Intervet International in Boxmeer (NL) is specialised in the development, production and sale of animal-medicine. With a turnover of € 1,125 million in 2006, Intervet rose to third place for veterinary products on the World market. Intervet is market leader in the Netherlands. At this moment, the Intervet Group has more than 50 branches worldwide, and provides work for 5300 employees. In the U.S., more than 950 employees are active, of which more than 250 in Research and Development. Due to a recent take-over, Intervet is now a facet of the Schering-Plough organisation.

International Regulatory Affairs Biologicals

The Regulatory Affairs Department is a dynamic internationally orientated environment in which a team of dedicated specialists is responsible for the world-wide registration of the Intervet biologicals range. The department is a key factor in the success of Intervet International and forms the bridge between the Intervet R & D organization and the Regulatory Authorities in more than 120 countries. Its activities include the compilation of high-quality scientific dossiers for their products, co-ordination and support of the registration procedures and co-ordination of international field trials. The department is embedded in the international R & D organization and consists of cross-linked teams responsible for viral, bacterial and parasitological vaccines, international clinical trials, export services and regulatory policy.
 
Vacancy: Scientific Editor Vaccines.
Your position

Within the multi-disciplinary team of scientific editors vaccine, you will be responsible for the preparation of high-quality scientific dossiers for new or existing vaccines. You will also be responsible for the follow-up of records, which have been submitted to competent authorities and provide answers to any questions asked. You will be a member of R & D project teams to advise regarding the appropriate set of data required for international licensing or renewal. Co-ordination of regulatory issues involved in product transfers may also be part of your activities. Depending on the specific profile of the candidate, the focus of the position may vary.
 
Your Profile

The ideal candidate would have at least a master's degree in one of the biomedical sciences (eg, virology, molecular biology) or veterinary sciences and have experience in vaccine research, vaccine production or quality control. A few years experience in the human or veterinary biological pharmaceutical industry and / or a regulatory agency would be an asset. Your English is fluent in speech and writing, preferably while you speak French and German. You have excellent communication skills and can cope with temporary stress. Intervet strongly believes in the value of an informal, non-hierarchical working environment where initiative is stimulated and teamwork is valued. If you feel comfortable to work under such conditions you are invited to respond.
 
Remuneration package

Intervet offers you a challenging position within an organization where growth and a dynamic working environment are key concepts. You will enjoy good career prospects, an excellent salary and other benefits.
 
For information about this vacancy please contact:
Jeffrey R. Hensen, Sr.. Consultant
Phone: + 31 (0) 6-53 17 89 48
E-mail: hensen@themagroup.nl