Lonza
MSAT Process Expert Mammalian Upstream Large-Scale(m/w/x)
Full-timeOn-siteSenior
Visp
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Transfer, scale-up, and optimization of mammalian/purification manufacturing at a global biopharmaceutical CMO. Five years biopharmaceutical manufacturing or process development experience required; mammalian cell or purification expertise preferred. Contribution to MSAT toolbox development.
Requirements
- PhD (preferred), Master’s or Bachelor degree in biotechnology, chemical engineering or related disciplines
- Minimum five years industry experience in biopharmaceutical manufacturing or process development
- Strong preference for expertise in mammalian cell based and/or purification focused operation
- Understanding of GMP and bioprocess technology
- Very good communication and interaction skills
- Fluency in English
Tasks
- Transfer mammalian/purification manufacturing processes.
- Scale up mammalian/purification manufacturing processes.
- Supervise mammalian/purification manufacturing processes.
- Optimize mammalian/purification manufacturing processes.
- Contribute to developing the MSAT toolbox.
- Act as a long-term process owner.
- Lead cross-functional teams for technology transfers.
- Lead teams for process design and scaling-up.
- Implement processes at manufacturing scale.
- Manage the full product lifecycle of assigned projects.
- Act as interface between process donors and operations.
- Ensure process scalability.
- Ensure process manufacturability.
- Ensure successful technology transfer.
- Manage information transfer, process risks, and change control.
- Resolve manufacturing process issues.
- Ensure regulatory compliance during issue resolution.
- Perform 24/7 on-call duty.
- Perform GMP risk analysis for manufacturing processes.
- Interact with customers during tech transfer and campaigns.
- Provide daily reports on batch status and performance.
- Prepare timely process deviations, change requests, campaign reports.
- Drive continuous improvement of process performance.
Work Experience
- 5 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
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.
Not a perfect match?
- Lonza
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Full-timeOn-siteManagementVisp - Lonza
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MSAT Bioconjugates Process Expert(m/w/x)
Full-timeOn-siteExperiencedVisp
Transfer, scale-up, and optimization of mammalian/purification manufacturing at a global biopharmaceutical CMO. Five years biopharmaceutical manufacturing or process development experience required; mammalian cell or purification expertise preferred. Contribution to MSAT toolbox development.
Requirements
- PhD (preferred), Master’s or Bachelor degree in biotechnology, chemical engineering or related disciplines
- Minimum five years industry experience in biopharmaceutical manufacturing or process development
- Strong preference for expertise in mammalian cell based and/or purification focused operation
- Understanding of GMP and bioprocess technology
- Very good communication and interaction skills
- Fluency in English
Tasks
- Transfer mammalian/purification manufacturing processes.
- Scale up mammalian/purification manufacturing processes.
- Supervise mammalian/purification manufacturing processes.
- Optimize mammalian/purification manufacturing processes.
- Contribute to developing the MSAT toolbox.
- Act as a long-term process owner.
- Lead cross-functional teams for technology transfers.
- Lead teams for process design and scaling-up.
- Implement processes at manufacturing scale.
- Manage the full product lifecycle of assigned projects.
- Act as interface between process donors and operations.
- Ensure process scalability.
- Ensure process manufacturability.
- Ensure successful technology transfer.
- Manage information transfer, process risks, and change control.
- Resolve manufacturing process issues.
- Ensure regulatory compliance during issue resolution.
- Perform 24/7 on-call duty.
- Perform GMP risk analysis for manufacturing processes.
- Interact with customers during tech transfer and campaigns.
- Provide daily reports on batch status and performance.
- Prepare timely process deviations, change requests, campaign reports.
- Drive continuous improvement of process performance.
Work Experience
- 5 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
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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