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9 candidates for "Regulatory Affairs (RA)"
Seasoned professional specializing in Medical Device Regulation (MDR) remediation and ISO 13485–aligned Quality Management Systems (QMS). Experienced in compliance, audits, and continuous improvement to enhance…
Experienced Regulatory Specialist with a proven track record in the pharmaceutical industry. Skilled in Regulatory Affairs and Pharmacy, with a strong academic foundation from Mumbai…
Medical Electronics background from Dr. Ambedkar Institute of Technology Works at Tata Elxsi in regulatory affairs (APAC region) Prepares Global Submission Summary Documents (GSSD) &…
Regulatory Affairs Executive - QMS || ISO 13485 || Technical Document preparation|| GSPR || 510k USFDA Medical Device || EU MDR ||SFDA (GHAD )& CDSCO…
Senior engineer | Regulatory Affairs | EU MDR 2017/745 | ISO 13485 | ISO 14971 l Loftware | DHF remediation | Labeling | Kallick |…
Regulatory Engineer - Medical Device | DHF | ISO13485 | ISO14971 | Remediation | TrackWise | Change Control | MQMS | Medical Device Regulatory| 510k…