Clinical Trials Jobs in Tirol
1 - 7 von 7
Suchergebnisse - Clinical Trials Jobs in Tirol
Daiichi Sankyo-Pfaffenhofen
Alle Tätigkeiten, die der Rolle einer Sachkundigen Person nach § 14 AMG für klinische Prüfpräparate, EU-GMP Guide Annex 16, Annex 13 und Clinical Trial Regulation (CTR) für klinische Prüfpräparate entsprechen.
• Entscheidung über Freigabe bzw. Zurückweisung...
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Novartis Pharma GmbH-Langkampfen
clinical trial and investigating the stability behavior of the drugs. Furthermore, we are validating the methods used for release and will be also responsible for transferring the methods to our commercial organization or external partners.
The role...
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Healthcare Businesswomen’s Association-Lienz
IT validations, etc.
• Review and approve quality deliverables to ensure compliance (including procedures, records, third party work, contractors, clinical trial material, components, gap assessments )
• Reporting of technical complaints / adverse...
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6 ähnliche Jobs: Kufstein, Kitzbühel, Reutte, Imst, Innsbruck...
Novartis Pharma GmbH-Langkampfen
Senior Expert - Analytical Operations (m/f/d)
Summary
About the role: #LI-Hybrid
As a Senior Expert you will be part of a team developing new Biologic drugs. Analytical Operations is the team releasing the product for clinical trial...
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Novartis Farmacéutica-Innsbruck
the product for clinical trial and investigating the stability behavior of the drugs. Furthermore, we are validating the methods used for release and will be also responsible for transferring the methods to our commercial organization or external...
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appcast.io -
6 ähnliche Jobs: Imst, Kufstein, Kitzbühel, Reutte, Landeck...
Novartis Pharma GmbH-Langkampfen
plans, training, IT validations, etc.
• Review and approve quality deliverables to ensure compliance (including procedures, records, third party work, contractors, clinical trial material, components, gap assessments )
• Reporting of technical complaints...
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myability.jobs -
Novartis Pharma GmbH-Langkampfen
and strategic risks
• Supporting and/or preparing high quality dossiers, drug substance and/or drug product quality documentation to support global regulatory submissions (e.g. Clinical Trial Applications, Market Authorization Applications, post-approval...
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