BioNTech SE
Director Manufacturing Sciences & Technology(m/w/x)
Vollzeitnur vor OrtSenior
Mainz
Neuer Job?Nejo!
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BOBoehringer Ingelheim
Senior Commercial Process Manager(m/w/x)
Ingelheim am Rhein, Biberach
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Shaping commercial manufacturing processes for innovative pharmaceuticals, including product launches and lifecycle support. Extensive pharmaceutical industry experience, including API manufacturing under cGMP, required. Support for product lifecycle management and interdisciplinary team leadership.
Anforderungen
- University degree with PhD in chemistry or related field
- Extensive experience in pharmaceutical industry (Operations, Regulatory Affairs, Drug Substance Development)
- Proven ability to lead cross-functional matrix teams internationally
- Strong project management expertise
- Practical experience in API manufacturing under cGMP conditions
- Practical experience in GMP process development
- Experience in solid-phase peptide synthesis is an advantage
- Experience in preparative HPLC is an advantage
- Experience in solid-phase oligonucleotide synthesis is an advantage
- Experience in ADCs is an advantage
- Strong regulatory and compliance expertise
- Team-oriented mindset
- Strategic thinking
- High level of commitment
- Flexibility
- Willingness to travel for business
- Very good command of English, written and spoken
- Several years of experience in international business environment
- Applications from persons with severe disabilities warmly welcomed
- Preferential consideration for severely disabled applicants in case of equal qualifications
Aufgaben
- Shape efficient commercial manufacturing processes
- Drive transfer of innovative pharmaceutical products
- Support products throughout their lifecycle
- Lead interdisciplinary project teams
- Prepare and execute product launches
- Manage technology transfers between sites
- Ensure manufacturing process compliance and change management
- Represent Drug Substance function in development departments
- Contribute to strategic initiatives for future improvements
- Ensure stable, cost-efficient, registration-compliant supply
- Maintain GMP-compliant supply to global markets
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- cGMP
- GMP
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Boehringer Ingelheim 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.
Noch nicht perfekt?
- BioNTech SE
Senior Director Protein Modality Lead(m/w/x)
Vollzeitnur vor OrtSeniorMainz - BioNTech SE
Director Process Engineering(m/w/x)
Vollzeitnur vor OrtSeniorMainz - Midas Pharma
Corporate Business Development & Licensing Manager(m/w/x)
Vollzeitnur vor OrtSeniorIngelheim am Rhein - Boehringer Ingelheim
Senior Regulatory Affairs Manager CMC for NCE(m/w/x)
Vollzeitnur vor OrtSeniorBiberach, Ingelheim am Rhein
BOBoehringer Ingelheim
Senior Commercial Process Manager(m/w/x)
Ingelheim am Rhein, Biberach
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Shaping commercial manufacturing processes for innovative pharmaceuticals, including product launches and lifecycle support. Extensive pharmaceutical industry experience, including API manufacturing under cGMP, required. Support for product lifecycle management and interdisciplinary team leadership.
Anforderungen
- University degree with PhD in chemistry or related field
- Extensive experience in pharmaceutical industry (Operations, Regulatory Affairs, Drug Substance Development)
- Proven ability to lead cross-functional matrix teams internationally
- Strong project management expertise
- Practical experience in API manufacturing under cGMP conditions
- Practical experience in GMP process development
- Experience in solid-phase peptide synthesis is an advantage
- Experience in preparative HPLC is an advantage
- Experience in solid-phase oligonucleotide synthesis is an advantage
- Experience in ADCs is an advantage
- Strong regulatory and compliance expertise
- Team-oriented mindset
- Strategic thinking
- High level of commitment
- Flexibility
- Willingness to travel for business
- Very good command of English, written and spoken
- Several years of experience in international business environment
- Applications from persons with severe disabilities warmly welcomed
- Preferential consideration for severely disabled applicants in case of equal qualifications
Aufgaben
- Shape efficient commercial manufacturing processes
- Drive transfer of innovative pharmaceutical products
- Support products throughout their lifecycle
- Lead interdisciplinary project teams
- Prepare and execute product launches
- Manage technology transfers between sites
- Ensure manufacturing process compliance and change management
- Represent Drug Substance function in development departments
- Contribute to strategic initiatives for future improvements
- Ensure stable, cost-efficient, registration-compliant supply
- Maintain GMP-compliant supply to global markets
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- cGMP
- GMP
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Boehringer Ingelheim 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.
Über das Unternehmen
Boehringer Ingelheim
Branche
Pharmaceuticals
Beschreibung
The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.
Noch nicht perfekt?
- BioNTech SE
Director Manufacturing Sciences & Technology(m/w/x)
Vollzeitnur vor OrtSeniorMainz - BioNTech SE
Senior Director Protein Modality Lead(m/w/x)
Vollzeitnur vor OrtSeniorMainz - BioNTech SE
Director Process Engineering(m/w/x)
Vollzeitnur vor OrtSeniorMainz - Midas Pharma
Corporate Business Development & Licensing Manager(m/w/x)
Vollzeitnur vor OrtSeniorIngelheim am Rhein - Boehringer Ingelheim
Senior Regulatory Affairs Manager CMC for NCE(m/w/x)
Vollzeitnur vor OrtSeniorBiberach, Ingelheim am Rhein