Zentiva, A Sanofi Company Work Values

Daily Duties at Zentiva, A Sanofi Company:

My primary responsibilities at Zentiva included - but were not limited to - continuous management of product information and package inserts of multiple marketed medicines throughout the product’s life-cycle. Project management of products during the whole regulatory process leading to a new registration. Providing timely notice to all concerned local affiliates about upcoming changes, variations and new registrations. Active participation at project meetings for products at various stages of development. My other duties comprised of contracting and overseeing preparation of so-called Readability/User Tests, and creating Bridging Reports where necessary. Majority of the materials was prepared in English and in accordance with the current EU drug regulatory legislation. I left Zentiva only due to family relocation to the US.

What they like about Zentiva, A Sanofi Company:

You give high priority to hiring firms with prestige. Market reputation and prestige of a firm may be determined through on-line research, and conversations with individuals working in your target industry. Note that firms "in the public eye" receive a great deal more critical publicity and attention than those operating with more anonymity. So as you assess your employment opportunities, be sure to seek out the positive aspects of the firm's reputation in addition to noting negative publicity the company may have received.

Tags

Immunology, Regulatory, Project management, Pharmaceuticals, Biotech, Clinical research, Drug development, Vaccines, Medical writing

Skills

Independent problem solving and strong organizational skills, Working knowledge of EU drug legislation, Clinical trails, Good Clinical Practice and FDA requirements, Knowledge of electronic documents management, Working experience with MedDRA system, Understanding of immunology, cell biology, antibody biology and molecular mechanisms of drug action, Practical and theoretical knowledge of molecular biology-related experimental techniques and flow cytometry, Medical writing with strong emphasis on detail in the pharmaceutical industry setting, Practice in writing project reports, grant applications and manuscripts for publication, Comfortable working in international teams., Project mamagement, Familiar with the research and regulatory life-cycle of medicines., Practical experience in preparation and delivery of oral presentations., Producing projects with Photoshop, Microsoft Office, and SharePoint, Employee training, Department planning and ability to set and keep deadlines, Drive to start and lead new projects with enthusiasm and persistence with focus on the ultimate goal, Equipped with critical thinking well applicable to any evidence-based discipline

These are some of the questions we asked our climbers about their experiences with Zentiva, A Sanofi Company: