Greetings from People First Consultants
Hiring for a Regulatory Affairs Specialist with a leading medical device manufacturing company!
Experience: 2-6 years
Notice Period: Immediate - 1 month preferred
Location: Bangalore
Industry: Medical device manufacturing
We are looking for a detail-oriented Regulatory Affairs Specialist with hands-on experience in regulatory documentation and submissions for Class IIb medical devices.
You will ensure compliance with CE (EU MDR), USFDA, ISO 13485, and CDSCO MDR-17 standards.
If you are open to exploring new opportunities,
Kindly share your updated resume at hidden_email / WhatsApp at hidden_mobile
Looking forward to your response.
Best regards,
Vijayalakshmi
People First Consultants

Keyskills: regulatory medical equipment mdr regulatory affairs usfda medical devices
About People First (Hiring for client of People First)People First is a niche talent sourcing and learning and development consulting firm in service since 1995. Our vision is to evolve and inspire evolution in organizations and institutions to journey to their ‘next orbit’ in t...