Administrator* GxP Compliance

  • Mainz
  • Junior, Career start
  • Office, administration, processing
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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.

Administrator* GxP Compliance

The Administrator* GxP Compliance is a reliable support of the Clinical Trial Supply Management (CTSM) department members in administrative tasks.  He/She is responsible for preparation of trial-related and trial-independent GxP documentation, generation of back-ups and filing thereof, maintenance of trackers, lists and templates.

Main duties:
  • Independent performance of administrative and organizational tasks within the CTSM department.
  • Filing of trial-related documentation concerning clinical trial supply activities e.g. in the Trial Master File (TMF) or electronic Trial Master File (eTMF).
  • Perform quality checks for e.g. TMF-relevant documentation in TMF or eTMF concerning clinical trial supply activities.
  • Maintain overview lists for GxP relevant documentation concerning clinical trial supply activities including proactive status tracking.

What you have to offer.

  • Relevant work experiences as a study or team assistant in a GxP (GCP, GMP, GDP) regulated environment.
  • Profound skills in the application of standard software (e.g., MS Office).
  • Experiences with filing of clinical trial documentation, e.g., Trial Master File, would be beneficial.
  • Business-professional German and English language skills
  • Able to accurately work under pressure in a versatile environment.
  • Very reliable and diligent way of working.
  • Strong Quality awareness.
  • Excellent organizational and communicative skills.

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  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 7566 (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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