# 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
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
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. The
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,
