Regulatory Specialist (veterinary direction)

Вакансия № 2350623 от компании AVICONN на Электронной Службе Занятости Населения Москвы.

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☑ Основной блок:

Опыт работы: 3–6 лет.

Тип занятости: полная занятость.

График работы: полный день.

Зарплата: по результату собеседования.

Примерное место работы: Россия, Москва.

☑ Актуальность объявления:

Это объявление № 2350623 добавлено в базу данных: Среда, 19 февраля 2025 года.

Дата его обновления на этом интернет-ресурсе: Воскресенье, 16 марта 2025 года.

☑ Статистика предложения работы № 2350623:

Прочитано соискателями - 153 раз(а);
Отправлено откликов - 0 раз(а);

☑ Репутация компании "AVICONN":

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☑ Подробности о вакантном месте:

Position Description:
Responsible for maintain life cycle of existing product registrations and ensure in-time submission and approval of new products registrations and renewals. Has to ensure 100 % compliance of product registrations and packaging materials with regulations of local legislation.

Functions, Duties, Task:

To review and assess regulatory documentation prepared by global regulatory department for further submissions to local Regulatory Authorities;
Own interactions with Competent Authorities at all steps of product registration process , prepare dossier documents, arrange translation, complete registration dossiers for new products submissions in accordance with yearly registration plan , to ensure in-time receiving of approval documents;
To accomplish and ensure in-time submissions and approval of renewals and variations;
To arrange payment of local regulatory fees, to ensure import permits obtaining for registrations samples delivery;
To identify potential risks and gaps in the assigned projects and propose solutions to mitigate those;
Accountable for providing the most accurate and up-dated information about regulatory requirements in geography of responsibility in respond to any intra-company internal request
Deliver projects in time, whilst ensuring communication of status and requirements across multiple business functions, organize and hold regular calls and F2F meetings with involved function areas;
Ensure regulatory compliance of printed packaging materials
Prepare responses to official requests received from the Local Regulatory authorities;
To review and ensure compliance of local promotional materials;
Understand and act according to regulatory compliance and local policies, track and follow-up on any changes in regulatory requirements of CIS/RU
Ensure compliance with procedures and systems necessary to maintain proper regulatory records
Support other departments with RA information/communication

Minimum Qualification (education, experience and/or training, required certifications):

University degree in pharmaceutical or medical sciences, with veterinary study preferred
English language - advanced written, fluent speaker
Good knowledge and understanding of local legislation in regulatory sphere
Experience of working in Regulatory Affairs in local either international company

Additional Preferences:

Positive attitude and fit with Elanco cultural pillars
Demonstrated experience in working effectively with teams and various functional areas
Accuracy and analytics mindset
Excellent organizational and implementation skills
Personal accountability and strong drive for execution
Ability to set priorities and manage multiple tasks.

Conditions: