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Sr. Executive RA

Exp. :: 3 - 8 years
Package :: 3-6 Lacs P.A.
Location :: Noida, Faridabad, Delhi / NCR

Job description

To lead, establish, maintain, and continually improve the Quality Management System (QMS) in accordance with ISO 13485:2016 and EUMDR. Preparation and maintenance of Technical Files of Medical Equipment as per MDR 2017/745, ISO 14971, ISO 10993-1.

To plan, establish, document, implement, maintain, and update a post-market surveillance. He shall ensure that the post-market surveillance obligations comply with Article 10(10) of the EU Regulation 2017/745 & other applicable standards.

Design & development documentation.
Role: Quality Consultant
Industry Type: Pharmaceutical & Life Sciences
Department: Quality Assurance
Employment Type: Full Time, Permanent
Role Category: Quality Assurance - Other

Education

UG: Any Graduate

Key Skills

European Union Medical Device Regulation, qa, Regulatory Affairs, RA