Become a member of the BioNTech Family!
As a part of our team of more than 4.000 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.
Senior DMPK Scientist* as (Associate) Director* Non-Clinical Safety & DMPK
At BioNTech, you will contribute to non-clinical development and safety activities for global R&D programs and new technology platforms during different stages of pharmaceutical development by implementing strategic drug metabolism and pharmacokinetics (DMPK) paths. BioNTech is expanding its activities towards new therapeutic modalities in different disease areas. You will enable clinical translation of our first-in-class immunotherapeutics and vaccines by assessing DMPK properties of diverse modalities such as mRNA therapeutics, biologics and ADC.
Your main responsibilities are
- Design, execute and report ADME/PK studies, analyzing and interpreting data, and presenting findings and advice back to project teams
- Recommending and leading new strategies within DMPK to develop and implement state-of-the-art technologies
- Aligning program-specific and platform overarching pharmacokinetic activities in cross-functional teams with pre-clinical and clinical stakeholders
- Authoring and review of critical modules for submission packages (Investigator Brochure, IND, scientific advices, regulatory requests)
- Partnering with research leads for the design and data analysis/interpretation of pharmacokinetic (PK), toxicokinetic (TK) and pharmacodynamic (PD) aspects of preclinical studies
- Engage with CROs and external consultants regarding conduct and interpretation of non-clinical DMPK studies.
What you have to offer
- Degree in life sciences, pharmacy, bioanalytical sciences, pharmacokinetics or equivalent. Preferably advanced degree incl. PhD/MD/VMD
- Several years of experience in the biotechnology or pharmaceutical industry including strong knowledge of DMPK in the early and late drug development process
- Strong research background with interest in translating data into insights and recommendations.
- Experience in leading DMPK activities in drug development programs in Oncology and/or Infectious diseases from first-in-human to market authorization in a matrix organisation.
- Proficient in using Phoenix WinNonlin for PK/PD modeling. Familiarity with other software like Simcyp, PK-Sim, Monolix, R, MATLAB is a plus.
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 4475 (please indicate for inquiries)
We look forward to your application!
- BioNTech does not differentiate on the basis of gender, political opinion, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important – it’s a match!
BioNTech - As unique as you www.biontech.com