Specialist* Operational Quality Assurance - Supplier Qualifications
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.
Specialist* Operational Quality Assurance - Supplier Qualifications
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.
Benefits for you:
- Flexible Working Time
- Mobile Office
- Work from EU Countries (up to 20 days per year)
- Company Pension Scheme
- Childcare
- Jobticket
- Company Bike
- Leave Account
- Fitness Courses
... and much more.
Have we kindled your pioneering spirit?
Then apply now for our location Mainz Goldgrube 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 6891 (please indicate for inquiries)
We look forward to your application!
*BioNTech does not tolerate discrimination, favoritism, or harassment based on gender, political opinion, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important – it’s a match!
BioNTech - As unique as you
www.biontech.com