Associate Director* Quality Assurance

Mainz, Germany

Job Description

Senior, very experienced
Quality Management, Quality Assurance

Become a member of the BioNTech Family!

As a part of our team of more than 1.500 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age: Amongst multiple programs in the pipeline, we are conducting research on a Covid-19 vaccine in our project “Lightspeed” based on our mRNA-technologies. Furthermore, we are pioneers in the development of individualized cancer therapies and in the combat against other diseases.

We aim to achieve life-changing successes for patients by being innovative, passionate and united,so 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 Director* Quality Assurance - Joint Ventures East Asia

As Associate Director Quality Assurance (QA) for Strategic Partnerships, you will be making a meaningful contribution to the ongoing development of our RNA production processes. In this role, you will support us on our mission as the interface to the BioNTech business partners in China and the USA, and ensure Good Manufacturing Practice (GMP)-compliant manufacturing of commercialized medicinal products.

Your main responsibilities will be:
  • Executing the transfer of QA-specific knowhow during the product implementation / transfer to a new manufacturing site and during the production phase
  • Supporting on upcoming quality topics, e.g. deviations (Provide input, create contact to experts, follow up on actions, etc.)
  • Leading regular / attend irregular meetings with joint venture partners (incl. preparation, agenda, minutes, follow up on actions, etc.)
  • Supporting the GMP-compliant implementation and improvement of quality management at joint ventures, including the establishing and monitoring of KPIs
  • Reviewing and approving documentation regarding the joint ventures to assure GMP-compliance

What you have to offer.

We are looking for an enthusiastic, committed, and visionary individual, ideally with the following characteristics:
  • University degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/scientific area
  • Multiple years of work experience in quality assurance, quality oversight or relevant experience, ideally in a biotech or pharmaceutical company
  • Experience managing work in both team setting and independently
  • Profound knowledge of relevant Chinese, US & EU regulations, EMA, FDA, NMPA, and other regulatory standards as well as Good Manufacturing Practice
  • Effective collaboration, coordination and stakeholder management skills, both in cross-functional internal and external matrix team environment
  • Good combination of strategic and operational skills; ability to make flexible, but thorough decisions in a highly dynamic environment
  • High carefulness and accuracy in the way of working, conscientiousness and detail-orientation
  • Refined colloquial and correspondence skills in both German and English; presentation skills adaptable to all levels of internal and external stakeholders

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, Johanna Diehl will be happy to answer them on + 49 (0) 6131-9084-1291 (monday-friday, from 12 noon).

  • 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!

BioNTech - As unique as you

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Job Detail

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    Mainz, Germany
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