Associate* Clinical Trial Supply Management / GxP Compliance

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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* Clinical Trial Supply Management / GxP Compliance

At BioNTech, you will support our Clinical Trial Supply Management department in several administrative and organizational tasks in a GxP regulated environment. Your main responsibilities are:
  • Support as operational expert in GxP-related tasks across diverse clinical trials and R&D Programs (e.g., Packaging and Labeling, Shelf Life Extension, Sponsor Release, Product Specification Files, TMF Filing, Material Safety Data Sheets, Temperature Excursion Management, Logistics) including project-related/project-independent GxP documentation and filing thereof
  • Support in preparation of quality documents (e.g., deviations, changes, CAPAs)
  • Operate with internal and external partners to make sure that Clinical Trial Supply Management activities meet relevant legislation and international GxP guidelines (e.g.Coordination and execution of orders)
  • Maintenance of trackers for for Clinical Trial Supply Management activities under BNT`s responsibility

What you have to offer.

  • Completed vocational training in the administrative, technical, biological or commercial field or comparable qualification (e.g. bachelor degree)
  • First work experiences as a study or team assistant in a GxP (GCP, GMP, GDP) regulated environment
  • Knowledge in relevant legislation and international GxP guidelines would be beneficial
  • First experiences in processing GxP-related documents, e.g. evaluation of temperature excursion reports, preparation of batch specific documentation, Deviations, Changes, CAPAs, would be beneficial
  • Profound skills in the application of standard software (e.g. MS Office)
  • Business-professional English language skills, German language skills are a plus
  • Able to accurately work under pressure in a versatile environment, very reliable and diligent way of working, independent and proactive way of working, excellent organizational and communicative skills, enjoys working in a team

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 5314 (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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