от компании (организации): Abbott Laboratories в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Фармацевт"
с заработной платой: по договоренности
Вакансия № 23382133 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Вторник, 3 сентября 2024 года.
Дата обновления вакансии № 23382133 на сайте Работа в Москве и Московской области (МО, Подмосковье): Воскресенье, 22 сентября 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 23382133 может быть уже занята. Администрация сайта Работа в Москве и Московской области (МО, Подмосковье) приносит извинения за доставленные неудобства.
Требования к опыту работы:
1–3 года
Тип занятости:
полная занятость
График работы:
полный день
Дополнительные сведения о вакансии: Regulatory Affairs Specialist
For 130 years Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, minimally invasive medical devices, coronary stents, nutritionals and branded generic medicines. We help people with diabetes effectively manage it without painful finger pricks.
Abbott is one of the most diversified companies in healthcare. Our 109,000 colleagues serve people in more than 160 countries.
We are looking for Regulatory Affairs Specialist to join Abbott Rapid Diagnostics (Infectious Disease) Division. Outsourcing (Ancor)
Main responsibilities:
- Managing full registration of all products in collaboration with manufacturer and with/without local vendor for registration according to the Global Submission Process and all local requirements;
- Registration dossier preparation in accordance with the local requirements (documents creation, interaction with the manufacturer, consulting and translating agencies);
- Maintain the local technical, toxicological, clinical evaluation (including design development, coordination, report validation etc.);
- Establishing and maintaining good working relationships with all involved regulatory and other institutions;
- Identify new regulations or updates of existing regulation in the Russian Federation, EEU;
- Maintain a product re-registration due changes on manufacturing site according to adopted registration strategies (and company's high ethical standards policy);
- Responsible for in time vigilance reporting according local legislation;
- Obtaining other required documents (declarations of conformity, import permits, licenses etc.);
- Supporting local team on regulatory issues.
Requirements:
- Higher education (pharmacy, biology, chemistry, medicine, engineering, quality, law etc.);
- At least 1 years of experience in Regulatory Affairs (medical equipment - preferably, pharmaceuticals, chemical products);
- Good knowledge of Russian Medical Devices regulations;
- English - Upper Intermediate;
- Knowledge of MS Office (Word, Excel);
- Personality: team player, well organized, attentive to details, enthusiastic, quick learner;
- Ability to work with big amount of information.
Outstaffing contract with Ancor.
Откликнуться на эту вакансию: Regulatory Affairs Specialist
Предыдущая вакансия:
Вакансия № 23382106 на должность Фармацевт-провизор (м. Рязанский пр.) от компании МАГНИТ, Розничная сеть в городе (населенном пункте) Москва