Manager* Nonclinical Safety

  • Mainz
  • Research, development, teaching

Become a member of the BioNTech Family!

As a part of our team of more than 1.500 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age: Amongst multiple programs in the pipeline, we are conducting research on a Covid-19 vaccine in our project “Lightspeed” based on our mRNA-technologies. Furthermore, we are pioneers in the development of individualized cancer therapies and in the combat against other diseases.
 
We aim to achieve life-changing successes for patients by being innovative, passionate and united,so 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.

Manager* Nonclinical Safety

At BioNTech, you will be responsible for the safety assessment of our most important platforms in collaboration with lead scientists that enable clinical translation of our first-in-class immunotherapeutics. 
Your main responsibilities are:
  • Responsible for the execution of an integrated nonclinical development strategy from target assessment to early and late clinical development
  • Supervising and monitoring of in vitro and in vivo PD/PK/toxicology studies at contract research organizations
  • Generating and reviewing safety assessment reports and documentation for internal decision making, as well as regulatory submissions to health authorities and approval processes in all phases of drug development
  • Steering nonclinical safety evaluations of development candidates in cross-functional teams in BioNTech as well as externally with consultants and collaboration partners
  • Active contribution and representation of nonclincial safety aspects in program development teams

What you have to offer.

  • You have a degree (PhD/MD/VMD) in Natural or Life Sciences. Demonstrated experience in drug development
  • Knowledge of immunotherapy and infectious disease or oncology, as well as advanced experience in all areas of toxicology
  • You have at least 3 - 5 years of experience in the biopharmaceutical industry and have been involved in clinical trial applications of biologics and/or ATMPs. Regular interactions with health authorities have been part of your job
  • Board certification in Toxicology such as ERT/DABT is highly desirable, as well as solid technical expertise and operational experience in managing CROs
  • You are a team player, have excellent english communication skills and love to work in multidisciplinary teams

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, Anna Flister will be happy to answer them on + 49 (0) 6131-9084-1291 (monday-friday, from 12 noon).

*BioNTech does not differentiate on the basis of gender, race, religion, color, origin, sexual orientation, disability, age and other protected status as required by applicable law. We are committed to creating a diverse environment and are proud to be an equal opportunity employer.

BioNTech - As unique as you

https://biontech.de