Regulatory Affairs Associates
Vacancy number 012/W
The position:
We are looking for co-workers for advisory and hands-on work in various fields of regulatory affairs. Based on your knowledge and experience you are very familiar with the regulatory field and know how to respond adequately and creatively to the many registration problems on the road to approval (FDA, EMEA). You assess and write registration documentation and give registration-strategic advice in (among other things) drug development routes, both independently and in team efforts. The work will be done both at the office and at our clients’ location. Our clients are demanding with regard to your level of knowledge, drive, communication and documentation skills and produced results.
Your profile:
You feel comfortable in a quality- and result-driven team. You have several years experience in regulatory affairs and writing and assessing (CTD) dossiers. You have obtained a university degree or have successfully completed Higher Vocational Training (HBO). You produce project analyses in your field easily and you are thorough when it comes to implementation. You have strong oral and written communication skills. Your command of English is excellent.
Further information:
For more information about this position you can contact Ineke Jonker - Hoogerkamp, Ph.D, Business Unit Manager, at phone +31 (0)71 - 524 40 00 or by email (ineke.jonker@xendo.com).
What we offer:
We offer a varied position within a young and fast-growing company. We offer an attractive salary with good fringe benefits.
Your reaction:
If you are interested in this position, we invite you to send your curriculum vitae and motivation, stating the above vacancy number, to:
Xendo Pharma Services B.V.
attention of HRM Department
Postbus 255
2300 AGÂ Leiden
or email to:
