Management Jobs in Visp, Schweiz

“Project Manager role in Visp, Switzerland, requiring engineering/science/business degree, German fluency, and PMP/Prince2 certification. Office-first with 20% remote flexibility. Focus on strategic improvements, change management, and stakeholder leadership in biotech/pharma environment.”

“Regular job offer in Visp, Switzerland for a QC Small Molecules role requiring a Bachelor's or Master's degree in Life Sciences/Chemistry. Focus on GMP compliance, data integrity, and laboratory excellence. German and English required. Competitive compensation.”

“Full-time QA Sterility Assurance Lead role in Visp, Switzerland for (COMPANY NAME), requiring expertise in microbial control and sterility assurance in pharmaceuticals. Offers relocation assistance, competitive compensation, and benefits. Focus on contamination control, regulatory compliance, and leadership in aseptic processing.”

“(COMPANY NAME) seeks an OE Manager in Visp, Switzerland to drive Operational Excellence via Lean/Six Sigma, lead cross-functional projects, and improve business performance. Requires proven CI experience, leadership, and stakeholder management. Relocation assistance available.”

“(COMPANY NAME) seeks a Training Manager (m/f/d) for Large Scale Small Molecules in a GMP-regulated pharmaceutical environment. Role involves developing training curricula, facilitating sessions, and ensuring compliance. Requires GMP knowledge, LMS experience, and fluency in German. Offers dynamic career growth in life sciences.”

“Full-time office-based Project Planner (CAPEX) role at (COMPANY NAME) for 5-8+ years experienced professionals. Manages large capital projects (>CHF 20M) using Primavera P6/MS Project. Requires pharma/biotech/CDMO experience, strong analytical skills, and collaboration in global teams. Office-first with 20% remote flexibility.”

“Full-time role in Visp, Switzerland for (COMPANY NAME) as MSAT Material Management & Single-Use Systems Expert (80%-100%). Requires Master's/PhD in biotech/engineering, GMP expertise, and cross-functional collaboration. Offers career growth, benefits, and impact on biopharmaceutical manufacturing.”

“Full-time QA Manager role in Visp, Switzerland (80-100%) for (COMPANY NAME), ensuring GxP compliance, reviewing QC documents, and supporting regulatory audits. Requires pharmaceutical QA/QC experience, cGMP knowledge, and strong communication skills in English (German advantageous).”