Provide technical support for commercial manufacturing of biologic drug substances at external manufacturing sites (CMOs)
Support technology transfer activities between manufacturing sites and external partners
Troubleshoot process-related issues, support deviation investigations, change controls, and process optimization
Monitor manufacturing activities, identify operational risks, and ensure timely resolution of technical issues
Collaborate closely with Manufacturing, Quality, Supply Chain, and cross-functional technical teams
Ensure effective communication with internal stakeholders and external manufacturing partners
Maintain GMP compliance and support high-quality commercial manufacturing operations

MSc or BSc in Biotechnology, Biochemistry, Chemical Engineering, or a related scientific discipline
Proven experience in GMP biopharmaceutical manufacturing, ideally within the biologics industry
Strong knowledge of mammalian cell culture, downstream purification, and manufacturing processes
Experience in technology transfer, process support, déviation management, and continuous improvement
Excellent problem-solving, communication, and stakeholder management skills
Ability to work independently in a dynamic, cross-functional, and international environment

External Manufacturing MS&T

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