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Certifying batches of medical products for a Swiss pharma company, ensuring GMP and Marketing Authorization compliance. Recognized QP status and fluent German/English required. Flexible hours, home office option, international environment.
Requirements
- University degree in Pharmacy, Chemistry, or life sciences
- Recognized QP status and valid health authority authorization
- Proven pharmaceutical industry and pharmacovigilance experience (GVP)
- Fluent German and English communication skills
- Strong understanding of regulatory requirements and quality standards
- Strong computer literacy and familiarity with digital QMS and LIMS
- Ability to drive change and foster quality culture
Tasks
- Certify batches of medical products
- Ensure compliance with Marketing Authorization and GMP
- Oversee batch release activities
- Investigate and document deviations and CAPAs
- Prevent distribution of non-compliant or falsified medicines
- Ensure third-party manufacturers comply with GMP
- Maintain current knowledge of legal and technical standards
- Certify and release medicinal product batches
- Contribute to quality team efforts
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- digital QMS
- LIMS
Benefits
Flexible Working
- Flexible working hours
- Home office possibility
Informal Culture
- International working environment
- Motivated, agile and service-oriented team
Startup Environment
- Growing company
Other Benefits
- Quality and customer-oriented environment
Diverse Work
- Interesting and highly diversified tasks
Career Advancement
- Broad career basis in pharmaceutical industry
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Certifying batches of medical products for a Swiss pharma company, ensuring GMP and Marketing Authorization compliance. Recognized QP status and fluent German/English required. Flexible hours, home office option, international environment.
Requirements
- University degree in Pharmacy, Chemistry, or life sciences
- Recognized QP status and valid health authority authorization
- Proven pharmaceutical industry and pharmacovigilance experience (GVP)
- Fluent German and English communication skills
- Strong understanding of regulatory requirements and quality standards
- Strong computer literacy and familiarity with digital QMS and LIMS
- Ability to drive change and foster quality culture
Tasks
- Certify batches of medical products
- Ensure compliance with Marketing Authorization and GMP
- Oversee batch release activities
- Investigate and document deviations and CAPAs
- Prevent distribution of non-compliant or falsified medicines
- Ensure third-party manufacturers comply with GMP
- Maintain current knowledge of legal and technical standards
- Certify and release medicinal product batches
- Contribute to quality team efforts
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- digital QMS
- LIMS
Benefits
Flexible Working
- Flexible working hours
- Home office possibility
Informal Culture
- International working environment
- Motivated, agile and service-oriented team
Startup Environment
- Growing company
Other Benefits
- Quality and customer-oriented environment
Diverse Work
- Interesting and highly diversified tasks
Career Advancement
- Broad career basis in pharmaceutical industry
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Acino
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein Schweizer Pharmaunternehmen, führend in fortschrittlichen Technologien zur Verabreichung von Medikamenten.
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