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Leading MES projects from analysis to deployment in pharmaceutical manufacturing. GMP and validated systems experience required. Relocation assistance, lifestyle and family benefits.
Requirements
- University degree in Computer Science, Industrial IT/OT, Automation Engineering, or related field (Bachelor level or higher)
- Professional experience in IT/OT, MES, or automation engineering in regulated environment
- Understanding of GMP requirements and experience with validated systems
- Responsibility for MES lifecycle (operation, enhancements, release, interface coordination)
- Knowledge of OT networks, virtualization (VMware), system architectures, cybersecurity principles
- Fluent German or English (minimum B2 level)
- Structured, independent working style, communication and problem-solving skills
- Willingness to participate in on-call duty (2-3 times per year)
Tasks
- Lead MES projects through all lifecycle phases
- Conduct requirement analysis, design, implementation, testing, and deployment
- Maintain and optimize MES standards
- Ensure compliance with site and global guidelines
- Enhance and update MES systems for reliable operation
- Collaborate with Operations, QA, Automation, and IT/OT teams
- Analyze and improve MES workflows
- Identify opportunities for digitalization and efficiency
- Manage external partners and vendors
- Ensure GMP-compliant execution of MES and OT activities
- Maintain GMP-compliant documentation
- Manage change control and validation readiness
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- MES
- VMware
Benefits
Bonuses & Incentives
- Compensation programs recognizing high performance
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Startup Environment
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
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Leading MES projects from analysis to deployment in pharmaceutical manufacturing. GMP and validated systems experience required. Relocation assistance, lifestyle and family benefits.
Requirements
- University degree in Computer Science, Industrial IT/OT, Automation Engineering, or related field (Bachelor level or higher)
- Professional experience in IT/OT, MES, or automation engineering in regulated environment
- Understanding of GMP requirements and experience with validated systems
- Responsibility for MES lifecycle (operation, enhancements, release, interface coordination)
- Knowledge of OT networks, virtualization (VMware), system architectures, cybersecurity principles
- Fluent German or English (minimum B2 level)
- Structured, independent working style, communication and problem-solving skills
- Willingness to participate in on-call duty (2-3 times per year)
Tasks
- Lead MES projects through all lifecycle phases
- Conduct requirement analysis, design, implementation, testing, and deployment
- Maintain and optimize MES standards
- Ensure compliance with site and global guidelines
- Enhance and update MES systems for reliable operation
- Collaborate with Operations, QA, Automation, and IT/OT teams
- Analyze and improve MES workflows
- Identify opportunities for digitalization and efficiency
- Manage external partners and vendors
- Ensure GMP-compliant execution of MES and OT activities
- Maintain GMP-compliant documentation
- Manage change control and validation readiness
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- MES
- VMware
Benefits
Bonuses & Incentives
- Compensation programs recognizing high performance
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Startup Environment
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Lonza
Industry
Pharmaceuticals
Description
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Not a perfect match?
- CH12 Lonza AG
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MES Expert Drug Product(m/w/x)
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Teamleiter EI&C MES(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Digital Innovation Specialist(m/w/x)
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DeltaV Electrical Instrumentation & Control Engineer(m/w/x)
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