Die KI-Suchmaschine für Jobs
Senior Manager GRA CMC Small Molecules Development(m/w/x)
Beschreibung
You will drive global CMC strategies for innovative drug developments, bridging the gap between technical experts and regulatory bodies to ensure life-changing medicines reach patients worldwide.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Degree in pharmacy, chemistry, life science, or Ph.D.
- •Experience in pharmaceutical industry, Health Authorities, or CMC
- •Experience with NCEs or drug-linkers for ADCs
- •Knowledge of global regulatory CMC requirements
- •Experience driving CMC activities and authoring dossiers
- •Excellent written and spoken English skills
- •Passion for team collaboration and problem-solving
Ausbildung
Berufserfahrung
5 Jahre
Aufgaben
- •Lead global regulatory CMC activities for clinical phases and launches
- •Develop global regulatory CMC and dossier strategies
- •Liaise between Global Regulatory Affairs and technical functions
- •Author and approve regulatory quality documents like MAA and IND
- •Translate country-specific regulations into technical requirements
- •Advise technical experts on analytical and drug development
- •Provide strategic CMC guidance to global regulatory functions
- •Participate in interdisciplinary CMC and regulatory project teams
- •Lead Health Authority interactions and meetings
- •Perform expert CMC assessments for licensing and due diligence
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- •Hybrid work format
- •Remote work possible
Karriere- und Weiterentwicklung
- •Access and growth opportunities
Sonstige Vorteile
- •Workplace accessibility accommodations
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Jobs in der Nähe entdecken
Senior Manager GRA CMC Small Molecules Development(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
You will drive global CMC strategies for innovative drug developments, bridging the gap between technical experts and regulatory bodies to ensure life-changing medicines reach patients worldwide.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Degree in pharmacy, chemistry, life science, or Ph.D.
- •Experience in pharmaceutical industry, Health Authorities, or CMC
- •Experience with NCEs or drug-linkers for ADCs
- •Knowledge of global regulatory CMC requirements
- •Experience driving CMC activities and authoring dossiers
- •Excellent written and spoken English skills
- •Passion for team collaboration and problem-solving
Ausbildung
Berufserfahrung
5 Jahre
Aufgaben
- •Lead global regulatory CMC activities for clinical phases and launches
- •Develop global regulatory CMC and dossier strategies
- •Liaise between Global Regulatory Affairs and technical functions
- •Author and approve regulatory quality documents like MAA and IND
- •Translate country-specific regulations into technical requirements
- •Advise technical experts on analytical and drug development
- •Provide strategic CMC guidance to global regulatory functions
- •Participate in interdisciplinary CMC and regulatory project teams
- •Lead Health Authority interactions and meetings
- •Perform expert CMC assessments for licensing and due diligence
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- •Hybrid work format
- •Remote work possible
Karriere- und Weiterentwicklung
- •Access and growth opportunities
Sonstige Vorteile
- •Workplace accessibility accommodations
Über das Unternehmen
SUSONITY
Branche
Healthcare
Beschreibung
Das Unternehmen entwickelt Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit.
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