Was ist meine Funktion? Sie übernehmen das Steuer für technische Kunden- und Engineering-Projekte – von A bis Z Sie begleiten Projekte durchgängig: von der ersten Idee über smarte technische Specs bis zum finalen Go-live Sie haben den
# Director, Global Clinical Supply ComplianceApplyremote type: Hybridlocations: CHE - Lucerne - Schachen (Werthenstein)time type: Full timeposted on: Posted Todaytime left to apply: End Date: August 13, 2026 (14 days left to apply)job requisition id: R
Temporary 12 month contract // 100% Onsite in Lucern // Start: 1.Sept About Our Client Prestigious pharmaceutical company Job Description Set up, practical execution and troubleshooting of downstream processes under Good Manufacturing Practices (GMP) Knowledge of
The Quality Assurance Engineer is responsible for for the development, implementation and verification of the Quality Assurance requirements. Quality Assurance Engineer will act as main interface to Process Engineering and Operations for quality and safety topics. The Quality
For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking an Associate Specialist within the Downstream Operations group. As a member of the manufacturing team at our clients company, you
Associate Specialist Downstream Operations (m/f/d) Where Science Meets Purpose Join a Team Shaping Tomorrows Therapies Duration: 12 months (temporary assignment) About Our Client Our client is an internationally active, innovation-driven biotech company based in the greater
Brunel Switzerland is seeking a Quality Assurance Engineer to develop, implement and verify QA requirements at the manufacturing site. You will act as main interface to Process Engineering and Operations on quality and safety topics. Responsibilities include defining