от компании (организации): Abbott Laboratories в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Медицинское оборудование"
с заработной платой: по договоренности
Вакансия № 10941537 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Воскресенье, 1 сентября 2024 года.
Дата обновления вакансии № 10941537 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 № 10941537 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 (Diagnostics)
Main responsibilities:
- Responsibility for developing a comprehensive registration strategy in close cooperation with the personnel dealing with sales, operations, vaccines and marketing, taking into consideration Company's interests and normative requirements.
- 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 normatine 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, pharmaceuticals, chemical products)
- Strong willing to develop in IVD regulatory affairs field;
- English – written, spoken
- Excelent 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
Benefits:
- Medical insurance for the employee and his children (100% coverage);
- Medical insurance for a spouse (50% coverage);
- Life insurance (accidents)
- Food allowances
- Various training programs
- Employee assistance programs
- Compensation costs for fitness (for employees who have been with the company for over 1 year)
Откликнуться на эту вакансию: Regulatory Affairs Specialist (Diagnostics)
Предыдущая вакансия:
Вакансия № 10941533 на должность Менеджер отдела продаж от компании Медстал в городе (населенном пункте) Москва