Dein persönlicher KI-Karriere-Agent
Manager, Regulatory Affairs CMC(m/w/x)
Leading global CMC submission activities, authoring high-quality documentation for a global pharmaceutical company. Regulatory CMC or pharmaceutical industry experience expected. On-site childcare facilities.
Anforderungen
- Science degree or equivalent qualification
- Regulatory CMC or pharmaceutical industry experience
- Knowledge of chemistry, analytics, or regulations
- Ability to critically evaluate scientific data
Aufgaben
- Lead global CMC regulatory strategies
- Balance business benefits with compliance
- Manage global CMC submission activities
- Coordinate technical source document delivery
- Author high-quality CMC submission documentation
- Ensure technical congruency and compliance
- Meet e-publishing and timeline requirements
- Communicate regulatory risks to stakeholders
- Represent the department in cross-functional teams
- Prepare CMC risk management assessments
- Lead Health Authority interactions and negotiations
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
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
- Recruitment process adjustments
- Disability representative involvement
Noch nicht perfekt?
- NovartisVollzeitnur vor OrtSeniorSchaftenauab 78.383,9 / 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
QA Compliance Expert – Sampling and Manufacturing(m/w/x)
Vollzeitnur vor OrtBerufserfahrenKundlab 64.023,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Technical Transfer Lead, Medical Device(m/w/x)
Vollzeitnur vor OrtBerufserfahrenSchaftenauab 65.605,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Technical Transfer Lead(m/w/x)
Vollzeit/Teilzeitnur vor OrtBerufserfahrenSchaftenauab 65.605,54 / Jahr
Manager, Regulatory Affairs CMC(m/w/x)
Leading global CMC submission activities, authoring high-quality documentation for a global pharmaceutical company. Regulatory CMC or pharmaceutical industry experience expected. On-site childcare facilities.
Anforderungen
- Science degree or equivalent qualification
- Regulatory CMC or pharmaceutical industry experience
- Knowledge of chemistry, analytics, or regulations
- Ability to critically evaluate scientific data
Aufgaben
- Lead global CMC regulatory strategies
- Balance business benefits with compliance
- Manage global CMC submission activities
- Coordinate technical source document delivery
- Author high-quality CMC submission documentation
- Ensure technical congruency and compliance
- Meet e-publishing and timeline requirements
- Communicate regulatory risks to stakeholders
- Represent the department in cross-functional teams
- Prepare CMC risk management assessments
- Lead Health Authority interactions and negotiations
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
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
- Recruitment process adjustments
- Disability representative involvement
Über das Unternehmen
Novartis
Branche
Pharmaceuticals
Beschreibung
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Noch nicht perfekt?
- Novartis
Associate Director, Regulatory Affairs CMC(m/w/x)
Vollzeitnur vor OrtSeniorSchaftenauab 78.383,9 / 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
QA Compliance Expert – Sampling and Manufacturing(m/w/x)
Vollzeitnur vor OrtBerufserfahrenKundlab 64.023,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Technical Transfer Lead, Medical Device(m/w/x)
Vollzeitnur vor OrtBerufserfahrenSchaftenauab 65.605,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Technical Transfer Lead(m/w/x)
Vollzeit/Teilzeitnur vor OrtBerufserfahrenSchaftenauab 65.605,54 / Jahr