Role & responsibilities
Key Responsibilities:
Assist with Clinical Evaluation Reports (CERs), literature reviews, clinical evidence, and performance data documentation.
Support CDSCO submissions, technical files, clinical evaluation records, and post-market surveillance documentation.
Support ISO 10993 biological evaluation plans/reports, testing coordination, and follow-up with testing laboratories.
Key Requirements:
Solid research, documentation, and analytical skills.
Positive proficiency in MS Office.
Exposure to clinical evaluation, regulatory documentation, or medical device documentation will be an added advantage.
📌 Clinical Specialist Gujarat
🏢 Meril
📍 Gujarat