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K-Recruiting Life Sciences seeks a GMP Quality OPS practitioner in Switzerland to support compliance-based programs and QOS activities. You will participate in batch release support and critical program issue resolution, and conduct documentation reviews to ensure GMP compliance.
The role emphasizes adherence to high quality standards, cross-functional collaboration, and timely execution in a regulated environment. Start date is 01.11.2026 for a 24-month assignment in the Luzern area.
The Global Development Quality OPS team is responsible to drive or support compliance-based programs and results which include support cross functional projects, solving simple problems, current Good Manufacturing Practices (cGMP) quality initiatives, quality system improvements, quality directives, compliance metrics and monitoring, SOP management, and site procedures.
Start: 01.11.2026
Duration: 24 months