Dein persönlicher KI-Karriere-Agent
Regulatory Affairs Associate Director, CMC(m/w/x)
Global CMC regulatory strategy development and submission coordination. Strong CMC regulatory understanding and scientific data evaluation skills required. Childcare facilities, learning and development options.
Anforderungen
- English fluency (written and spoken)
- Scientific degree or equivalent experience
- CMC Regulatory Affairs capability
- Strong CMC regulatory understanding
- Scientific data evaluation skills
- Pharmaceutical development knowledge
- Cross-functional team collaboration
- Planning and organisational skills
Aufgaben
- Develop and implement global CMC regulatory strategies
- Support regulatory activities across development and lifecycle stages
- Plan and coordinate CMC submission activities
- Author and review CMC regulatory documentation
- Manage alignment on content, quality, and timelines
- Communicate regulatory risks and updates to project teams
- Prepare and support Health Authority interactions
- Collaborate across functions for consistent delivery
- Contribute to continuous improvement initiatives
- Support knowledge sharing within the regulatory community
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
Benefits
Attraktive Vergütung
- Market-competitive base salary
Boni & Prämien
- Attractive incentive program
Betriebliche Altersvorsorge
- Modern company pension scheme
Kinderbetreuung
- Childcare facilities
Weiterbildungsangebote
- Learning and development options
Karriere- und Weiterentwicklung
- Worldwide career opportunities
Sonstige Vorteile
- Support for applicants with disabilities
Abwechslungsreiche Aufgaben
- Advice on suitable positions
Mentoring & Coaching
- Guidance at all stages of application process
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
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Regulatory Affairs Associate Director, CMC(m/w/x)
Global CMC regulatory strategy development and submission coordination. Strong CMC regulatory understanding and scientific data evaluation skills required. Childcare facilities, learning and development options.
Anforderungen
- English fluency (written and spoken)
- Scientific degree or equivalent experience
- CMC Regulatory Affairs capability
- Strong CMC regulatory understanding
- Scientific data evaluation skills
- Pharmaceutical development knowledge
- Cross-functional team collaboration
- Planning and organisational skills
Aufgaben
- Develop and implement global CMC regulatory strategies
- Support regulatory activities across development and lifecycle stages
- Plan and coordinate CMC submission activities
- Author and review CMC regulatory documentation
- Manage alignment on content, quality, and timelines
- Communicate regulatory risks and updates to project teams
- Prepare and support Health Authority interactions
- Collaborate across functions for consistent delivery
- Contribute to continuous improvement initiatives
- Support knowledge sharing within the regulatory community
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
Benefits
Attraktive Vergütung
- Market-competitive base salary
Boni & Prämien
- Attractive incentive program
Betriebliche Altersvorsorge
- Modern company pension scheme
Kinderbetreuung
- Childcare facilities
Weiterbildungsangebote
- Learning and development options
Karriere- und Weiterentwicklung
- Worldwide career opportunities
Sonstige Vorteile
- Support for applicants with disabilities
Abwechslungsreiche Aufgaben
- Advice on suitable positions
Mentoring & Coaching
- Guidance at all stages of application process
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Novartis Pharmaceutical Manufacturing GmbH
Branche
Pharmaceuticals
Beschreibung
The company aims to reimagine medicine to improve and extend people’s lives.
Noch nicht perfekt?
- Novartis
Associate Director, Regulatory Affairs CMC(m/w/x)
Vollzeitnur vor OrtSeniorSchaftenauab 78.383,9 / Jahr - Novartis
Manager, Regulatory Affairs CMC(m/w/x)
Vollzeitnur vor OrtManagementSchaftenauab 65.605,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Drug Product Project Leader – Associate Director Science & Technology(m/w/x)
Vollzeit/Teilzeitnur vor OrtSeniorSchaftenauab 78.383,9 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Technical Transfer Lead(m/w/x)
Vollzeit/Teilzeitnur vor OrtBerufserfahrenSchaftenauab 65.605,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
R&D Quality Lead(m/w/x)
Vollzeitnur vor OrtBerufserfahrenSchaftenauab 78.383,9 / Jahr