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Defining process technology strategy and driving facility design for bioconjugates and advanced synthesis manufacturing. 8+ years MSAT or process engineering experience in GMP pharma/biotech required. International assignment opportunity, professional development programs.
Requirements
- 8+ years MSAT, process engineering, or technical operations in GMP pharma/biotech
- Bachelor's degree in chemical/Bioprocess Engineering or related field
- Strong expertise in process equipment, PAT, and manufacturing technologies
- Experience in bioconjugates and/or advanced synthesis
- Translate product requirements into scalable manufacturing solutions
- Support facility startup, commissioning, and tech transfer
- Strong analytical and problem-solving skills
- Familiarity with automation systems, process control, data integrity
- Excellent communication and stakeholder management skills
- Collaborative mindset and cross-functional influence
- Willingness to travel to EMEA and NA approx. 20%
Tasks
- Define process technology strategy
- Drive facility design and technology selection
- Ensure scalable and GMP-compliant processes
- Support process technology strategy
- Lead process equipment selection
- Implement process analytical technology (PAT)
- Collaborate with internal teams and customers
- Understand product requirements
- Identify critical quality attributes (CQAs)
- Consider process parameters and scale-up
- Develop production models
- Support facility design
- Plan operational activities
- Evaluate technology solutions
- Recommend balanced technology options
- Provide technical input
- Contribute to user requirement specifications (URS)
- Create process flow diagrams
- Design equipment layouts
- Partner with automation and OT teams
- Integrate process control and PAT strategies
- Support commissioning activities
- Conduct FAT and SAT
- Interface with stakeholders
- Manage design, construction, and startup
Work Experience
- 8 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- MSAT
- PAT
- automation systems
- process control strategies
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
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- LonzaFull-timeOn-siteExperiencedVisp
- CH12 Lonza AG
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Defining process technology strategy and driving facility design for bioconjugates and advanced synthesis manufacturing. 8+ years MSAT or process engineering experience in GMP pharma/biotech required. International assignment opportunity, professional development programs.
Requirements
- 8+ years MSAT, process engineering, or technical operations in GMP pharma/biotech
- Bachelor's degree in chemical/Bioprocess Engineering or related field
- Strong expertise in process equipment, PAT, and manufacturing technologies
- Experience in bioconjugates and/or advanced synthesis
- Translate product requirements into scalable manufacturing solutions
- Support facility startup, commissioning, and tech transfer
- Strong analytical and problem-solving skills
- Familiarity with automation systems, process control, data integrity
- Excellent communication and stakeholder management skills
- Collaborative mindset and cross-functional influence
- Willingness to travel to EMEA and NA approx. 20%
Tasks
- Define process technology strategy
- Drive facility design and technology selection
- Ensure scalable and GMP-compliant processes
- Support process technology strategy
- Lead process equipment selection
- Implement process analytical technology (PAT)
- Collaborate with internal teams and customers
- Understand product requirements
- Identify critical quality attributes (CQAs)
- Consider process parameters and scale-up
- Develop production models
- Support facility design
- Plan operational activities
- Evaluate technology solutions
- Recommend balanced technology options
- Provide technical input
- Contribute to user requirement specifications (URS)
- Create process flow diagrams
- Design equipment layouts
- Partner with automation and OT teams
- Integrate process control and PAT strategies
- Support commissioning activities
- Conduct FAT and SAT
- Interface with stakeholders
- Manage design, construction, and startup
Work Experience
- 8 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- MSAT
- PAT
- automation systems
- process control strategies
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
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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MSAT Expert Drug Product(m/w/x)
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USP Process Expert MSAT Microbial(m/w/x)
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