Website TTK HEALTHCARE
Post Name: Regulatory Affairs (Medical Devices)
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.
Knowledge of any other document/image editing software is a plus.
Possesses logical, analytical and verbal skills.
