Associate Director* QA - Pharmacovigilance

  • Mainz
  • Work experience
  • Medicine, Pharmacy, Laboratory
  • Quality Management, Quality Assurance
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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 do research on a Covid-19 vaccine in our project “Lightspeed” based on our mRNA-technologies. Furthermore, we are pioneering in the development of individualized cancer therapies and in the combat against other diseases.
 
By being innovative, passionate and united, we aim to achieve life-changing successes for patients. If you like to engage in creating hope for a healthy future in many people´s lives, we should get to know each other!

Associate Director* QA - Pharmacovigilance

As Associate Director* QA - Pharmacovigilance, you will add value by being a PV expert within our QA department, guiding through audits and inspections, and bringing PV systems to the next level. Your main responsibilities are:
  • Contribute to the development and continuous improvement of necessary PV systems to assure compliance to worldwide regulations and corporate policies
  • Plan and execute the PV audit program (internal and vendor audits) and work with auditees to resolve any identified non-compliances
  • Actively participate in and support PV inspections, onsite or remote, to ensure that PV inspections are a success; support the resolution of findings by working with PV business partners
  • Promote continuous education with regards to PV regulations and expectations - for yourself and BioNTech staff
  • Contribute to PSMF, PV SOPs and other PV-related documents

What you have to offer.

  • Completed scientific or medical-technical training (BTA, CTA or MTA) or scientific university degree
  • Extended experience with pharmacovigilance systems in the pharmaceutical industry and in-depth knowledge of the relevant regulations (especially GVP)
  • Experience with electronic document management systems (DMS) and databases
  • Practical experience in the field of quality assurance / quality management
  • Reliability, organizational talent and confidence in usage MS Office programs
  • Fluent in English language (spoken and written)

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, 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, religion, color, origin, sexual orientation, disability, age and other protected status as required by applicable law. We are committed to creating a diverse environment and are proud to be an equal opportunity employer.

BioNTech - As unique as you

https://biontech.de