The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Are you ready to be part of an exceptionally ambitious project? In our Drug Product Services (DPS) business unit, we are currently seeking a Process Expert for our new aseptic Drug Product Manufacturing facility in Stein. This role is part of a Greenfield project, where you will join a highly energized and diverse team. Your contributions will be crucial in ensuring our processes are executed safely within the expected quality and compliance (cGMP).

What you will get:

• An agile career and a dynamic work culture.

• An inclusive and ethical workplace.

• Compensation programs that recognize high performance.

In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below.

• Benefits in Stein: https://bit.ly/42DlBDk

What you will do:

• As the technical expert you ensure that the aseptic fill & finish line (including lyophilization step) runs efficiently and effectively

• Coordinate and support the qualification and validation activities, ensuring they meet strict industry standards

• Lead product and process related investigations and deviations and define CAPAs and changes.

• Identify weaknesses in the production line, investigate issue and determine solutions. Drive process related trouble shooting / investigations ensure that process technical batches generate sufficient process knowledge by thoroughly testing critical variables

• Provide front line shopfloor support to manufacturing, working with the operator, focusing on manufacturing process

• Establish, drive and maintain good cleanroom management practices . Collaborate with team members to successfully implement improvements and new processes

• Achieve Inspection readiness level and to provide the necessary support in any internal or external audit

What we are looking for:

• Proven experience in EITHER aseptic filling or aseptic manufacturing of drug product

• Experience with lyophilization process is an advantage

• Experience with qualification and validation of manufacturing equipment is a strong advantage

• Degree or equivalent experience in Life Science or Engineering

• Demonstrated experience working in a GMP-controlled environment is a must

• Proficiency in English; German is a plus

• Ability to agilely move between various tasks during this dynamic and exciting project phase. You demonstrates strong collaboration skills and actively support your team members

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.