от компании (организации): GE (General Electric Company) в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Лекарственные препараты"
с заработной платой: по договоренности
Вакансия № 15988440 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Пятница, 26 июля 2024 года.
Дата обновления вакансии № 15988440 на сайте Работа в Москве и Московской области (МО, Подмосковье): Вторник, 24 сентября 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 15988440 может быть уже занята. Администрация сайта Работа в Москве и Московской области (МО, Подмосковье) приносит извинения за доставленные неудобства.
Требования к опыту работы:
3–6 лет
Тип занятости:
полная занятость
График работы:
полный день
Дополнительные сведения о вакансии: Regulatory Affairs Specialist, Contrast Media (GE Healthcare)
About GE
GE Healthcare is a leading global medical technology and digital solutions innovator, GE Healthcare enables clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications and services, supported by its Edison intelligence platform. With over 100 years of healthcare industry experience and around 50,000 employees globally, the company operates at the center of an ecosystem working toward precision health, digitizing healthcare, helping drive productivity and improve outcomes for patients, providers, health systems and researchers around the world. Follow us on Facebook, LinkedIn, Twitter and Insights , or visit our website for more information.
Role Summary/Purpose
Regulatory Affairs Specialist works with a team of Regulatory Affairs experts to prepare high quality documentation for registration. Regulatory Affairs Specialist will be expected to interact with all functions within GE Healthcare medical diagnostics and interact with external contacts as necessary including maintenance and tactical level communications with Regulatory Authorities.
Essential Responsibilities
- Ensuring accuracy, scientific validity and optimal presentation of submission documents that meet current best practice standards;
- Effectively planning submissions and regulatory documents to agreed timelines and ensuring alignment with agreed strategy;
- Providing regulatory advice to teams on assigned projects;
- Identifying regulatory issues and resolving them with relevant departments or country offices;
- Communicating with Regulatory Authorities and contractors to expedite review and approval of submissions;
- Safekeeping of documents archive in coherent order;
- Ensuring compliance of label creation process (AMS) with local regulations.
Qualifications/Requirements
- Bachelor’s Degree in a related field such as: Regulatory Science, Biomedical Engineering, Biology, Chemistry, Pharmaceutical Science, Pharmacy;
- Ability to prioritize, plan & evaluate deliverables;
- Knowledge & experience conducting scientific, regulatory, legal, or business research;
- Excellent verbal and written communication and presentation skills with the ability to communicate in English in an easy to understand manner;
- Ability to independently resolve straightforward issues and identify proposed strategy for complex issues;
- Demonstrate good interpersonal skills required to build relationships with and influence internal departments, country offices and externally with Regulatory Authorities.
Откликнуться на эту вакансию: Regulatory Affairs Specialist, Contrast Media (GE Healthcare)
Предыдущая вакансия:
Вакансия № 15988433 на должность Аналитик в отдел управления ликвидностью от компании Центральный банк Российской Федерации в городе (населенном пункте) Москва