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Technical Support Manager API(m/w/x)
Central contact for API manufacturers in pharmaceutical supply chain, managing EMEA regulatory and quality needs. Regulatory Affairs experience (API focus) and GMP/GDP knowledge essential. Autonomous work, international environment.
Anforderungen
- Education in Chemistry, Pharmacy, Veterinary or Biology
- Experience in Regulatory Affairs (preferably API-perspective)
- Knowledge of Quality Assurance (GMP or GDP)
- Knowledge of Swiss medicinal product regulations (preferably)
- Teamwork, autonomy, and strong organizational skills
- Communicative, convincing personality and structured working
- Good knowledge of MS Office and ERP
- Fluency in English and German
Aufgaben
- Address EMEA regulatory and quality needs
- Act as central contact for manufacturers
- Implement strategic pharmaceutical business goals
- Build networks with regulatory and quality teams
- Process and prioritize technical requests autonomously
- Assist customers with API registrations
- Lead investigations into non-conformities and returns
- Negotiate quality agreements and CDAs
- Coordinate and attend GDP and GMP audits
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- MS Office
- ERP
Benefits
Abwechslungsreiche Aufgaben
- Interesting tasks and responsibilities
Lockere Unternehmenskultur
- Competent and collegial team
- Flat hierarchies
- Performance-promoting corporate culture
Weiterbildungsangebote
- Wide array of training
Modernes Büro
- Modern and attractive workplace
Flexibles Arbeiten
- Flexible working
Noch nicht perfekt?
- IMCD GroupVollzeitnur vor OrtBerufserfahrenSachseln
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Technical Support Manager API(m/w/x)
Central contact for API manufacturers in pharmaceutical supply chain, managing EMEA regulatory and quality needs. Regulatory Affairs experience (API focus) and GMP/GDP knowledge essential. Autonomous work, international environment.
Anforderungen
- Education in Chemistry, Pharmacy, Veterinary or Biology
- Experience in Regulatory Affairs (preferably API-perspective)
- Knowledge of Quality Assurance (GMP or GDP)
- Knowledge of Swiss medicinal product regulations (preferably)
- Teamwork, autonomy, and strong organizational skills
- Communicative, convincing personality and structured working
- Good knowledge of MS Office and ERP
- Fluency in English and German
Aufgaben
- Address EMEA regulatory and quality needs
- Act as central contact for manufacturers
- Implement strategic pharmaceutical business goals
- Build networks with regulatory and quality teams
- Process and prioritize technical requests autonomously
- Assist customers with API registrations
- Lead investigations into non-conformities and returns
- Negotiate quality agreements and CDAs
- Coordinate and attend GDP and GMP audits
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- MS Office
- ERP
Benefits
Abwechslungsreiche Aufgaben
- Interesting tasks and responsibilities
Lockere Unternehmenskultur
- Competent and collegial team
- Flat hierarchies
- Performance-promoting corporate culture
Weiterbildungsangebote
- Wide array of training
Modernes Büro
- Modern and attractive workplace
Flexibles Arbeiten
- Flexible working
Über das Unternehmen
IMCD Group
Branche
Manufacturing
Beschreibung
Das Unternehmen ist ein renommiertes, international tätiges und stetig wachsendes Unternehmen.
Noch nicht perfekt?
- IMCD Group
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Vollzeitnur vor OrtBerufserfahrenOberdorf (NW)