(Senior) Scientist (m/w/d) Quality Control, Environmental Monitoring
lonza.com
- Job written in
- English
- Location
- Visp
- Work type
- On-site
- Type
- Full-time
The position of (Senior) Scientist, Quality Control, Environmental Monitoring is based at Lonza's Visp site in Switzerland. Lonza operates a globally connected network of facilities that produce medicines under strict GMP standards, and the role supports the company's mission to deliver safe, high‑quality therapeutics. In this capacity you will gather and analyse monitoring data with systems such as MODA, LIMS and other digital tools, then compile concise reports. You will record all GMP‑related actions, lead investigations when alerts or excursions occur, and conduct root‑cause analyses while coordinating corrective steps with relevant stakeholders. Drafting, reviewing and approving DMS documentation to maintain compliance, refining monitoring workflows for better data integrity, and handling MODA changes under change‑control are also key tasks. During audits, inspections or customer visits you will represent the team confidently. The ideal candidate holds a university degree in life sciences or a comparable scientific discipline and brings roughly two years of experience working in a GMP‑regulated setting. Proficiency with Microsoft Office and familiarity with electronic documentation platforms are required, as is the ability to communicate fluently in English. The role calls for an independent work style and a proactive, detail‑oriented approach to problem solving. Lonza offers an agile scientific career in a collaborative, ethical environment that values continuous learning. Employees benefit from competitive local packages, relocation support for eligible candidates and their families, and exposure to cross‑functional projects and regulatory interactions. The Visp location provides a modern workplace where diverse perspectives are encouraged, and the team culture emphasizes accountability and excellence. What the role asks for: - Degree in life sciences or related scientific field - Approximately 2 years experience in GMP‑regulated environment - Strong digital competence with Microsoft Office and documentation systems - Fluent English communication skills - Experience in environmental monitoring or microbiology (nice-to-have) - Knowledge of regulatory requirements, pharmacopoeias, EU Annex 1 (nice-to-have) - German language ability (nice-to-have) - Proactive, detail‑oriented, solution‑focused mindset (nice-to-have)
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