The AI Job Search Engine
Associate Director Operation Readiness Lead(m/w/x)
Description
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.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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
Education
Work Experience
approx. 1 - 4 years
Tasks
- •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
Languages
German – Business Fluent
English – Business Fluent
Benefits
Bonuses & Incentives
- •Compensation programs that recognize high performance
Other Benefits
- •Lifestyle benefits
- •Relocation assistance
Family Support
- •Family benefits
Corporate Discounts
- •Leisure benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
- •Inclusive workplace
Purpose-Driven Work
- •Ethical workplace
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
- Lonza
Qualification CQV Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Director Manufacturing Lead(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
(Senior-) Program Manager, Advanced Synthesis(m/w/x)
Full-timeOn-siteManagementVisp - CH12 Lonza AG
CQV Engineer / Qualification & Validation Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp
Associate Director Operation Readiness Lead(m/w/x)
The AI Job Search Engine
Description
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.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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
Education
Work Experience
approx. 1 - 4 years
Tasks
- •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
Languages
German – Business Fluent
English – Business Fluent
Benefits
Bonuses & Incentives
- •Compensation programs that recognize high performance
Other Benefits
- •Lifestyle benefits
- •Relocation assistance
Family Support
- •Family benefits
Corporate Discounts
- •Leisure benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
- •Inclusive workplace
Purpose-Driven Work
- •Ethical workplace
About the Company
CH12 Lonza AG
Industry
Pharmaceuticals
Description
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)
Full-timeOn-siteSeniorVisp - Lonza
Qualification CQV Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Director Manufacturing Lead(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
(Senior-) Program Manager, Advanced Synthesis(m/w/x)
Full-timeOn-siteManagementVisp - CH12 Lonza AG
CQV Engineer / Qualification & Validation Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp