Pharmaceutical Scientist - CMC Project Coordination (m/f/d)- BioNTech SE

☞ jobvector GmbH

Vue: 182

Jour de mise à jour: 07-10-2024

Localisation: Mainz Rhineland-Palatinate

Catégorie: Science La main doeuvre

Industrie: Information Technology Services Biotechnology Pharmaceuticals

Niveau: Mid-Senior level

Type d’emploi: Full-time

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le contenu du travail

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.

CMC Project Coordinator*

Your Main Responsibilities Are

At BioNTech, you will be responsible for supporting scientific development sub-projects and early stage projects from pre-clinical to clinical stage.
  • Collaborate with CMC experts, technical leads and expertise areas to develop detailed CMC sub-project plans required to successfully progress an asset from pre-clinical through clinical phases
  • Lead the scientific assessment of project related to specific CMC aspects in collaboration with the CMC project lead
  • Manage CMC timelines and budget for the respective sub-project as well as coordinate and manage communication with internal and external partners
  • Drive timely and data-driven decision making, and facilitate scientific discussions within CMC and with external partners to inform product development
  • Support the CMC Experts and the department in administrative and organisatorial aspects
  • Advanced Degree (MS/PhD) in Pharmacy, Chemistry, Biopharmaceuticals, Biochemistry or Biology with professional experience in an international, pharmaceutical environment
  • Sound knowledge of working in scientific/technical CMC development functions (process development, pharmaceutical and/or analytical development, manufacturing). Documented experience in CMC regulatory affairs would be a plus
  • Solid CMC development knowledge in either early or late stage projects with good understanding of all stages of drug development; Experience with regulatory filings for biologicals (IND/IMPD, BLA/MAA) is considered a plus
  • Excellent communication and negotiation skills and ability to clearly and concisely communicate complex technical matters; Experience defining and executing strategy is required
  • Company Pension Scheme
  • Childcare
  • Jobticket
  • Company Bike
  • Leave Account
  • Fitness Courses
  • Mobile Office
  • Special Vacation
... and much more.
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Date limite: 21-11-2024

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