Die KI-Suchmaschine für Jobs
Head of Quality Projects(m/w/x)
Beschreibung
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.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •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)
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •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
Sprachen
english – verhandlungssicher
french – verhandlungssicher
Benefits
Flexibles Arbeiten
- •Flexible work arrangements
- •Remote work possibility
Workation & Sabbatical
- •Opportunities for international work
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Head of Quality Projects(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
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.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •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)
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •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
Sprachen
english – verhandlungssicher
french – verhandlungssicher
Benefits
Flexibles Arbeiten
- •Flexible work arrangements
- •Remote work possibility
Workation & Sabbatical
- •Opportunities for international work
Über das Unternehmen
Adragos Pharma
Branche
Pharmaceuticals
Beschreibung
Adragos Pharma is a reliable Contract Development and Manufacturing Organization (CDMO) providing comprehensive services for drug products.
- Stryker
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