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Technical Support Manager API(m/w/x)
Description
You will drive the company's global pharmaceutical business by bridging the gap between regional regulatory needs and manufacturer quality standards through expert technical support.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
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
Tools & Technologies
Languages
English – Business Fluent
German – Business Fluent
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)
The AI Job Search Engine
Description
You will drive the company's global pharmaceutical business by bridging the gap between regional regulatory needs and manufacturer quality standards through expert technical support.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
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
Tools & Technologies
Languages
English – Business Fluent
German – Business Fluent
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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