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

Lead the GMP-compliant qualification and re‑qualification of a great variety of analytical instruments and software in our QC laboratory. At our growing site, this position provides exceptional opportunities to learn, contribute, and make a meaningful impact. Check out your career in Quality Control!

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:

• Lead and manage the initial qualification and re-qualification of analytical equipment and software in our QC laboratory (HPLC, CE, refrigerators etc.)

• Execution of performance qualification and act as a trainer for defined equipment and related processes

• Author, review and approve documentation (qualification plans and reports; documents from service providers) related to laboratory systems as required

• Ensure compliance of laboratory systems according to cGMP and current standard processes and regulatory guidelines as well as respective SOP`s.

• Oversight and guidance for proper maintenance and qualified state of equipment; Performing period review of qualification/calibration of analytical equipment and act as system owner for defined Equipment

• Participate as Subject Matter Expert in audits and inspections

What we are looking for:

• Solid work experience in the GMP-controlled Quality Control laboratory is a must

• Hands-on experience in qualification of analytical instruments is a must

• Apprenticeship or academical degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field

• Broad experience in analytical methodologies like e.g. HPLC, ICief, UV-VIS, Elisa, CE-SDS is an advantage. Knowledge of lab quality systems like LIMS, Tiamo or Empower/Chromeleon is a plus

• Fluency in written and spoken English is a must, Language skills in German is a plus

• You enjoy working independently and in a dynamic & fast-pacing project environment

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.