Associate* Operational Quality Assurance Laboratories (m/w/d)

Become a member of the BioNTech Family!

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.

The Associate* Quality Assurance will join a highly motivated and well-coordinated team responsible for supporting BioNTech's internally GCP for labs regulated laboratories. In this role, the Associate* Quality Assurance will play a crucial part in enabling the laboratories to operate in a well-functioning regulated environment and in swiftly resolving any current quality-related issues or processes.

This position is located in the Global Development Quality Assurance department and will bring you in contact with questions in a Quality Management System working in GCP for Labs and CAP/CLIA. Furthermore, you will have the opportunity to connect with many different functional departments and possess a high visibility within the company.

Your Main Responsibilities Are:

• Support the Team of QA Managers and Specialists in administrative and organizational tasks
• Planning of quality related activities (Planning and management of internal Audits) on behalf of the team
• Support the Team in Quality Follow Up Activities and management of timlines
• Management of QA Projects
• Act as a training officer to coordinate the training landscape of the team
• Support in Document Management and Document Reviews

What You Have to Offer:

• Vocational training or Bachelor's degree in a scientific or technical discipline
• First experience (at least 6 month) in quality assurance within the pharmaceutical or biotech industry
• Quality mindset and first knowledge of handling regulatory guidelines/guidance documents
• Resilient personality, ability to connect people and distribute information
• Strong communication and presentation skills in both German and English
• Basic knowledge of project management and the use of project management tools is advantageous
• High carefulness and accuracy in the way of working, conscientiousness, and detail-orientation

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.