About this role
About the Role:
As an MSAT Supervisor in Downstream Processing, you will play a critical role in supporting tech transfer, process validation, and optimization for biopharmaceutical production. You will act as the process owner during the PPQ stage and work closely with cross-functional teams to ensure the successful execution of projects. This role provides an exciting opportunity to contribute to BioNTech’s innovative therapies while strengthening downstream technical capabilities within the MSAT team.
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Your Contribution:
- Apply expertise in facilities, process flow, tech transfer, and Process Performance Qualification (PPQ) to support manufacturing operations
- Manage daily manufacturing activities, including deviation investigations, CAPA implementation, change control, and drafting/approval of technical plans and reports
- Act as the process owner during the PPQ stage and support continuous process optimization and validation efforts
- Contribute to cross-border tech transfers to various CDMOs or production sites
- Collaborate with relevant departments to ensure smooth project execution according to timelines and quality standards
- Support downstream talent development initiatives within the MSAT team
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A Good Match:
- Familiarity with GMP production processes, with hands-on experience in tech transfer and process validation
- Demonstrated experience in MSAT or Process Development (PD) within biopharmaceuticals
- Ability to read and write technical documents fluently in both Chinese and English
- Basic proficiency in English communication for effective teamwork across global teams
- Strong organizational skills with attention to detail; capable of managing complex tasks efficiently
- A proactive mindset with excellent problem-solving skills