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Head of Quality Projects(m/w/x)
Description
In this role, you will lead quality initiatives for new products and manufacturing capabilities, ensuring compliance in a GMP environment while driving continuous improvement and fostering teamwork across projects.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •University degree (master’s level or equivalent) in pharmaceutical sciences, chemical engineering, biology, or a related field
- •Solid expertise in manufacturing systems, process development, facilities, equipment, and utilities
- •In-depth knowledge of aseptic processing and technology/product transfers
- •Strong understanding of regulatory requirements: US FDA, EMA, Swissmedic
- •Proven leadership experience in quality assurance
- •Advanced analytical skills, data-driven, with a focus on continuous improvement
- •Excellent cross-functional teamworking & communication skills
- •Comfortable working in a demanding international environment
- •Fluent in French and English (spoken and written)
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Provide quality and technical leadership for key manufacturing projects
- •Support the evaluation and introduction of new products and processes
- •Represent quality in cross-functional projects within a GMP-regulated environment
- •Implement enhancements, metrics, and KPIs to optimize processes
- •Coordinate QA, QC, and validation support for major projects
- •Contribute to continuous improvement and performance enhancement
- •Promote collaborative leadership and teamwork on-site and across multi-site projects
Languages
english – Business Fluent
french – Business Fluent
Benefits
Flexible Working
- •Flexible work arrangements
- •Remote work possibility
Workation & Sabbatical
- •Opportunities for international work
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Head of Quality Projects(m/w/x)
The AI Job Search Engine
Description
In this role, you will lead quality initiatives for new products and manufacturing capabilities, ensuring compliance in a GMP environment while driving continuous improvement and fostering teamwork across projects.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •University degree (master’s level or equivalent) in pharmaceutical sciences, chemical engineering, biology, or a related field
- •Solid expertise in manufacturing systems, process development, facilities, equipment, and utilities
- •In-depth knowledge of aseptic processing and technology/product transfers
- •Strong understanding of regulatory requirements: US FDA, EMA, Swissmedic
- •Proven leadership experience in quality assurance
- •Advanced analytical skills, data-driven, with a focus on continuous improvement
- •Excellent cross-functional teamworking & communication skills
- •Comfortable working in a demanding international environment
- •Fluent in French and English (spoken and written)
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Provide quality and technical leadership for key manufacturing projects
- •Support the evaluation and introduction of new products and processes
- •Represent quality in cross-functional projects within a GMP-regulated environment
- •Implement enhancements, metrics, and KPIs to optimize processes
- •Coordinate QA, QC, and validation support for major projects
- •Contribute to continuous improvement and performance enhancement
- •Promote collaborative leadership and teamwork on-site and across multi-site projects
Languages
english – Business Fluent
french – Business Fluent
Benefits
Flexible Working
- •Flexible work arrangements
- •Remote work possibility
Workation & Sabbatical
- •Opportunities for international work
About the Company
Adragos Pharma
Industry
Pharmaceuticals
Description
Adragos Pharma is a reliable Contract Development and Manufacturing Organization (CDMO) providing comprehensive services for drug products.
- Stryker
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