Lonza
Senior QA Specialist, QA Operations(m/w/x)
Vollzeitnur vor OrtSenior
Visp
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
LOLonza
Senior QA Specialist – Infrastructure and Logistics(m/w/x)
Visp
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Ensuring GMP compliance for shared utility and logistics systems at a global pharmaceutical manufacturer. Academic degree and pharmaceutical QA experience required. Relocation assistance provided.
Anforderungen
- Academic degree in Pharmaceutical Sciences, Biochemistry, Engineering, Chemistry, or related field
- Work experience in Quality Assurance, Production/Supply Chain/Engineering, or Quality Control in pharmaceutical industries and cGMP-controlled environments
- Knowledge of Swiss, EU, and US GMP regulations for audits/inspections and compliance systems
- Strong verbal and written communication skills in English (German advantageous)
- Ability to communicate quality and compliance requirements to varying organizational levels
- Strong collaborative mindset and ability to build relationships quickly
- Strong organizational skills and ability to balance multiple priorities
- Problem-solving ability, understanding details and strategic picture, providing practical solutions
Aufgaben
- Implement and manage cross-functional support for facilities
- Assure Quality Assurance of sites and facilities
- Ensure shared utility systems meet standards
- Ensure logistics areas meet standards
- Provide QA support for GMP & Compliance
- Provide QA support for Cold-chain
- Provide QA support for supply chain
- Provide QA support for good warehousing practice
- Provide QA support for Clean utilities
- Provide QA oversight for shared utility systems
- Provide QA oversight for logistics areas
- Organize Deviation Review Boards
- Lead Deviation Review Boards
- Review Change Requests
- Assess Change Requests
- Review Corrective and Preventative Actions (CAPA)
- Assess Corrective and Preventative Actions (CAPA)
- Approve standard operation procedures for utilities
- Approve standard operation procedures for logistics
- Review GMP impact of utility alarms
- Review GMP impact of cold-chain alarms
- Review GMP impact of utility incidents
- Review GMP impact of cold-chain incidents
- Assist with operational readiness activities
- Assess risks in relevant areas
- Support internal audits
- Support external audits
- Support inspections
- Represent Quality at meetings
- Lead local implementation of global Quality policies
- Support local implementation of global Quality policies
- Lead local implementation of global Quality standards
- Support local implementation of global Quality standards
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – Grundkenntnisse
Tools & Technologien
- cGMP
Benefits
Mitarbeiterrabatte
- Lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Sonstige Vorteile
- Relocation assistance
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Lonza erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- Lonza
Senior QA Specialist - Qualification/Validation/EM (Environmental Monitoring)(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
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Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist, DPS (Drug Product Services)(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp
LOLonza
Senior QA Specialist – Infrastructure and Logistics(m/w/x)
Visp
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Ensuring GMP compliance for shared utility and logistics systems at a global pharmaceutical manufacturer. Academic degree and pharmaceutical QA experience required. Relocation assistance provided.
Anforderungen
- Academic degree in Pharmaceutical Sciences, Biochemistry, Engineering, Chemistry, or related field
- Work experience in Quality Assurance, Production/Supply Chain/Engineering, or Quality Control in pharmaceutical industries and cGMP-controlled environments
- Knowledge of Swiss, EU, and US GMP regulations for audits/inspections and compliance systems
- Strong verbal and written communication skills in English (German advantageous)
- Ability to communicate quality and compliance requirements to varying organizational levels
- Strong collaborative mindset and ability to build relationships quickly
- Strong organizational skills and ability to balance multiple priorities
- Problem-solving ability, understanding details and strategic picture, providing practical solutions
Aufgaben
- Implement and manage cross-functional support for facilities
- Assure Quality Assurance of sites and facilities
- Ensure shared utility systems meet standards
- Ensure logistics areas meet standards
- Provide QA support for GMP & Compliance
- Provide QA support for Cold-chain
- Provide QA support for supply chain
- Provide QA support for good warehousing practice
- Provide QA support for Clean utilities
- Provide QA oversight for shared utility systems
- Provide QA oversight for logistics areas
- Organize Deviation Review Boards
- Lead Deviation Review Boards
- Review Change Requests
- Assess Change Requests
- Review Corrective and Preventative Actions (CAPA)
- Assess Corrective and Preventative Actions (CAPA)
- Approve standard operation procedures for utilities
- Approve standard operation procedures for logistics
- Review GMP impact of utility alarms
- Review GMP impact of cold-chain alarms
- Review GMP impact of utility incidents
- Review GMP impact of cold-chain incidents
- Assist with operational readiness activities
- Assess risks in relevant areas
- Support internal audits
- Support external audits
- Support inspections
- Represent Quality at meetings
- Lead local implementation of global Quality policies
- Support local implementation of global Quality policies
- Lead local implementation of global Quality standards
- Support local implementation of global Quality standards
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – Grundkenntnisse
Tools & Technologien
- cGMP
Benefits
Mitarbeiterrabatte
- Lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Sonstige Vorteile
- Relocation assistance
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Lonza erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
Lonza
Branche
Pharmaceuticals
Beschreibung
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Noch nicht perfekt?
- Lonza
Senior QA Specialist, QA Operations(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist - Qualification/Validation/EM (Environmental Monitoring)(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist, DPS (Drug Product Services)(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp