от компании (организации): Abbott Laboratories в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Медицинское оборудование"
с заработной платой: по договоренности
Вакансия № 20138643 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Среда, 11 сентября 2024 года.
Дата обновления вакансии № 20138643 на сайте Работа в Москве и Московской области (МО, Подмосковье): Понедельник, 23 сентября 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 20138643 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 (Abbott Diagnostics)
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 now looking for Regulatory Affairs Specialist to strengthen our Regulatory Affairs Team in Laboratory Diagnostics.
Main responsibilities:
- Responsibility for insuring earliest possible registration of all new or in-line products, claims, formulations and/or strengths, along with price registration/re-registration, shelf-life changes according to adopted registration strategies (and company's high ethical standards policy).
- Reviewing registration files and all related documentation of the Company's products and preparing such documentation in line with local normative regulations.
- Preparing Application Forms and other documentation for filing and registration of new products. Ensuring that all documentation, samples, commercial packs and other items are provided to relevant agencies as needed.
- Establishing and maintaining good working relationships with all involved regulatory and other institutions. Keeping track of new normative documents related to registration of medicines.
- Cultivating best possible relations with local regulatory bodies and opinion leaders and enhancing the Company's image in the medical community in general.
- Handling all issues related to changes in the Company's products status and performing regulatory related surveys in the country.
- Preparing and reviewing package labels and inserts for Company's respective new and in-line products registered in the country.
Requirements:
- Higher education.
- At least 2 years of experience in Regulatory Affairs (medical equipment or medical devices).
- Strong willing to develop in IVD regulatory affairs field.
- Intermediate English.
- Excellent 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.
*Заявленное описание вакансии, а также список требований к вакансии не является полным.
Откликнуться на эту вакансию: Regulatory Affairs Specialist (Abbott Diagnostics)
Предыдущая вакансия:
Вакансия № 20138638 на должность Главный бухгалтер от компании ООО Авиа Кейтеринг в городе (населенном пункте) Домодедово