Reporting to: Assistant Manager – Regulatory Affairs Division: Ortho Implants Location: Chennai No. of Positions: 1 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.
Full-time
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