Consultant (Scientific/ Technical - Non-Medical)

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About the Organization

The Indian Council of Medical Research (ICMR), New Delhi, is the apex body in India for the formulation, coordination and promotion of biomedical research. Established in 1911, it is one of the oldest medical research bodies in the world.

Education Qualification/Required Skills & Experience

• Professionals having proven competency and success in their area of specialization, with at least 10 years of postqualification experience and should possess minimum M.Sc. / B.Tech / BE / MCA / MPH / B. Pharm / BSMS / MD in AYUSH or equivalent qualifications with relevant experience in Manufacture/Testing/ Regulatory affairs of Medical Devices & Project Management with multi stakeholders collaboration in innovation management

                               OR

• Retired Government employees, with requisite qualification and who were in the regular Pay Level-10 and above and having at least 10 years’ experience in the required specialization.

Desirable Skills / Experience:

• Ability to communicate regulatory requirements and strategies effectively.
• Experience of handling data of Pre-Clinical/ clinical research studies.
• Experience in making SoPs/ Guidelines on Medical Device development/usage/ Regulations.
• Experience of handling regulatory matters & having knowledge of ISO 9001, ISO 13485, Medical Device Rules2017, ISO 14971, IEC 62304, internal audits, quality assurance, clinical evaluation/ performance evaluation, medical device design and development. Oversee end-to-end monitoring of the projects funded through handholding support of MedTech Mitra, facilitate technical & financial review.
• Coordinate activities among MedTech Mitra stakeholders and innovators.
• Develop and monitor project timelines, budgets disbursal and milestones.

For more information please check the Link

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