Job highlights
Education: BE/ B Tech in Biomedical Engineering / M Pharm Regulatory Affairs .
Proficiency in English,Proof reading skills and MS Office skills mandatory
Experience: 2 - 4 years Exp
Experience in scientific writing / clinical documentation role

Education: B.E/ B. Tech in Biomedical Engineering / M.

Pharm Regulatory

Affairs

Experience: 2 - 4 years Exp. in scientific writing / clinical documentation role preferred

KEY RESPONSIBILITIES
Technical writing, literature search, review, data extraction, Data Analysis and appraisal as per guidelines for medical devices (Class III)
Scientific development and template preparation for protocols and procedures, related to ortho implant surgeries during piloting phase as well post-marketing surveillance studies.

DESIRED CANDIDATE PROFILE
Experience in scientific writing/clinical documentation role.
Exposure to medical device regulatory affairs, is preferable.
Proficiency in English, Proof reading skills and MS Office skills mandatory.
Knowledge of any other document/image editing software is a plus.
Possesses logical, analytical and verbal skills.

📌 Executive Regulatory Affairs Medical Devices Chennai
🏢 TTK Healthcare
📍 Chennai