Join Our Team at Lonza
Today, Lonza is a global leader in life sciences, operating across three continents. While we excel in science, there’s no magical formula to our success. Our greatest asset is our talented people working together, generating ideas that not only help businesses thrive but also enhance the lives of individuals. In return, we empower our employees to take charge of their careers, allowing their big and small ideas to genuinely improve the world. That's the kind of work we invite you to be a part of.
Position Overview
As a member of the MSAT (Manufacturing Science & Technology) Team at Ibex Visp, you will play a crucial role in the successful transfer, scale-up, supervision, and optimization of biopharma processes. Your expertise in process science and manufacturing will enable you to significantly contribute to the development of the MSAT toolbox while sharing the long-term responsibilities of a process owner.
Key Responsibilities
- Secure success during technology transfer by applying formal processes and tools to manage the transfer of information, process-related risks, and change control.
- Manage technical risks associated with process transfers, identification, and introduction of new raw materials while aligning project completion with management goals.
- Collaborate cross-functionally to ensure communication of critical process and technical information to meet required deadlines and customer outcomes.
- Act as the interface between the process donor (customer, process development) and operations, ensuring process scalability and manufacturability.
- Resolve process issues that arise during manufacturing while complying with all regulatory requirements.
- Execute GMP risk analysis for manufacturing processes and implement these processes in the plant.
- Provide independent 24/7 on-plant technical support, process monitoring, and complex data analysis according to the team roster.
- Interact directly with customers during tech transfers, campaign preparation, execution, and closure, including daily reporting of batch status and performance.
- Ensure timely compilation of process-related deviations, change requests, and campaign reports.
- Compile CMC sections in filing documents and the technical content of validation reports.
- Contribute to the development and implementation of standardized MSAT procedures and processes.
- Lead technical investigations to ensure continuous improvements are made to processes and operations.
- Challenge the status quo and seek opportunities for improvements across the business.
- Act as a mentor for scientific and production staff in various fields of expertise.
- Share information and knowledge generously with other teams and functions, demonstrating high integrity.
Key Requirements
- Bachelor’s, Master’s, or PhD degree in biotechnology, chemical engineering, or related disciplines.
- Working experience in biopharma manufacturing and/or process development, preferably in Mammalian Manufacturing.
- Experience in technology transfer for Mammalian Manufacturing (preferred).
- Understanding of GMP and bioprocess technology.
- Excellent communication skills with the ability to interact effectively with various stakeholders.
- Fluency in English.
Why Join Us?
Each day, Lonza's products and services positively impact millions of people worldwide. This responsibility drives us to achieve our business results ethically and respectfully, safeguarding both our people and the environment. At Lonza, we believe that the journey toward success should uphold our values and integrity.
Individuals choose Lonza for the challenge and opportunity to creatively solve complex problems and develop groundbreaking ideas in life sciences. In return, we offer the satisfaction derived from making a meaningful difference in lives across the globe.
Apply online using the form below. Please note, only applications matching the job profile will be considered.