Associate Director, Global Quality Engineering
Leverage your expertise in quality assurance to drive growth and innovation at Lonza.
* Owning all quality-related responsibilities for new facilities, equipment, and utilities related to GMP manufacturing of biologics & APIs.
* Coordinating with team members to ensure projects are completed on time and with compliance mindset.
* Overseeing department operations, hiring, and terminating staff members as needed.
* Managing day-to-day operations within the department, providing direction as needed.
* Monitoring industry trends and sharing information with colleagues to stay relevant.
* Developing long-term strategies for the Visp Project Portfolio, including setting goals and plans.
Key Requirements:
* Master of Science in Bio-Engineering or a related field.
* Experience working in a GMP-related environment in the pharmaceutical industry.
* Proficient work experience in a Quality Unit (ideally within Biologics or Cell Gene).
* Execution of CAPEX, green-field experience an advantage.
* Regulatory inspections experience.
* Leadership experience an advantage.
* Project Management and Stakeholder Management certification an advantage.
* Fluent English, German language skills an advantage.
Join a company that respects and protects its people and environment. Achieve business results while upholding ethics and making a meaningful difference globally.