Registration specialist (contract duration 1 year)

WHY SERVIER?

Servier is the 2nd largest pharmaceutical Group in France and 34th largest pharmaceutical Group worldwide. Our status of an independent company assures our stability. Servier maintains the highest ethical standards for our work and business management. The company offers wide opportunities to learn and develop, within a friendly team committed to drive global changes in healthcare. In April 2021, according to the results of the international HR certification program "Best Places to Work" Servier Ukraine was recognized as one of the best places to work in Ukraine.

JOINS US!

 Learn more about Servier: https://rabota.ua/company701738

 We are looking for a REGISTRATION SPECIALIST to join our Regulatory Department team in Kyiv

MAIN REQUIREMENTS: 

• University Degree in medicine or pharmacy;
• 2-3  years of related experience ;
• Profound knowledge of Ukrainian legislation/guidelines pertaining to Marketing Authorization of medicinal products and maintenance of product during its lifecycle;
• Proven knowledge of Regulatory Affairs procedures for Marketing Authorization/renewal/variations;
• Good knowledge of English (at least Intermediate level);
• Excellent knowledge of the Ukrainian language (both oral and written);
• Good communication and writing skills;
• Good organization and planning skills with strong attention to details, deadlines and ability to multitask;
• Ability to demonstrate effective time-management skills by prioritizing workload.

 WE SUGGEST:

 One of the best social packages in the industry: official full-time employment, 28 days of yearly vacation, Life and Medical insurance;

• Compensation of lunches;
• Competitive salary;
• Work with original high-quality medicines on an ethical basis.

RESPONSIBILITIES:

• Effective planning and processes development of the registration procedures (registration, renewal, variations) for company products;
• Responsible for products packaging compliance review with further validation for production and submission of the mock-ups to the Regulatory Authorities;
• Planning, preparation and conduction of the GMP recognition of Company’s manufacturing sites in Ukraine;
• Maintenance of the Company’s Regulatory databases;
• Timely sharing info with concerned departments, effective communication, participation in cross-functional projects
• Thorough fulfillment of working responsibilities in due time.

 If you feel like joining our team, send your CV in English to Отправить резюме