Aristo Group is seeking a Batch Record Reviewer in Luzern, Switzerland. This role supports clinical biologics manufacturing by ensuring compliance with ALCOA+, GDP, and GMP standards through operational reviews and documentation management. The ideal candidate has a degree
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 role focuses on right‑first‑time
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 manufacturing by
Michael Page International (Switzerland) SA is seeking a Batch Record Review Specialist in Luzern, Switzerland. The successful candidate will be responsible for ensuring the accuracy and compliance of batch records in clinical biologics manufacturing. Applicants should have a bachelor’s degree
Aristo Group is seeking a GMP Documentation Specialist in Luzern, Switzerland, to support clinical biologics manufacturing. This role involves reviewing executed batch records, ensuring compliance with ALCOA+ standards, and aiding in documentation creation and lifecycle support. The ideal
Operator for Biotech Support Operations For one of our clients, an international pharmaceutical company, we are seeking an Operator for Biotech Support Operations . General Information: Start date: ASAP (high urgency) End Date: 1 year Home
Operator for Biotech Support Operations For one of our clients, an international pharmaceutical company, we are seeking an Operator for Biotech Support Operations . General Information: Start date: ASAP (high urgency) End Date: 1 year Home
# 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
80–100%, GMP / Sterilproduktion, Quality Assurance Für einen etablierten Schweizer Produktionsstandort der pharmazeutischen Industrie mit Fokus auf sterile Arzneimittel suchen wir eine erfahrene Persönlichkeit im Bereich Qualitätssicherung, die ihre fachliche Expertise einbringen möchte – ohne disziplinarische
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 Operations and
Print Team Lead Overview The Global Clinical Supply (GCS) organization manages the end-to-end clinical supply for the company’s portfolio. GCS is accountable for the planning, sourcing, labelling, packaging and delivery of clinical supplies to clinical sites