Derzeit 5 offene Stellen für diese Kriterien.

Change Control Manager (m/f/d)

Global External Manufacturing is the competence center for parts and products in the diagnostic workflow, manufactured by external suppliers. This includes the development of new products, product care activities, the assurance of supply as well as the supplier selection and maintenance in close collaboration with Procurement.

The perfect candidate is someone who has knowledge and experience in GMP regulations and practices. Furthermore the candidate demonstrates flexibility, adaptability, proactivity and process thinking.

Test Engineer (m/w/d)

Unser Kunde sucht einen Testingenieur (m/w/d) mit nachweislicher Erfahrung in Systemtests und technischer Dokumentation, der für die Planung, Durchführung und Dokumentation von Integrationstests verantwortlich ist und die Einhaltung regulatorischer und projektspezifischer Anforderungen sicherstellt.

PCB-Layout-Entwickler:in - ECAD Xpedition (m/w/d)

Quality Assurance Manager Drug Product (m/f/d)

As part of the Synthetic Molecules IMP Quality Group, the QA Manager plays a key role in ensuring robust quality oversight for Synthetic Molecules Drug Substance and Drug Product operations, including associated quality control activities. Embedded within the IMP Quality Organisation Switzerland, this position is responsible for safeguarding GMP compliance and driving continuous quality improvement at the Drug Product IMP manufacturing facility at the Basel site.

The ideal candidate holds a Master’s degree in a scientific discipline and brings over 10 years of experience in the pharmaceutical industry, including a minimum of 5 years in Quality Assurance. A strong understanding of cGMP requirements and quality standards across clinical development phases is essential, along with a proven track record of successfully supporting regulatory inspections.

Fluency in both German and English is mandatory

Process Engineer (m/w/d)

Als Process Engineer im Manufacturing liefern Sie Lösungen für den USP, DSP oder ADC-Bereich bei Basel Drug Substance Manufacturing für eine sichere und qualitativ hochwertige Produktion. Sie dienen sowohl unseren Patienten als auch unseren Mitarbeitern im Manufacturing Unit, indem Sie Prozessverbesserungen entwickeln und implementieren.