Job Description The Director in Global Clinical Supply (GCS) Compliance is a technical leader responsible for governing and advancing GCS’s global GxP Quality Systems to ensure the organization executes clinical supply operations in a compliant, inspection‑ready,
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
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
Prestigious pharmaceutical company 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
# 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
