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

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 Visp: https://bit.ly/3wjkoFi

What you will do:

• Collect, evaluate, and summarize data in MODA and LIMS, using digital tools to interpret results and confirm conclusions.

• Document GMP‑relevant activities and lead investigations of alert or action level excursions.

• Drive root‑cause investigations and align corrective measures with key stakeholders.

• Create, review, and approve DMS documents to ensure accuracy, completeness, and compliance.

• Improve QC monitoring processes to enhance data quality, efficiency, and robustness.

• Implement QC monitoring updates and manage MODA‑related changes under change‑control procedures.

• Represent the team during inspections, audits, and customer visits with clear and confident communication.

What we are looking for:

• A degree in life sciences (biology, microbiology, pharmacy, or related field) with relevant experience.

• 3–5 years of relevant experience in a GMP-regulated environment in Environmental Monitoring and/or Microbiology .

• Strong digital skills, including experience with Microsoft Office and documentation systems.

• Knowledge of regulatory requirements, including pharmacopoeias and EU Annex 1.

• Flexibility, independence, and readiness to adapt to changing priorities.

• A proactive, solution‑oriented mindset with strong attention to detail.

• Strong communication skills in English; German skills are an advantage.