OPENING FOR A WELL KNOWN TIC COMPANY In INDIA

Minimum Requirements:

must have 10 years of professional experience in the medical device industry with at least 4 years in the design, manufacturing, testing.

Roles & Responsibilities

• Auditing Quality Management Systems (mainly ISO 13485).
• Checking compliance with regulations (e.g., EU MDR, FDA 21 CFR 820, MDSAP).
• Assessing technical documentation, validation, and product safety evidence.
• Experience with Risk Management EN ISO 14971;
• Qualified MDR Assessor from a reputed EU Notified Body, desirable

**Interested Candidates Can Apply Or Share Your Updated CV on [email protected]**