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Associate Director Operation Readiness Lead(m/w/x)
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.
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
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
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
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
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- CH12 Lonza AGFull-timeOn-siteSeniorVisp
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Associate Director Operation Readiness Lead(m/w/x)
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.
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
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
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
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.
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