For one of our clients, a leading global pharmaceutical company, we are currently looking for a Qualification and Validation Manager.General Information:Start date: 05.01.2026Duration: until 30.09.2026Workplace: BaselWorkload: 100%Remote/Home Office: possible, max 20%Working hours: StandardDepartment: MSAT (MMNGF)Team: 10 peopleAbout the job:The Qualification Manager is responsible for the CSV and qualification program at Basel DS Manufacturing, as well
For one of our clients, a leading global pharmaceutical company, we are currently looking for a Qualification and Validation Manager.General Information:Start date: 05.01.2026Duration: until 30.09.2026Workplace: BaselWorkload: 100%Remote/Home Office: possible, max 20%Working hours: StandardDepartment: MSAT (MMNGF)Team: 10 peopleAbout the job:The Qualification Manager is responsible for the CSV and qualification program at Basel DS Manufacturing, as well
Are you an experienced treasury expert? Do you have experience in coordinating and delivering and leading the implementation of the treasury module. Then please find the job description below:Tasks & Responsibilities:Design and develop concepts for SAP Treasury and InHauseBankIT implementation Lead for related Treasury systemsAlign with developers to ensure deliverables are on track and according to requirementsAdvice Divisional IT team in the region's
Are you an experienced treasury expert? Do you have experience in coordinating and delivering and leading the implementation of the treasury module. Then please find the job description below:Tasks & Responsibilities:Design and develop concepts for SAP Treasury and InHauseBankIT implementation Lead for related Treasury systemsAlign with developers to ensure deliverables are on track and according to requirementsAdvice Divisional IT team in the region's
For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Medical Device Clinical Safety Scientist.The primary responsibility of this role is to support clinical investigations of MDs by developing and providing safety input into core MD clinical investigation documents, including the Clinical Investigation Plan (CIP/Protocol), Investigator’s Brochure (IB), and Reference Safety Information (RSI). The role holder is
For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Medical Device Clinical Safety Scientist.The primary responsibility of this role is to support clinical investigations of MDs by developing and providing safety input into core MD clinical investigation documents, including the Clinical Investigation Plan (CIP/Protocol), Investigator’s Brochure (IB), and Reference Safety Information (RSI). The role holder is
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