GC International AG, based in Lucerne, is looking for a motivated Supply Chain Coordinator (f/m/d) to join their team. This role is critical in ensuring efficient execution of global supply chain operations. You will coordinate end-to-end
Garmin Italy Technologies is now boarding a C/C++ Software Developer enrolled in L.68/99 lists. You are self-motivated, goal-oriented, and a strong team player willing to actively contribute to the success of the team by providing technical
An innovative company with a global presence Proven track record in batch record review About Our Client For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking
# Senior Administrative AssociateApplyremote type: Hybridlocations: CHE - Lucerne - Lucerne (Rösslimatt)time type: Full timeposted on: Posted Todaytime left to apply: End Date: June 10, 2026 (14 days left to apply)job requisition id: R Job DescriptionWe
# Senior Administrative AssociateApplyremote type: Hybridlocations: CHE - Lucerne - Lucerne (Rösslimatt)time type: Full timeposted on: Posted Todaytime left to apply: End Date: June 10, 2026 (14 days left to apply)job requisition id: R Job DescriptionWe
Garmin Italy Technologies is now boarding C++ Software Developers! You are self-motivated, goal-oriented, and a strong team player who is willing to be an active contributor to the success of the team by providing technical solutions
Garmin Italy Technologies is searching for talented and passionate C++ Software developers! You are self-motivated, goal-oriented and strong team player who is willing to be an active contributor to the success of the team, providing technical
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
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
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.
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
Who We Are GC International AG, based in Lucerne, is a global leader in dental care and oral health. With more than 100 years of history, presence in over 100 countries, and a team of over