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
# 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
Job Summary Responsible for leading and governing Phase In / Phase Out (PIPO) initiatives across the product lifecycle to ensure controlled product changes and PIPO transitions, from a Supply chain perspective with a strong focus on
About the Role To strengthen our Supply Chain team in Lucerne, we are looking for a motivated and detail-oriented Supply Chain Coordinator (f/m/d) - full time or part-time 40-60%. The Supply Chain Coordinator (f/m/d) plays a
Job Description Our Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that’s devoted
# Senior Specialist Compliance Excellence (m/f/d)Applyremote type: Not Applicablelocations: CHE - Lucerne - Schachen (Werthenstein)time type: Full timeposted on: Posted Todaytime left to apply: End Date: June 26, 2026 (15 days left to apply)job requisition id: