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. Global Process Engineer MS&T The process engineer MS&T DS is a member of the team of process owners for Drug Substances, all modalities. In this function the position holder takes ownership for commercial or late clinical stage manufacturing process(es) by gathering and providing process knowledge and historical information to all internal and external interfaces. He is accountable and responsible for making decisions regarding maintenance and further development of the process, oversees internal/external manufacturers performance, address Health Authorities requests, drives investigations and changes impacting the manufacturing process throughout late clinic and commercial life cycle. Process ownership for commercial and late clinical stage manufacturing processes Creation and maintenance of process templates; supervision of internal and external manufacturers performances throughout the life cycle Leading Subject Matter Expert for the processes in close alignment with internal departments (e.g. AS&T, tech Dev., Regulatory Affairs, QA) and external partners Drive continuous improvement to enhance process robustness; monitoring of KPIs in collaboration with internal stakeholders (e.g. sites, development), network partners as well as CMOs Investigate and solve process issues, be the link to all internal departments, sites and manufacturing network partners Support in commercial scale-up activities, tech transfers and launches & harmonization topics between different manufacturing sites, incl. support of GxP documentation for regulatory submissions University degree in natural sciences or engineering 3 to 5 years of practical experience in the life science industry and expertise in process engineering (Upstream, downstream, cell & gene, plasmid) Experience in technology transfers of biotech products Profound knowledge of EU / US GMP guidelines and regulatory standards Creativity and the ability to develop a flexible approaches to changing conditions High team spirit; excellent collaborating skills and ability to work in a high dynamic work environment Good communication skills, fluency in German and English 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.