Director, MSAT Upstream Laboratory Lead

As a Senior Manager for the MSAT Upstream Laboratory, you will provide scientific and strategic leadership to advance BioNTech’s antibody and ADC programs. You will play a critical role in designing, developing, and qualifying upstream processes while fostering innovation and continuous improvement in late‑stage development and commercialization. In this role, you will lead a collaborative team environment, working closely with internal departments such as Process Development, Analytical Development, Quality, Regulatory Affairs, and external partners to ensure seamless technology transfers and GMP readiness.

Your expertise will directly support BioNTech’s mission to deliver high‑quality therapies to patients worldwide.

• Provide scientific and strategic leadership for the Gaithersburg MSAT Upstream Laboratory
• Collaborate across teams (Supply Chain, Process Development, AS&T, Analytical Development, Quality, Regulatory) to establish and run the MSAT Upstream Laboratory operations
• Develop phase‑appropriate upstream scale‑down models for antibody programs
• Lead knowledge and technology transfers for antibody and ADC programs to enable upstream characterization, investigational studies, and scale‑down model execution
• Coach and develop MSAT team members on upstream antibody manufacturing processes while fostering a culture of scientific rigor and continuous improvement
• Design, develop, characterize, qualify upstream processes including cell processing, culture/expansion, harvest, cryopreservation
• Draft SOPs, reports, presentations; maintain instrumentation/equipment; troubleshoot issues as needed
• Collaborate with internal teams and external groups to advance late‑stage antibody capabilities; contribute to PPQ protocol/report authoring ensuring GMP compliance and scientific rigor

• Master’s degree in Biochemical Engineering, Chemical Engineering, Biomedical Engineering or related discipline with 12+ years of pharmaceutical/biotechnology process development industry experience
• In‑depth CMC knowledge in early or late‑stage antibody technology transfer projects with sound understanding of all stages of antibody drug development (GMP/QbD approach)
• Proven success leading cross‑functional CMC teams with strong organizational skills and stakeholder/client management expertise
• Experience as subject matter expert for antibody upstream processes including technology transfer projects/product commercialization
• Demonstrated ability to design complex projects while shaping scientific strategy at both platform/program levels
• Strong collaboration skills across GMP Manufacturing, Quality Control/Assurance teams within technology transfer projects

Preferred qualifications:

PhD in a relevant field

US based candidates expected Pay Range: $168,100 - $268,700/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.