от компании (организации): ООО Алкон Фармацевтика в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Сертификация"
с заработной платой: по договоренности
Вакансия № 21859280 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Суббота, 14 сентября 2024 года.
Дата обновления вакансии № 21859280 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 № 21859280 может быть уже занята. Администрация сайта Работа в Москве и Московской области (МО, Подмосковье) приносит извинения за доставленные неудобства.
Требования к опыту работы:
не требуется
Тип занятости:
полная занятость
График работы:
полный день
Дополнительные сведения о вакансии: Regulatory Affairs Specialist
About us
Alcon is the global leader in eye care, dedicated to helping people see brilliantly. With our 70-plus-year heritage, we are the largest eye care device company in the world – with complementary businesses in Surgical and Vision Care. Being a truly global company, we work in over 70 countries and serve patients in more than 140 countries. We have a long history of industry firsts, and each year we commit a substantial amount in Research and Development to meet customer needs and patient demands.
Currently we are looking for a Regulatory Affairs Specialist.
Join Alcon and help the world See Brilliantly!
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;
- 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.
Background and experiences
- Higher education;
- At least 2 years of experience in Regulatory Affairs (medical equipment or medical devices);
- Awareness of the requirements of relevant local and international regulations;
- Ability to work with big amount of information;
- Personality: team player, well organized, attentive to details, enthusiastic, quick learner;
- English - Upper Intermediate.
We offer
- Opportunity to work on best in class technology platforms and solutions, having the broad view at the technologies & tools used in Alcon globally;
- Opportunity to work in a high paced agile environment with people who are passionate of delivering outcomes and a culture of simplification and ownership;
- Empowerment to create, improve and work on the innovative solutions that will deliver the highest value and determine the direction of our organization growing & developing;
- Attractive compensation and benefits package: life, accident & medical insurance, meal allowance, mobile allowance;
- Brand new office with a lot of facilities inside, located at Sokol
Откликнуться на эту вакансию: Regulatory Affairs Specialist
Предыдущая вакансия:
Вакансия № 21859269 на должность Regulatory Affairs Specialist (Established Pharmaceuticals Division) от компании Abbott Laboratories в городе (населенном пункте) Москва