Specialist Operational Quality Assurance - Supplier Qualifications (all genders)

Mainz, Germany   |   full time   |   Job ID: 6891 

 

 

Specialist Operational Quality Assurance – Supplier Qualifications

 

As Specialist Operational Quality Assurance – Supplier Qualifications you will act as a general point of contact for QA relevant topics such as oversight of suppliers, service providers and contract labs. You will be part of the Lifecycle Manager Supplier and Material department, reporting to the Associate Director Operation Quality Assurance Suppliers. You will deal with supplier qualifications and auditing as well as generating the oversight about quality events of suppliers and the respective follow up plans. Furthermore, you will closely work with our Material Qualification team, with the Supplier Complaint team and various other local stakeholders. As our groundbreaking individualized vaccines against cancer products take large steps towards registrational studies and later commercialization, this role is a key element of our plans to expand material supply chain.

 

Your main responsibilities are: 

  • Strengthen our oversight of suppliers, service providers and contract labs
  • Perform/support Audits, Supplier Qualifications
  • Follow up on Quality Events, Audit findings and CAPA plans of suppliers
  • Participate in Performance evaluation of suppliers and contract labs
  • Participate in building a robust Material Supply Chain 
  • Support the OQA LM Supplier Team
  • Alignment with different stakeholder groups

 

What you have to offer: 

  • University degree in Chemistry, Pharmacy, Biology, Molecular Biology, or other scientific area or completed medical-technical training or a comparable qualification
  • Initial work experience in quality assurance or quality oversight ideally in a biotech or pharmaceutical company
  • Talent for organizational work; interest for working in a highly dynamic and flexible environment
  • Willingness to travel for audits
  • Quality mindset and knowledge of EU GMP and FDA regulations for clinical manufacturing
  • Communication and presentation skills in both German and English
  • High team spirit and excellent collaborating skills

 

 

Your Benefits:

 

It's our priority to support you:

  • Your flexibility: flexible hours | vacation account  
  • Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning
  • Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential
  • Your health and lifestyle: Company bike
  • Your mobility: Job ticket | Deutschlandticket 
  • Your life phases: Employer-funded pension | Childcare 

 

 

Apply now - We look forward to your application!

 

Apply to our Mainz, Germany location by sending us your documents via our online form. For any questions, contact our talent acquisition team on: + 49 (0) 6781 9855 211 (Monday-Friday from 12 PM to 4 PM CET).

 

Job ID 6891 (please always specify if you have any questions)   

 

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your Recruiter.

 

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BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!  

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