DA
Daiichi Sankyo Europe12 Tage
Head of Bioconjugation Research(m/w/x)
Management
Vollzeit
Keine Angabe
Pfaffenhofen an der Ilm
Nejo KI-Zusammenfassung
In this role, you will spearhead the creation of a new drug substance development unit for Antibody-Drug Conjugates. You will oversee everything from laboratory establishment to team recruitment and GMP production planning, while collaborating across departments to ensure regulatory compliance.
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Anforderungen
- •MSc in Biotechnology or comparable
- •Several years of management experience in biotechnological production
- •Detailed GMP knowledge in biotechnological active ingredient production
- •Strong knowledge of regulatory requirements and hands-on experience in IND/IMPD submissions
- •Solid know-how of technical building requirements and handling of high potent API
- •Experience in managing global project teams
- •Independent and goal-oriented working style, organisational skills, and high level of commitment
- •Very good knowledge of German and English
Master-Abschluss
ODER
Doktor / Ph.D.
Berufserfahrung
ca. 4 – 6 Jahre
Deine Aufgaben
- •Lead the establishment of a new drug substance development unit for Antibody-Drug Conjugates (ADC)
- •Establish a bioconjugation process development laboratory
- •Construct a GMP bioconjugation area in the new biotechnological development building
- •Support construction activities for the GMP production suites
- •Build and lead teams of scientists and operators
- •Manage the newly established bioconjugation area post-project completion
- •Establish and manage the bioconjugation process development laboratory focusing on specific requirements
- •Supervise the implementation of the construction project for GMP production suites
- •Recruit and train scientific development staff and GMP production team
- •Prepare and implement production and resource planning
- •Act as the main technical contact for process-related questions
- •Collaborate with departments such as Antibody production, Quality Management, and Research & Development
- •Organize and release manufacturing instructions in a GMP regulated environment
- •Plan, commission, and control the use of external service providers
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Daiichi Sankyo Europe erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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