Обязанности:
Our client is an international company who are looking for a Goods Registration Specialist to join their team. Responsibilities: Communicates by e-mail, telephone, and in person with product consultants, manufacturers, and other departments on a daily basis. Сontact with a third parties/ authorities to submit technical and non-technical data from manufacturers and various company sources. Develops new and revised printed components through defined workflows in the company database, ensuring their regulatory acceptability prior to printing. Maintains and renews existing certificates. In a timely fashion, communicates to direct supervisors all regulatory developments presented by consultants and importers. Communicates to direct supervisor any potential organizational or procedural changes that could improve efficiencies within and outside of the Specialist role. Carries out all responsibilities in an honest, ethical and professional manner. Requirements: Minimum 1 year industry or related work experience (Regulatory area) Ability to systematically analyze problems and propose thorough, efficient and creative solutions Regulatory knowledge in Food, Food supplements and other related products Fluent English Conditions: Competitive salary Benefits package Hybrid work schedule.Специалист по регистрации медицинских изделий / Regulatory affairs specialist (Medical devices)
Договорная
Москва
Manpower
Специалист по регистрации медицинских изделий / Regulatory affairs specialist (In Vitro)
Договорная
Москва
MINDRAY MEDICAL RUSSIA , LTD
Regulatory Affairs Assistant / Ассистент Отдела регистрации
Договорная
Москва
Johnson & Johnson Consumer Health