Regulatory Affairs Supervisor

Старший специалист по регистрации

№49137

Medical Equipment

Moscow, Russia

Regulation

Permanent

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Our client, international manufacturer of medical devices and equipment, opens the position of a Regulatory Affairs Supervisor

Responsibilities

- Develop and follow up assigned projects, prepare regulatory submissions necessary for new product, prepare additional data - Ensure compliance of the packaging and instruction for use of the products with European and national regulations - Interact with regulatory agencies, respond to their requests - Monitor legal and regulatory issues, new tendencies in the Russian regulations, Gather, communicate and recommend the regulatory changes - Provide risk assessments and regulatory options - Perform the complaint handling

Requirements

- Higher education in medical or pharmaceutical areas - 2 years + of experience in Regulatory Affairs (medical devices) - Written and spoken English - Quality audit experience is preferable

Note

Every day we receive a large number of responses, unfortunately, we are able to contact only the candidates whose profile best suits the requirements of the vacancy. Get the answer may, within two weeks. We wish you success in finding a new job!