Director, Site Quality Head Drug Product Stücki 80-100%
Lonza, Ridgeland, SC, United States
The actual location of this job is in Basel Stücki, Switzerland.
For our successful Drug Product (DP) focused branch located in Basel, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Director, Site Quality Head Drug Product position.
What you will get:
An agile career and a dynamic work culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
What you will do:
Lead the overall Quality strategy for the Basel Stücki Drug Product site and guide the long‑term Quality roadmap
Partner with the senior leadership team to ensure site functions are aligned with Quality priorities
Oversee and enhance the local Quality System while supporting global Quality System development
Oversee the Quality Control teams, ensuring performance, alignment, and strong delivery of objectives
Drive continuous improvement initiatives and track progress against key site quality KPIs
Build and develop strong Quality expertise across teams, ensuring independence and compliance
Ensure audit and inspection readiness at all times and meet regulatory commitments on schedule
What we are looking for:
Master’s or PhD degree, or equivalent experience, in Life Sciences, Quality Management, or a related field, incl. Eligibility as a Responsible/Qualified Person in Switzerland
10+ years of Quality experience in pharmaceutical and cGMP environments
Strong experience in biological drug substance and drug product Quality Control and Fill & Finish operations
Deep knowledge of Swiss, EU, and US GMP requirements, including compliance, inspection, and validation expectations
Strong understanding of chemical and biological drug product development and manufacturing
Demonstrated ability to lead a team, inspire a strong quality culture and drive continuous improvement
Strong business acumen with proven ability to align Quality strategies to organizational objectives
Exceptional communication and stakeholder‑management skills, with the ability to influence at all levels, including senior management. Fluent in English and German is a must
About Lonza 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.
Ready to shape the future of life sciences? Apply now. #J-18808-Ljbffr
For our successful Drug Product (DP) focused branch located in Basel, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the Director, Site Quality Head Drug Product position.
What you will get:
An agile career and a dynamic work culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
What you will do:
Lead the overall Quality strategy for the Basel Stücki Drug Product site and guide the long‑term Quality roadmap
Partner with the senior leadership team to ensure site functions are aligned with Quality priorities
Oversee and enhance the local Quality System while supporting global Quality System development
Oversee the Quality Control teams, ensuring performance, alignment, and strong delivery of objectives
Drive continuous improvement initiatives and track progress against key site quality KPIs
Build and develop strong Quality expertise across teams, ensuring independence and compliance
Ensure audit and inspection readiness at all times and meet regulatory commitments on schedule
What we are looking for:
Master’s or PhD degree, or equivalent experience, in Life Sciences, Quality Management, or a related field, incl. Eligibility as a Responsible/Qualified Person in Switzerland
10+ years of Quality experience in pharmaceutical and cGMP environments
Strong experience in biological drug substance and drug product Quality Control and Fill & Finish operations
Deep knowledge of Swiss, EU, and US GMP requirements, including compliance, inspection, and validation expectations
Strong understanding of chemical and biological drug product development and manufacturing
Demonstrated ability to lead a team, inspire a strong quality culture and drive continuous improvement
Strong business acumen with proven ability to align Quality strategies to organizational objectives
Exceptional communication and stakeholder‑management skills, with the ability to influence at all levels, including senior management. Fluent in English and German is a must
About Lonza 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.
Ready to shape the future of life sciences? Apply now. #J-18808-Ljbffr