Role: Senior Biotechnologist responsible for designing, optimizing, and scaling biologics and advanced therapy processes in a regulated biopharmaceutical environment.
Key Responsibilities:
- Develop robust upstream and/or downstream bioprocesses for biologics/advanced therapies.
- Lead tech transfer into GMP manufacturing.
- Support process characterization, validation, and regulatory documentation.
- Troubleshoot complex technical issues across biologics/ATMP workflows.
- Apply data-driven, QbD-based approaches to improve process performance and reliability.
- Partner with global, cross-functional teams to deliver safety, quality, and patient-focused outcomes.
- Mentor and guide scientists while maintaining strong scientific rigor.
Qualifications/Skills: Strong expertise in bioprocess development and scale-up, GMP tech transfer, process characterization and validation, regulatory support, and collaborative problem-solving in regulated environments.