About Our Client For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking a Batch Record Review Specialist (m/f/d). In this role, you will support clinical biologics
Overview Are you passionate about quality, precision, and working in a GMP-regulated environment? We are currently seeking a detail-oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment.
# Associate Director, Planning & Scheduling (m/f/d)Applyremote type: Not Applicablelocations: CHE - Lucerne - Schachen (Werthenstein)time type: Full timeposted on: Posted Todaytime left to apply: End Date: June 13, 2026 (14 days left to apply)job requisition
The Batch Record Reviewer supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation meets ALCOA+ , GDP , and GMP expectations. As part of the Manufacturing Operational Excellence team, this
The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ standards and GMP expectations. The role is part of the Operational Excellence team within Manufacturing
Job description Docpier Salary: CHF 100000 – 130000 per year. Closing date: Requirements Mehrjährige Erfahrung mit Cloud‑Plattformen (Azure, AWS oder GCP). Fundiertes Wissen in Infrastrukturautomatisierung (Terraform, Kubernetes, CI/CD). Erfahrung mit Logging‑, Monitoring‑ und Alerting‑Systemen (z. B. Prometheus,
