- 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
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.