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Designing and implementing upstream bioprocesses at manufacturing scale for microbial products at a global pharma manufacturer. 5+ years in biopharma manufacturing with fermentation processes and GMP understanding required. High performance compensation programs, relocation assistance.
Requirements
- Master's degree, PhD, or equivalent experience (plus)
- Preferred study in Biotechnology, chemical engineering, or related areas
- More than 5 years in biopharma manufacturing and/or process development (preferable in Microbial Manufacturing)
- Solid understanding and experience with fermentation processes and primary recovery unit operations
- GMP and deep understanding of bioprocess technology
- Fluency in English and German
- Strong leadership skills
- Very good communication skills and interaction with interfaces
- Strong team orientation
- Structured, focused, and well-organized working attitude
- Open-mindedness for new ideas and suggestions
- Agile, highly motivated, and dynamic drive
- Problem-solving skills
Tasks
- Lead cross-functional teams
- Manage technology transfers
- Design and upscale processes
- Implement processes at manufacturing scale
- Oversee project lifecycles
- Liaise between process donors and operations
- Ensure process scalability and manufacturability
- Ensure successful technology transfer using formal processes
- Manage information transfer during technology transfer
- Manage process risks and change control
- Resolve manufacturing process issues
- Perform GMP risk analysis for manufacturing processes
- Implement manufacturing processes in the plant
- Interact with customers during tech transfer and campaigns
- Report daily batch status and performance
- Promptly compile process deviations, change requests, and campaign reports
- Compile CMC sections for filing documents
- Compile technical content for validation reports
- Contribute to developing and implementing MSAT procedures
- Drive continuous process improvement
- Supervise local and global MSAT initiatives
- Lead major task forces or troubleshooting teams
- Evaluate and drive innovative trends
- Mentor scientific and production staff
- Perform process-specific training for staff
Work Experience
- 5 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Bonuses & Incentives
- High performance compensation programs
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
- Inclusive workplace
Purpose-Driven Work
- Ethical workplace
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- LonzaFull-timeOn-siteManagementVisp
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Head Manufacturing Science and Technology(m/w/x)
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Designing and implementing upstream bioprocesses at manufacturing scale for microbial products at a global pharma manufacturer. 5+ years in biopharma manufacturing with fermentation processes and GMP understanding required. High performance compensation programs, relocation assistance.
Requirements
- Master's degree, PhD, or equivalent experience (plus)
- Preferred study in Biotechnology, chemical engineering, or related areas
- More than 5 years in biopharma manufacturing and/or process development (preferable in Microbial Manufacturing)
- Solid understanding and experience with fermentation processes and primary recovery unit operations
- GMP and deep understanding of bioprocess technology
- Fluency in English and German
- Strong leadership skills
- Very good communication skills and interaction with interfaces
- Strong team orientation
- Structured, focused, and well-organized working attitude
- Open-mindedness for new ideas and suggestions
- Agile, highly motivated, and dynamic drive
- Problem-solving skills
Tasks
- Lead cross-functional teams
- Manage technology transfers
- Design and upscale processes
- Implement processes at manufacturing scale
- Oversee project lifecycles
- Liaise between process donors and operations
- Ensure process scalability and manufacturability
- Ensure successful technology transfer using formal processes
- Manage information transfer during technology transfer
- Manage process risks and change control
- Resolve manufacturing process issues
- Perform GMP risk analysis for manufacturing processes
- Implement manufacturing processes in the plant
- Interact with customers during tech transfer and campaigns
- Report daily batch status and performance
- Promptly compile process deviations, change requests, and campaign reports
- Compile CMC sections for filing documents
- Compile technical content for validation reports
- Contribute to developing and implementing MSAT procedures
- Drive continuous process improvement
- Supervise local and global MSAT initiatives
- Lead major task forces or troubleshooting teams
- Evaluate and drive innovative trends
- Mentor scientific and production staff
- Perform process-specific training for staff
Work Experience
- 5 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Bonuses & Incentives
- High performance compensation programs
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
- Inclusive workplace
Purpose-Driven Work
- Ethical workplace
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?
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