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 at