CH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Vollzeitnur vor OrtSenior
Visp
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CHCH12 Lonza AG
Associate Director Operation Readiness Lead(m/w/x)
Visp
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Leading operational readiness for project execution and facility readiness in pharmaceutical engineering. Proven GEP/GMP and CQV project management experience required. Global project scope, managing internal and external resources.
Anforderungen
- Master's degree or equivalent experience in Pharma, Engineering, or Science
- Proven experience in Pharma/Engineering (GEP/GMP) with understanding of Small Molecules, Infrastructure, and Laboratories business
- Proven experience in Project Management, CQV
- Understanding of Pharmaceutical/Bio Science 'Contract Manufacturing' business and experience in cGM
- Strong leadership skills with global interaction capability
- Possess financial and commercial acumen linked to project goals, costs & scheduling, and risk
- Strong analytical skills for in-depth analysis of complex/large datasets
- Ability to develop and implement new and standard processes, tools/methodologies in a global context
- Fluency in German and English or willingness to learn one of the two languages
Aufgaben
- Oversee resource allocation, cost estimation, and timeline projection for operational readiness
- Ensure timely completion of tasks with team members and resources
- Highlight and communicate schedule targets, resolve issues, and escalate when necessary
- Manage staffing relevant to operations for project execution and facility readiness
- Identify and lead internal or external resources for project execution
- Provide inputs and monitor the Project Execution Plan and Project Quality Plan
- Supervise implemented commissioning, qualification, and validation strategies
- Lead Startup and CQV activities to ensure compliance with regulations and standards
- Oversee project plans for timely completion of CQV, post OQ, and startup deliverables
- Collaborate with cross-functional teams to identify and mitigate CAPEX investment risks
- Develop and maintain relationships with key stakeholders for successful project execution
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Boni & Prämien
- Compensation programs that recognize high performance
Sonstige Vorteile
- Lifestyle benefits
- Relocation assistance
Familienfreundlichkeit
- Family benefits
Mitarbeiterrabatte
- Leisure benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
- Inclusive workplace
Sinnstiftende Arbeit
- Ethical workplace
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens CH12 Lonza AG 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?
- CH12 Lonza AG
Associate Director, Quality Strategy and Operations(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
Qualification CQV Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
Associate Director, QA SAP Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Head of CQV/CSV - Advanced Synthesis Conjugates(m/w/x)
Vollzeitnur vor OrtSeniorVisp
CHCH12 Lonza AG
Associate Director Operation Readiness Lead(m/w/x)
Visp
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Leading operational readiness for project execution and facility readiness in pharmaceutical engineering. Proven GEP/GMP and CQV project management experience required. Global project scope, managing internal and external resources.
Anforderungen
- Master's degree or equivalent experience in Pharma, Engineering, or Science
- Proven experience in Pharma/Engineering (GEP/GMP) with understanding of Small Molecules, Infrastructure, and Laboratories business
- Proven experience in Project Management, CQV
- Understanding of Pharmaceutical/Bio Science 'Contract Manufacturing' business and experience in cGM
- Strong leadership skills with global interaction capability
- Possess financial and commercial acumen linked to project goals, costs & scheduling, and risk
- Strong analytical skills for in-depth analysis of complex/large datasets
- Ability to develop and implement new and standard processes, tools/methodologies in a global context
- Fluency in German and English or willingness to learn one of the two languages
Aufgaben
- Oversee resource allocation, cost estimation, and timeline projection for operational readiness
- Ensure timely completion of tasks with team members and resources
- Highlight and communicate schedule targets, resolve issues, and escalate when necessary
- Manage staffing relevant to operations for project execution and facility readiness
- Identify and lead internal or external resources for project execution
- Provide inputs and monitor the Project Execution Plan and Project Quality Plan
- Supervise implemented commissioning, qualification, and validation strategies
- Lead Startup and CQV activities to ensure compliance with regulations and standards
- Oversee project plans for timely completion of CQV, post OQ, and startup deliverables
- Collaborate with cross-functional teams to identify and mitigate CAPEX investment risks
- Develop and maintain relationships with key stakeholders for successful project execution
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Boni & Prämien
- Compensation programs that recognize high performance
Sonstige Vorteile
- Lifestyle benefits
- Relocation assistance
Familienfreundlichkeit
- Family benefits
Mitarbeiterrabatte
- Leisure benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
- Inclusive workplace
Sinnstiftende Arbeit
- Ethical workplace
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens CH12 Lonza AG 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
CH12 Lonza AG
Branche
Pharmaceuticals
Beschreibung
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
Noch nicht perfekt?
- CH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Associate Director, Quality Strategy and Operations(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
Qualification CQV Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
Associate Director, QA SAP Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Head of CQV/CSV - Advanced Synthesis Conjugates(m/w/x)
Vollzeitnur vor OrtSeniorVisp