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Manufacturing Manager Operations USP(m/w/x)
Overseeing production of commercial, clinical, and toxicology supplies at a global life sciences firm, leading a 10-person technical team. GMP compliance experience and team leadership background required. Regular interaction with customers and regulatory auditors.
Anforderungen
- Bachelor's degree or higher
- Experience in Manufacturing or related fields
- Background in team management
- Maturity, confidence, and emotional intelligence
- Agile relationship management skills
- Fluent English and German
Aufgaben
- Manufacture commercial, clinical, and toxicology supplies
- Ensure compliance with GMP regulations
- Lead a technical team of ten contributors
- Coach and train employees to improve performance
- Interface with customers and regulatory auditors
- Lead facility tours for auditors
- Remediate all audit observations
- Allocate resources to achieve production goals
- Review and approve QMS investigations
- Manage production schedules with customers
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- GMP
Noch nicht perfekt?
- CH12 Lonza AGVollzeitnur vor OrtManagementVisp
- Lonza
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Bioprocess Engineer in USP / DSP / BioConjugates(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Teamlead Operations(m/w/x)
Vollzeitnur vor OrtManagementVisp
Manufacturing Manager Operations USP(m/w/x)
Overseeing production of commercial, clinical, and toxicology supplies at a global life sciences firm, leading a 10-person technical team. GMP compliance experience and team leadership background required. Regular interaction with customers and regulatory auditors.
Anforderungen
- Bachelor's degree or higher
- Experience in Manufacturing or related fields
- Background in team management
- Maturity, confidence, and emotional intelligence
- Agile relationship management skills
- Fluent English and German
Aufgaben
- Manufacture commercial, clinical, and toxicology supplies
- Ensure compliance with GMP regulations
- Lead a technical team of ten contributors
- Coach and train employees to improve performance
- Interface with customers and regulatory auditors
- Lead facility tours for auditors
- Remediate all audit observations
- Allocate resources to achieve production goals
- Review and approve QMS investigations
- Manage production schedules with customers
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- GMP
Über das Unternehmen
Lonza
Branche
Pharmaceuticals
Beschreibung
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Noch nicht perfekt?
- CH12 Lonza AG
Manager Manufacturing(m/w/x)
Vollzeitnur vor OrtManagementVisp - Lonza
Bioprocess Engineer Large Scale Mammalian USP(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Bioprocess Engineer Mammalian (USP/DSP)(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Bioprocess Engineer in USP / DSP / BioConjugates(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Teamlead Operations(m/w/x)
Vollzeitnur vor OrtManagementVisp