S
Saraca Solutions
Qa Ra Specialist
Skills
Data Analysis
2 months ago
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Important information
Contract type:
Permanent
Location:
Chennai, Tamil Nadu, India
Work mode:
Onsite
Published on:
24 August 2026
What they need
- 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 strong technical writing, analytical, and documentationskills to prepare high-quality reports.
- Medical device industry experience with exposure to clinical/regulatory affairs is preferred.
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