Intern QC Small Molecules 80-100%
lonza.com
- Job written in
- English
- Location
- Visp
- Work type
- On-site
- Type
- Internship
Lonza, a global leader in life‑science manufacturing, is looking for an Intern QC Small Molecules to join its Quality Control team in Visp, Switzerland. The position sits within a GMP‑ and ISO‑controlled setting and focuses on ensuring compliance while supporting laboratory operations. The intern will assist QC II labs in upholding GMP, ISO and internal quality standards. Daily tasks include helping with corrective‑and‑preventive action (CAPA) execution, managing investigations, and closing quality events promptly. The role also involves collaborating with lab staff to spot and apply continuous‑improvement ideas, promoting data‑integrity practices, and supporting 6S initiatives to keep the workspace orderly. Preparing audit‑related documents, SOPs and training material, as well as taking part in GEMBA walks, are also part of the routine. Candidates should hold a Bachelor's or Master's degree in Life Sciences, Chemistry, Pharmacy, Biotechnology, Quality Management, Engineering or a closely related discipline. A genuine enthusiasm for quality control, compliance and regulated environments is essential, together with strong organisational abilities and clear communication in English. The job requires a proactive attitude, a keen eye for detail, and the capacity to cooperate effectively with cross‑functional and laboratory teams. Fluency in German is mandatory. Working on‑site in Visp enables real‑time interaction with colleagues and direct contribution to the high‑quality production of medicines. Lonza offers an inclusive culture, a dynamic work atmosphere and performance‑linked compensation, alongside benefits that vary by role and location. The internship provides hands‑on exposure to QC processes, audit preparation and continuous‑improvement projects, laying a solid foundation for a career in regulated quality environments. What the role asks for: - Bachelor's or Master's degree in a relevant scientific or engineering field - Strong interest in quality control, compliance and regulated settings - Excellent organisational and communication skills in English - Proactive mindset with passion for continuous improvement - Ability to work with cross‑functional and laboratory teams - Strong attention to detail and commitment to quality - Mandatory proficiency in German (spoken and written) - Basic understanding of GMP regulations (nice‑to‑have)
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