Lonza AG
Associate Director, Manufacturing - BPMSS L1L2
📍 CH - Visp
Role and responsibilities
Take full end-to-end accountability for manufacturing activities, ensuring high-quality project execution, on-time batch release, and adherence to safety and compliance standards. Lead and mentor a team of production leaders (chemists/biologists) and the Batch Review Team. Collaborate with Technical Operations, MSAT, Supply Chain, and Quality Assurance to streamline processes. Develop and implement manufacturing strategies aligned with company goals. Oversee daily manufacturing operations to ensure production targets are met and resources are efficiently deployed. Drive continuous improvement initiatives, including CAPEX projects for new technologies and equipment. Act as a member of the leadership team and deputy to the Head of Operations Asset.
Team / description
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Qualifications and Skills
Completed university degree (Master’s degree or PhD preferred) in engineering, biotechnology, or a related field
At least 8 years of professional experience in pharmaceutical or biotechnological manufacturing, including a minimum of 3 years in a leadership role with a focus on process management or related field
Strong understanding of manufacturing processes and workflows in the biopharmaceutical industry
Proven experience in leading system implementation and optimization projects
Strong analytical skills and problem-solving abilities
Excellent communication and presentation skills in both German and English, written and verbal
Demonstrated leadership skills with the ability to motivate and develop teams
Familiarity with data integrity requirements and regulatory standards (e.g., FDA, EMA)