Regulatory Affairs Jobs in Tirol
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Suchergebnisse - Regulatory Affairs Jobs in Tirol
Novartis Farmacéutica-Lienz
Regulatory Affairs CMC Associate Director
Job ID REQ-10011560
Sep 02, 2024
Austria
Summary
Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives.
To do this, we are optimizing...
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6 ähnliche Jobs: Innsbruck, Imst, Kitzbühel, Landeck, Kufstein...
Sandoz-Kundl
diploma
• 2 years of experience within Regulatory Affairs for Biosimilars
• User knowledge of MS Office (Word, Excel, Outlook)
• Experience in dealing with databases is an advantage
• Good written and spoken German and English skills
• Structured...
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Healthcare Businesswomen’s Association-Kundl
as needed
• Serve as a strategic partner for internal stakeholders from regulatory affairs, pharmacovigilance, medical, country organizations, and other relevant functions
• Provide labeling input for aggregate reports, Risk Management Plans (RMPs...
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Sandoz-Kundl
for safety related Health Authority requests.
• Liaise with internal stakeholders from regulatory affairs, pharmacovigilance, medical, country organizations and other relevant functions.
• Support audits/inspections on safety label screening...
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Novartis Farmacéutica-Kufstein
in chemistry, biology, pharmacy, biotechnology or equivalent.
• More than 3 years of experience in an operational GxP area, in Manufacturing, Development or QA or Regulatory Affairs; with a thorough knowledge of biologic drug product manufacturing processes...
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6 ähnliche Jobs: Innsbruck, Imst, Lienz, Reutte, Kitzbühel...
Novartis Pharma GmbH-Langkampfen
/Gesundheitswesen/Pharma | Wissenschaft/Forschung
• Job merken
Regulatory Affairs CMC Associate Director
02. 10.2024, Novartis Pharma GmbH
Langkampfen
Medizin/Gesundheitswesen/Pharma | Wissenschaft/Forschung
• Job merken
Regulatory Affairs Medical Device Manager...
myability.jobs -
Sandoz-Kundl
Regulatory Affairs Manager; Biosimilars (d/f/m)
Biosimilars, Kundl, Austria
Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Generic and Biosimilar medicines.
Now as...
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Novartis Pharma GmbH-Langkampfen
Bewerben
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Regulatory Affairs CMC Associate Director
02. 10.2024, Novartis Pharma GmbH
Langkampfen
Medizin/Gesundheitswesen/Pharma | Wissenschaft/Forschung
• Job merken
QA Compliance...
myability.jobs -
Novartis Pharma GmbH-Langkampfen
for clinical trials and commercial production.
• Support Regulatory Affairs to prepare medical device/combination product pre-registration documents and provides input to answer health authority questions.
• Support internal & external audits on...
myability.jobs -
Novartis Pharma GmbH-Langkampfen
Regulatory Affairs CMC Associate Director
Summary
Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people's lives.
To do this, we are optimizing and strengthening our processes and ways of working. We are...
myability.jobs -
Novartis Pharma GmbH-Langkampfen
Wissenschaft/Forschung
• Job merken
Regulatory Affairs CMC Associate Director
02. 10.2024, Novartis Pharma GmbH
Langkampfen
Medizin/Gesundheitswesen/Pharma | Wissenschaft/Forschung
• Job merken
AS&T Expert
24. 10.2024, Novartis Pharma GmbH
Langkampfen...
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Novartis Pharma GmbH-Langkampfen
/Forschung
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Regulatory Affairs CMC Associate Director
02. 10.2024, Novartis Pharma GmbH
Langkampfen
Medizin/Gesundheitswesen/Pharma | Wissenschaft/Forschung
• Job merken
AS&T Expert
24. 10.2024, Novartis Pharma GmbH
Langkampfen
Medizin...
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Novartis Pharma GmbH-Langkampfen
personally and professionally: https://www.novartis.com/careers/benefits-rewards
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Regulatory Affairs CMC Associate Director
02. 10.2024, Novartis Pharma GmbH
Langkampfen...
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Novartis Pharma GmbH-Langkampfen
/Forschung
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Associate Director, Technical Transfer Team - Medical Devices
08. 10.2024, Novartis Pharma GmbH
Langkampfen
Medizin/Gesundheitswesen/Pharma | Wissenschaft/Forschung
• Job merken
Regulatory Affairs Medical Device Manager (Schaftenau...
myability.jobs -
Novartis Pharma GmbH-Langkampfen
Fluent English (German desired).
• More than 3 years of experience in an operational GxP area, in Manufacturing, Development or QA or Regulatory Affairs; with a thorough knowledge of biologic drug product manufacturing processes.
• Ability to speak up...
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