Specialist* Manufacturing Processes New iNeST Operations
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.
Specialist* Manufacturing Processes New iNeST Operations
At the iNeST facility, cancer therapeutics will be produced individually for each patient in order to meet their personal needs. The role of Specialist Manufacturing Processes New iNeST supports the daily operations in production to enable smooth production. As support for the subject matter experts (SMEs), the role holder possesses in-depth process knowledge in the areas of DNA production, RNA production, lipoplexation, fill & finish, or visual inspection. Tasks include root cause analysis and risk assessment for process deviations and the definition of corrective and preventive measures. The Specialist Manufacturing Processes New iNeST coordinates change control.
Your main responsibilities are:
- Support for subject matter experts (SMEs) regarding product and process knowledge for the production of individualized cancer therapy (DNA production, RNA production, lipoplexation, fill & finish, or visual inspection) during the project phase
- Handling of deviations occurring during the production process
- Creation of area-specific documents (e.g. SOPs, working procedures, forms)
- Definition and implementation of corrective and preventive actions (CAPA management)
- Coordination of change procedures in production (Change Owner)
What you have to offer:
- University degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/scientific area
- 2 years of experience in manufacturing/production or relevant experience, ideally in a biotech or pharmaceutical company
- Good knowledge of EU GMP regulations
- General understanding of technical processes
- High carefulness and accuracy in the way of working, conscientiousness, and detail-orientation
- Refined colloquial and correspondence skills in English and ideally also in German
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 6529 (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