Interesting position as Regulatory Affairs Associate Animal Health
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Biotechnology organization, based in Antwerpen Belgium.
An interesting company who is dedicated to Animal Health improvement. The company is an growing family company, and therefore looking for somebody to strengthen the RA team. The client has another site in Europe and is active in 100+ other countries worldwide (Europe, Middle East, South East Asia, Africa and South and Central America) through a network of exclusive distributors.
ROLE DESCRIPTION
In this role you will be responsible in the process of research, development, registration, production and marketing of veterinary medicines. You'll work within a dynamic team where you will learn and grow in a career of obtaining and maintaining world-wide marketing authorisations of veterinary medicines.
RESPONSIBILITIES
- Preparing, writing and updating regulatory submissions of new and old veterinary medicinal products (both generic and non-generic)
- Identifying regulatory priorities and preparing quality documentation accordingly, as needed for variations and dossier compliance
- Maintaining regular contact with other departments
- Develop and maintain local and international regulatory expertise (pre- and post-authorisation)
REQUIREMENTS
- Scientific Master degree (a degree in Pharmacy is an asset)
- Experience in regulatory aspects in the area of (veterinary) medicinal products.
- Proactive approach, work independently
- Be able to meet deadlines and thus working under pressure
- Proficient in English and French
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
