage.
- Strong communication, stakeholder management, and process-orientation skills.
Why Join Halma plc?
- Work with a Great Place to Work® certified organization.
- Employee-centric culture with autonomy, respect, and team spirit.
- Safe and inclusive workplace valuing diversity and individuality.
- Opportunities for non-linear career growth and entrepreneurship.
- Be part of a global group operating in 23 countries with innovative technology-driven companies.
How to Apply
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