Drug Regulatory Affairs Jobs
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Suchergebnisse - Drug Regulatory Affairs Jobs
Healthcare Businesswomen’s Association-Kundl
Job Description Summary
Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Generic and Biosimilar medicines.
As a member of our Regulatory Affairs Drug Substance team, your role...
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Novartis Farmacéutica-Reutte
Combination Products regulatory affairs experience, in the pharmaceutical and/or medical device industry.
• Good knowledge and experience in medical device & Drug/Device Combination Products regulatory submissions and approval processes, with understanding of...
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Novartis-Langkampfen
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 and to take Quality decisions during...
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Novartis Farmacéutica-Lienz
development and post-approval activities. You bring a foundation of regulatory knowledge regarding drug development, manufacturing, and analytical testing, as well as a collaborative and patient-focused mindset.
We are seeking key talent, like you, to join us...
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Novartis Pharma GmbH-Langkampfen
bring regulatory knowledge regarding drug development, manufacturing, and analytical testing, as well as a collaborative and patient-focused mindset.
About the Role
Major accountabilities:
• Formulate and lead global CMC regulatory strategy with a...
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Healthcare Businesswomen’s Association-Kundl
Ensures rapid and timely approval of new drugs, biologics/biotechnology and/or medical devices and continued approved status of marketed drugs or medical devices. Serves as regulatory representative to marketing or research project teams and government...
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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
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Regulatory Affairs Medical Device Manager (Schaftenau...
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Advanced Accelerator Applications (Italy) - S...-Österreich
degree 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...
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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-Österreich
More than 3 years of experience in an operational Gx P area, in Manufacturing, Development or QA or Regulatory Affairs; with a thorough knowledge of biologic drug product manufacturing processes.
• Ability to speak up and to take Quality decisions...
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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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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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Novartis Pharma GmbH-Langkampfen
/Pharma | Technik/Ingenieurwesen
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Regulatory Affairs CMC Associate Director
02. 10.2024, Novartis Pharma GmbH
Langkampfen
Medizin/Gesundheitswesen/Pharma | Wissenschaft/Forschung
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SCM Sourcing Officer
24. 09.2024, Novartis Pharma GmbH...
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Sandoz International GmbH-Österreich
information on a product.
4. Act as Subject Matter Expert (SME) for safety related Health Authority requests.
5. Liaise with internal stakeholders from regulatory affairs, pharmacovigilance, medical, country organizations and other relevant functions.
6. ..
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Sandoz International GmbH-Österreich
as needed
4. Serve as a strategic partner for internal stakeholders from regulatory affairs, pharmacovigilance, medical, country organizations, and other relevant functions
5. Provide labeling input for aggregate reports, Risk Management Plans (RMPs...
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