Sr. Executive - Regulatory (Gujarat)
Job Description
Preparation, coordination and compilation of regulatory DOCUMENTATION and dossiers for Medical Device registrations worldwide.
Liaise with Notified Bodies and Regulatory Authorities during Medical Device registration procedures and during lifecycle Participation in audits by a Notified Body or Agencies Maintenance of Medical Device registrations in accordance to new regulatory and technical requirements and as required from technical and labeling changes
Close monitoring of regulatory requirements issued by the authorities and evaluation of their relevance for the registration status of our products Regulatory support to the technical departments as well as to QA functions and manufacturing departments during development and lifecycle of Medical Devices Support the generation and maintenance of design history files
Requirements
Current Industry – Pharma / Biotech
Qualification – B.Sc. / M.Sc. / B.Pharm / M.Pharm
Functional Area – Quality (QA-QC)
Total Experience 2 Yrs to 4 Yrs in QA / QC in Pharma Industry
Company Description
Frisch Medical is the change
in medical device industry, forthcoming with… innovation and invention. We dwell in cardiac division & Our product
portfolio includes all cardiac appliances with the innovative specifications. Read full description
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