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Job Description
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
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,
Looking to get Placed? Try our Placement Guarantee Plan
Kindly share your updated resume athidden_email / WhatsApp at hidden_mobile
Looking forward to your response.
Best regards,
Vijayalakshmi
People First Consultants
Skills
Medical EquipmentRegulatory AffairsRegulatoryMedical DevicesMdrUsfdaIf an employer asks you to pay any kind of fee, please notify us immediately. Jobaaj does not charge any fee from the applicants and we do not allow other companies also to do so.
Important dates & deadlines?
Application Deadline
27 Oct 25, 01:49 PM IST
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