Lonza
Process Expert MSAT(m/w/x)
Full-timeOn-siteSenior
Visp
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LOLonza
Manufacturing Process Expert Lead(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Optimizing daily GMP operations and improving process robustness for medicines manufacturing. Bachelor's degree or equivalent experience required. International assignment opportunity, collaborative environment.
Requirements
- Bachelor’s degree in scientific or engineering field, or equivalent relevant experience and learning
- Experience in GMP manufacturing, pharmaceutical operations, biotechnology, or similar regulated environment
- Ability to contribute to equipment and process introduction activities, familiarity with FAT/SAT and qualification steps beneficial
- Clear and supportive communication skills, ability to train and collaborate with colleagues
- Practical approach to problem-solving, using structured methods for root cause analysis and improvements
- Proactive, organized mindset, ability to balance multiple activities while maintaining commitment to safety, quality, and continuous improvement
Tasks
- Optimize daily GMP operations
- Improve process robustness
- Ensure safe, compliant, and timely production
- Support capability expansion
- Lead daily manufacturing activities in GMP environment
- Partner with cross-functional teams for new equipment
- Contribute to user requirements and project milestones
- Prepare manufacturing areas for operations
- Update documentation and ensure equipment readiness
- Perform standard checks before batch activities
- Train colleagues on new processes and safety practices
- Foster a culture of learning and team development
- Troubleshoot and solve problems with experts
- Implement effective operational improvements
- Use continuous-improvement tools to enhance efficiency
- Represent manufacturing during audits and transfers
- Support early production campaigns with new technologies
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Workation & Sabbatical
- International assignment opportunity
Informal Culture
- Collaborative environment
- Teamwork and inclusion
Learning & Development
- Professional development programs
Purpose-Driven Work
- Ethical workplace
Other Benefits
- Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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LOLonza
Manufacturing Process Expert Lead(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Optimizing daily GMP operations and improving process robustness for medicines manufacturing. Bachelor's degree or equivalent experience required. International assignment opportunity, collaborative environment.
Requirements
- Bachelor’s degree in scientific or engineering field, or equivalent relevant experience and learning
- Experience in GMP manufacturing, pharmaceutical operations, biotechnology, or similar regulated environment
- Ability to contribute to equipment and process introduction activities, familiarity with FAT/SAT and qualification steps beneficial
- Clear and supportive communication skills, ability to train and collaborate with colleagues
- Practical approach to problem-solving, using structured methods for root cause analysis and improvements
- Proactive, organized mindset, ability to balance multiple activities while maintaining commitment to safety, quality, and continuous improvement
Tasks
- Optimize daily GMP operations
- Improve process robustness
- Ensure safe, compliant, and timely production
- Support capability expansion
- Lead daily manufacturing activities in GMP environment
- Partner with cross-functional teams for new equipment
- Contribute to user requirements and project milestones
- Prepare manufacturing areas for operations
- Update documentation and ensure equipment readiness
- Perform standard checks before batch activities
- Train colleagues on new processes and safety practices
- Foster a culture of learning and team development
- Troubleshoot and solve problems with experts
- Implement effective operational improvements
- Use continuous-improvement tools to enhance efficiency
- Represent manufacturing during audits and transfers
- Support early production campaigns with new technologies
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Workation & Sabbatical
- International assignment opportunity
Informal Culture
- Collaborative environment
- Teamwork and inclusion
Learning & Development
- Professional development programs
Purpose-Driven Work
- Ethical workplace
Other Benefits
- Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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?
- Lonza
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