Location

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

Check out Your Career in Drug Product Services at Lonza! This is a fully site‑based role.

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. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits

What you will do:

• Independently execute, coordinate and review physico-chemical and biochemical assays under cGMP according to existing method SOPs (e.g. Compendial testing/content/identity/purity for small molecules, biologics/large molecules).
• Document assay execution under cGMP following Good Documentation Practices (GDP) and flag relevant observations to the supervisor for further assessment.
• Accountable for execution of operational tasks in the lab such as mobile phase preparations, calibration of equipment, adherence to and maintenance of 6S, consumable management and support of equipment maintenance.
• Support validation and transfer activities in frame of new project introduction, cGMP standards for audit readiness and supports onsite customer/regulatory audits.
• Assist in investigation/troubleshooting for assigned tasks.

What we are looking for:

• First hands‑on experience in analytical methodologies like pH measurement, UV‑Vis, turbidity; experience with HPLC, ELISA or similar technologies is a plus.
• Experience with GMP is a plus.
• Apprenticeship or equivalent in Analytical Chemistry, Biochemistry or related field.
• Fluency in written and spoken English; German is an asset.
• You enjoy routine analytical testing and look for a chance to set up and shape a brand new laboratory with us.

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