Take a leading technical role in developing and implementing Process Analytical Technologies (PAT) for real-time analytics and process control in biopharmaceutical manufacturing.
Compensation
Salary Range: 44.000,00 € - 81.800,00 €
Responsibilities
Implement high-throughput approaches for real-time bioprocess monitoring and optimization, leveraging automation, online analytics and advanced data analysis.
Lead technology development and continuous improvement initiatives supporting process intensification.
Develop and deploy spectroscopy-based Process Analytical Technology methods, including Raman and dielectric spectroscopies.
Support the implementation of innovative technologies that advance manufacturing processes and operational performance.
Interpret spectral data and establish secure data management and analysis procedures aligned with Good Manufacturing Practice requirements.
Bring your biotech and data expertise to the heart of biopharmaceutical manufacturing. As a Biotech Engineer/PAT Specialist, you will take a leading technical role in developing and implementing Process Analytical Technologies (PAT) for real-time analytics and process control.
Compensation
Expected Annual Base Salary Range for role: € 44,000 to € 81,800
Responsibilities
Implement high-throughput approaches for real-time bioprocess monitoring and optimization, leveraging automation, online analytics and advanced data analysis.
Lead technology development and continuous improvement initiatives supporting process intensification.
Develop and deploy spectroscopy-based Process Analytical Technology methods, including Raman and dielectric spectroscopies.
Support the implementation of innovative technologies that advance manufacturing processes and operational performance.
Interpret spectral data and establish secure data management and analysis procedures aligned with Good Manufacturing Practice requirements.
Requirements
University degree in Biotechnology, Chemical Engineering or a related scientific field.
Nice to have: Raman spectroscopy
Nice to have: online biomass monitoring
Nice to have: technology integration in GMP environments
The Associate Principal Scientist will contribute to CMC development of the company's pipeline, leading the design, development, and optimization of cell culture processes and the transfer of processes to clinical and commercial manufacturing sites.
Compensation
$142,000 - $224,100
Responsibilities
Participates in andor leads upstream process development of first-in-human and commercial processes by efficiently developing high yield, robust, and scalable cell culture processes.
Responsible for process development, process characterization, and regulatory filing activities to ensure a smooth and clear path to successful PPQs and BLAs for the company's pipeline.
Partner with colleagues in Discovery, Cell Line, Downstream Process Development, Analytical Sciences, and Manufacturing to develop integrated clinical and commercial process and manufacturing solutions that achieve quality by design targets with robust control strategies.
Advancing the upstream platform processes through creative process improvement initiatives to increase operational efficiency and reduce costs.
Collaborate with academia, industry partners, and vendors to drive development, innovation, and adoption of new process technologies.
Requirements
Ph.D. with 4+ years' experience
Master's with 8+ years' experience in chemical engineering, Bioengineering, Biological Engineering, or a related field
