Medical Device Regulatory
Shinelife Group · Mumbai · onsite · Posted 37d ago
₹3.0L - ₹3.6L PA2–3 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
- Strong knowledge of CDSCO, SUGAM, Medical Device Rules 2017, ISO 13485, Good Documentation Practice. Ensure compliance with ISO 13485 & QMS requirements
- Return Filing, EPR - E waste & E Plastics
- Making SOP's as per standard
- Supporting in Audits
Perks and benefits
Provident fundSourced from naukri
Skills
CDSCO and BIS DocumentationMaking SOPs of the Equipment as per StandardsISO AuditISO Documentation