Specialist* OQA GMP Compliance & Master Records

at  BioNTech AG

JOIN OUR TEAM OF PIONEERS!

As a part of our team of more than 5.000 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.

• Ensure overall GMP-Compliance of the site KBT
• Contribute that controlled documents are well documented, reviewd and approved by QA, with includes beach records of diverse projects and manufacturing steps
• Support the design and review of quality processes, documents and templates used for the review and release of GMP products
• Supervision of change control, deviations and CAPAs
• Support self-inspections and routine check