GMP Manufacturing Technician

About YouThe successful candidate will have an educational background in a relevant discipline and 2-5 years of experience in the pharmaceutical or biotech industry. A minimum of 2 years of practical experience in the GMP manufacturing of biologics (upstream or downstream) is required.Expert knowledge in specific unit operations for biologics...

About the RoleWe are seeking an experienced professional to join our growing manufacturing team at Aristo Group. As a member of this team, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of early-phase clinical therapies.The ideal candidate will have a strong understanding of GMP principles and...

About This OpportunityWe are seeking a highly motivated Manufacturing Operations Specialist to join our team in Lucerne, Switzerland.The selected candidate will be responsible for implementing and maintaining GMP manufacturing processes for early-phase clinical therapies.Main ResponsibilitiesPrepare and maintain SOPs and electronic master batch records while...

Associate Manufacturing Operations SpecialistThis is a(n) (Associate) Specialist position within the Manufacturing Operations group at our company in the greater Lucerne area. This position requires full-time physical presence at the site to support manufacturing and to enable optimal integration into an existing team.As a member of the growing manufacturing...

The selected candidate will be responsible for the following task area:Executes and troubleshoots manufacturing processes under GMP regulationsEnsures compliance with GMP and EHS standardsDocuments process execution, deviations, and changes; collaborate with Quality AssuranceSupports process improvements and new technology implementationManages SOPs, batch...

About the RoleThis full-time, on-site position is focused on setting up, executing, and troubleshooting upstream, downstream, and support unit operations in continuous and fed-batch manufacturing processes under GMP guidelines.Executing process execution, deviations, changes, and CAPAs while collaborating with Quality Assurance and other internal...

Job DescriptionThis role is responsible for supporting various activities related to the implementation and GMP manufacturing of early-phase clinical therapies.The successful candidate will have a strong background in a relevant discipline and a minimum of 2-5 years of work experience in the pharmaceutical or biotech industry.A key aspect of this position is...

What We're Looking ForWe are looking for an experienced professional with a strong background in a relevant discipline and a minimum of 2-5 years of work experience in the pharmaceutical or biotech industry.A key aspect of this position is the ability to work efficiently as part of a team, as well as willingness to take responsibility for independent...

Role OverviewAbout Our ClientWe are a global leader in the pharmaceutical industry seeking a skilled Specialist to join our Manufacturing Operations team in Switzerland.This full-time role offers an exciting opportunity to contribute to the implementation and GMP manufacturing of early-phase clinical therapies in a collaborative environment.Key...

Jobdescription We are looking for a Process Engineer - II - P2 Specialist, Manufacturing Operations to join the Manufacturing Operations team for one of our clients. This full-time, on-site position is focused on supporting GMP manufacturing activities and ensuring seamless integration within the existing team.Contract: Temporary contract via Randstad...

job detailsWe are looking for a Process Engineer - II - P2 Specialist, Manufacturing Operations to join the Manufacturing Operations team for one of our clients. This full-time, on-site position is focused on supporting GMP manufacturing activities and ensuring seamless integration within the existing team.Contract: Temporary contract via RandstadStart Date:...

We are looking for a Process Engineer - II - P2 Specialist, Manufacturing Operations to join the Manufacturing Operations team for one of our clients. This full-time, on-site position is focused on supporting GMP manufacturing activities and ensuring seamless integration within the existing team.Contract: Temporary contract via RandstadStart Date: ASAPEnd...

Key ResponsibilitiesSet up, practical execution and troubleshooting of upstream, downstream and support unit operations in continuous manufacturing and fed-batch processes under Good Manufacturing Practices (GMP)Management and documentation of process execution, deviations, changes and CAPAs. Partnering with Quality Assurance and other internal stakeholders...

Job OverviewWe are seeking a highly skilled Process Engineer to join our Manufacturing Operations team for one of our clients. The ideal candidate will be responsible for supporting GMP manufacturing activities and ensuring seamless integration within the existing team.

Job DescriptionA challenging position is available in our Manufacturing Operations department for a dedicated Specialist.The ideal candidate will have hands-on experience with quality management systems such as Trackwise, SAP QM, or VeevaVault.Main TasksDrive process optimization initiatives and support the integration of new technologies through non-GMP...

Our client, a leading company in the pharmaceutical industry based in Lucerne is looking for aLab Technician Scientist in a QC Bioassay Lab-Start date: 3/1/2025-Planned duration: 12 months-Extension: RecurringThe integrated Biologics Analytical Department provides support to the Biotechnology Department by performing release and stability testing of...

Our client, a leading company in the pharmaceutical industry based in Lucerne is looking for aLab Technician Scientist in a QC Bioassay Lab-Start date: 3/1/2025-Planned duration: 12 months-Extension: RecurringThe integrated Biologics Analytical Department provides support to the Biotechnology Department by performing release and stability testing of...

JobdescriptionFor one of our clients, a leading pharmaceutical company, we are looking for a Senior Technical Transfer EngineerGeneral Information:Start date: 01.04.2025End date: 31.12.2025Extension: possible (to be discussed)Workload: 100%Workplace: Lucerne, SwitzerlandHome office: the position will be primarily home-based (for the candidates based in...

CBRE Global Workplace Solutions erbringt mit mehr als 60'000 Mitarbeitenden integrierte Facility Management Services auf allen Kontinenten. In der Schweiz ist der Bereich GWS mit technischen, infrastrukturellen und kaufmännischen Facility Management Leistungen für Kunden aus verschiedenen Branchen tätig. Für unsere wachsende Facility Management...

CBRE Global Workplace Solutions erbringt mit mehr als 60'000 Mitarbeitenden integrierte Facility Management Services auf allen Kontinenten. In der Schweiz ist der Bereich GWS mit technischen, infrastrukturellen und kaufmännischen Facility Management Leistungen für Kunden aus verschiedenen Branchen tätig. Für unsere wachsende Facility Management...