10/03/2020
Job Description : To deal with all technical operational matters ( i.e. Application and Contract Review, TCF / Medical Device File Review, On-site Assessments / Audits) related to ISO 9001, ISO 13485, MDR 2017 Approval, CE Mark Certification (Medical Devices and In-Vitro Diagnostic Medical Devices ) with present and potential clients. The scope is from Application stage to Audit and Certification stage including post certification services i.e. surveillance activities including surveillance audits
