MSAT Expert Drug Product

MSAT Expert Drug Product

Lonza

Visp, Switzerland

What you will do:

• Responsible for implementing the manufacturing process in the plant, as received from DP process development or the customer.
• Lead and/or participate in cross-functional teams as an MSAT expert. This includes the lifecycle of assigned projects, from planning through coordination, implementation, control, and completion, aligned with project management goals.
• Act as technical counterpart to commercial and clinical customer.
• Owner of concepts for process controls and important areas within manufacturing.
• Act as singe-point-of-contact for operational topics within the Lonza network.
• Prepare and perform qualification and validation activities in compliance with cGMP regulations and specification requirements.
• Contribute to the development and implementation of standardized MSAT procedures and processes.
• Responsible for continuous improvement of process performance and product quality.
• Proactively anticipate, evaluate, and resolve scientific and technical challenges
• Act as a mentor for scientific and production staff across various fields of expertise.
• Manage process monitoring and process control strategies, including complex data analysis.

What we are looking for:

• Preferred area of study: Pharmaceutical Technology, Biotechnology, Chemistry, Process Engineering, or a related scientific discipline.
• More than 3 years of experience in manufacturing and/or MSAT, Development or QA/QC.
• Fluency in English (spoken and written).
• Proven understanding of aseptic manufacturing processes (pharmaceutical and regulatory aspects) is an advantage.
• Strong communication skills and ability to interact with various internal and external stakeholders.
• Clear team orientation and ability to collaborate across functional groups.
• Structured, focused, and well-organized working style.