Aktuelle Jobs im Zusammenhang mit Pharmaceutical Operations Lead - Basel, Basel-Stadt - ITech Consult AG
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Biomarker Clinical Operations Lead
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Biomarker Clinical Operations Lead In Pdg
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Packaging Operations Lead
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Analytical Operations Lead
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Pharmaceutical Packaging Manager
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GMP Pharmaceutical Specialist
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Global Clinical Program Lead
vor 6 Minuten
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Biomarker Operations Project Lead
Vor 4 Tagen
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Head of Pharmaceutical Research and Development
Vor 3 Tagen
Basel, Basel-Stadt, Schweiz Roche VollzeitAbout Roche's MissionWe foster diversity, equity, and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people's varied healthcare needs.Job OverviewThis Head of Pharmaceutical Research and Development role will...
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Clinical Operations Director
vor 8 Stunden
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Pharmaceutical Development Manager
Vor 3 Tagen
Basel, Basel-Stadt, Schweiz Novartis Farmacéutica Vollzeit**Job Overview:**We are seeking a skilled Pharmaceutical Development Manager to join our team at Novartis Farmacéutica.About the Role:The Pharmaceutical Development Manager will be responsible for leading and overseeing analytical activities throughout drug development within a global project team.Develop and implement analytical strategies to meet quality,...
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Pharmaceutical Quality Expert
Vor 5 Tagen
Basel, Basel-Stadt, Schweiz Actalent VollzeitJoin our team as a Pharmaceutical Quality Expert and contribute to the development of innovative solutions that drive excellence in quality assurance. In this role, you will be responsible for ensuring the compliance and continuous improvement of GMP standards across all IMP production facilities.About the Role:The Synthetic Molecules IMP Quality Group is...
Pharmaceutical Operations Lead
vor 2 Wochen
The role of Medical Alliance Operations Leader at ITech Consult AG involves leading the development and implementation of clinical research processes for drugs and devices. This includes establishing process infrastructures, monitoring and managing clinical research processes, and ensuring compliance with applicable regulations and standards.
The ideal candidate will have a strong understanding of global regulations such as 21 CFR 812, IVDR, and MDR, as well as proven expertise with ISO 14155, ISO 20916, and ISO 13485.
Excellent communication and interpersonal skills are essential for this role, as the candidate will need to effectively engage and collaborate with internal and external stakeholders.
