Cinfa Biotech is the biosimilar company of the Spanish Cinfa Group. We develop,
manufacture and commercialise high-quality biosimilars. Our goal is to achieve a
premier position within the global biosimilar market. We do our business on a fully
integrated level, combining our specialist expertise in early- and late-stage biosimilar
development and in global commercialisation of biosimilars.
Do you want to be part of the regulatory team bringing new biosimilars to the market?
We are looking to strengthen our team in Munich, Germany.
Your responsibility will be to provide major contributions in the registration process of
our products. You interact closely with your colleagues in the technical and clinical
development departments. In this environment you will actively shape dossier
preparation processes and have a strong impact on submission procedures.
To be successful in your role, you have a scientific or pharmaceutical background and
have several years of experience in technical or medical writing with special focus on
registration dossiers. Ideally you are familiar with lifecycle management of
registrations and have expertise in the communication with regulatory authorities.
From your experience, you know how to successfully work in an international team
together with colleagues from other departments and backgrounds. Through a mix of
diligence and communication skills, you provide the ability to compile complex dossier
sections and to communicate with external partners and regulatory authorities.
Our offer to you is to be part of a successful and growing team with a high degree of
flexibility and freedom to further your career in the development of biosimilars.
Become a part of our biosimilars story and help us building long-term success!
We look forward to your application.
Cinfa Biotech GmbH
Nymphenburger Str. 3c
Cinfa Biotech S.L.