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Associate Director Operation Readiness Lead(m/w/x)
Beschreibung
As an Operations Readiness Lead, you will ensure that projects are set for success by managing resources, timelines, and compliance. This role involves collaborating with teams to mitigate risks and maintain strong stakeholder relationships, making each day dynamic and impactful.
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Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
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
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
- CH12 Lonza AGVollzeitnur vor OrtSeniorVisp
- Lonza
Qualification CQV Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Director Manufacturing Lead(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
(Senior-) Program Manager, Advanced Synthesis(m/w/x)
Vollzeitnur vor OrtManagementVisp - CH12 Lonza AG
CQV Engineer / Qualification & Validation Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp
Associate Director Operation Readiness Lead(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
As an Operations Readiness Lead, you will ensure that projects are set for success by managing resources, timelines, and compliance. This role involves collaborating with teams to mitigate risks and maintain strong stakeholder relationships, making each day dynamic and impactful.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
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
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
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.
- CH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Qualification CQV Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Director Manufacturing Lead(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
(Senior-) Program Manager, Advanced Synthesis(m/w/x)
Vollzeitnur vor OrtManagementVisp - CH12 Lonza AG
CQV Engineer / Qualification & Validation Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp