Regulatory Affairs Biologics-Flexible Working Times-Home Office

My client is a medium-sized Biotech company, who is currently developing new Niche Biologics drugs. The company was found circa 10 years ago, and thank to his employee-friendly environment now counts more than 1000 people.

However, they are not stopping growing! Namely the Registration team is looking for a new Regulatory Affairs Manager (m/w).

In this company your family management benefit from flexible working times and some home office days, so that putting together work and career on daily basis is very easy.

This will allow you to have a very high quality of life, as you do not have to renounce to your private life in order to make a strong career in the very promising area of Large Molecules, that can ensure you a great professional stability!

Your core activities:

• Composition of Pre-Approval Registration Dossiers for international submissions
• Life Cycle Management
• Reply to Deficiency letters from Authorities
• Database and Registration Systems Management

Contract Type: You will be hired directly by my client

Salary: Negotiable upon experience

Location: Frankfurt-Heidelberg Area

Starting Datum: ASAP

If you feel interested in principle, do not hesitate to get in touch with me

Desired Requirements:

• Experience in writing dossiers for drugs in Pre-Approval
• High command of English language
• Ability to work in EU without any visa or sponsorship

Happy to recommend someone? If you want to recommend someone, and we manage to place your referral, you will get a small 'thank you' gift from us!

Due to the high number of application we could be not able to come back to you, if your requirements are too distant from the one requested above. We thank you in advance for your understanding

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