Job Description
Prepare and review Clinical Evaluation Reports (CERs) for medical devices.
Conduct systematic literature searches using relevant databases and methodologies.
Perform State of the Art (SOTA) assessment and clinical data analysis.
Support clinical evaluation, PMS, PMCF, and regulatory documentation.
Ensure documentation aligns with applicable medical device regulatory requirements.
Apply robust technical writing, analytical, and documentation skills to prepare high-quality reports.
Medical device industry experience with exposure to clinical/regulatory affairs is preferred.
📌 Qa Ra Specialist Noida
🏢 Saraca Solutions
📍 Noida
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