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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.
Requirements
- 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
Tasks
- 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
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- MS Office
- ERP
Benefits
Diverse Work
- Interesting tasks and responsibilities
Informal Culture
- Competent and collegial team
- Flat hierarchies
- Performance-promoting corporate culture
Learning & Development
- Wide array of training
Modern Office
- Modern and attractive workplace
Flexible Working
- Flexible working
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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.
Requirements
- 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
Tasks
- 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
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- MS Office
- ERP
Benefits
Diverse Work
- Interesting tasks and responsibilities
Informal Culture
- Competent and collegial team
- Flat hierarchies
- Performance-promoting corporate culture
Learning & Development
- Wide array of training
Modern Office
- Modern and attractive workplace
Flexible Working
- Flexible working
About the Company
IMCD Group
Industry
Manufacturing
Description
Das Unternehmen ist ein renommiertes, international tätiges und stetig wachsendes Unternehmen.
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