Associate Director* Regulatory Affairs CMC (FixVac)

  • Mainz
  • Work experience
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Become a member of the BioNTech Family!

As a part of our team of more than 2.500 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.
We aim to reduce the suffering of people with life-changing therapies by harnessing the potential of the immune system to develop novel therapies against cancer and infectious diseases. While doing so, we are guided by our three company values: united, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives.

Associate Director* Regulatory Affairs CMC (FixVac)

In this position, you will lead all aspects of Regulatory Affairs CMC for Investigational Medicinal Products in a clinical development program of the oncology FixVac platform in order to bring new medicinal products on the market. As you guide the products along this exciting path, you will establish new regulatory routes and define requirements for these next generations of therapeutics. You will also get the opportunity to act globally and work cross-functionally.

Your main responsibilities are:
  • Act as global regulatory CMC lead for assigned development projects and ensure all regulatory submissions and CMC projects are aligned with the  Regulatory CMC Strategy from pre-clinical stage up to (including) marketing authorisation
  • Plan, prepare and conduct all CMC related aspects for interactions with national authorities and supra-national agencies (e.g., MPA, PEI, EMA, FDA, as well as WHO when relevant) in the scope of product development incl. market authorisation
  • Lead and manage high quality regulatory CMC content of regulatory applications and dossiers for product development including marketing authorisation; coordinate preparation, authoring and review of documents and dossiers
  • Set up, adjust and continuously optimize regulatory CMC processes and interfaces (internal and external) to ensure regulatory success; manage regulatory compliance activities
  • Monitor changes and evolution in the regulatory CMC landscape for therapeutics (Regulatory Intelligence); analyse the impact of drug changing regulations for BioNTech's products

What you have to offer.

  • Degree in pharmacy, chemistry, biology, biochemistry, or equivalent
  • At least 5 years professional experience in Global Regulatory Affairs CMC during clinical development and/or registration for Biologics, Vaccines and/or Small Molecules
  • Extensive experience in preparation and revision of regulatory CMC documents
  • Knowledge of CMC drug development (Drug Substance and Drug Product) and knowledge of multidisciplinary functions involved in drug development and manufacturing
  • Good combination of strategic and operational skills; ability to make flexible, but thorough decisions in a highly dynamic environment
  • Excellent communication skills in English

Benefits for you.

  • Company Pension Scheme
  • Childcare
  • Jobticket
  • Company Bike
  • Leave Account
  • Fitness Courses
  • Mobile Office
  • Special Vacation
... and much more.

Have we kindled your pioneering spirit?

Then apply now for our location Mainz and simply send us your application documents using our online form.

If you have any further questions, our Talent Acquisition Team will be happy to answer them on + 49 (0) 6131-9084-1291 (monday-friday, from 12 noon to 4 pm).

Job-ID 6417 (please indicate for inquiries)

We look forward to your application!

*BioNTech does not differentiate on the basis of gender, race or ethnicity, religion, color, sexual orientation or identity, disability, age and other protected statuses as given by applicable law. We are committed to creating a diverse environment and are proud to be an equal opportunity employer. Most important – it’s a match!

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