Executive Regulatory Affairs (medical Devices) Job in Ttk Limited

Executive Regulatory Affairs (medical Devices)

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Job Summary
  • 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.
Experience Required :

2 to 4 Years

Vacancy :

2 - 4 Hires

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