Registration Manager Europe-International- The Netherlands

One of the biggest global pharmaceutical companies is looking for a Registration Manager Europe who will be part of the international life cycle management team. You will be the right hand of the Head Regulatory to prepare the strategy and submit marketing authorization in Europe. I know the manager will give you a lot of autonomy and you will be able to get more experience internationally.

Profile:

• Master Degree in life sciences, preferably Pharmaceutical Sciences
• Minimum 3 years experience in Regulatory Affairs
• Knowledge of Regulatory Requirements in EMEA
• Technical systems skills (e.g. word processing, spreadsheets, databases, online research)
• Project management skills: multiple projects and deadlines
• Excellent spoken and written English is required

You will be responsible for a big product portfolio of products with a good reputation on the market. This means that you will have enough work and can use your project management skills to coordinate other departments. Accordingly, you have a helicopter view.

The company values their employees and will give support to get comfortable in the team and with the products. You will divide the tasks within a big team which means you can learn from each other.

Interviews are happening now so if this job appeals to you please send me, Annelies De Baere, your most recent CV in Word format to a.baere@nonstop-recruitment.com or call me on +32 2 403 49 80. If you are not interested and you know someone else, do not hesitate to pass on their contact details.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.

What I offer: As a specialist Headhunter within Regulatory Affairs for the pharmaceutical industry in Belgium I have a strong market knowledge and good relationships within companies. Therefore I will not just find you suitable roles but also offer you accurate, honest advice and provide you with inside information on the team/company culture.

Key words: Regulatory Affairs/Regelgeving/life cycle management/MAA/CTD/eCTD/Regulering/Marketing Authorization/Manager/Specialist/Expert/Associate/ /RA/English/Pharmaceutical/pharmaceuticals/pharma/The Netherlands/Nederland/Amsterdam/Nederlands