CH12 Lonza AG
MSAT Drug Product - Internship(m/w/x)
Full-timeInternshipOn-site
Visp
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LOLonza
Internship MSAT Material Management / MSAT Process Expert(m/w/x)
Visp
Full-timeInternshipOn-site
Nejo AI Summary
Support material management in microbial cGMP manufacturing, mitigating quality issues and qualifying single-use assemblies. Bachelor's or Master's degree in a scientific/technical discipline required. Career growth opportunities, inclusive culture.
Requirements
- Bachelor's or Master's degree in Biotechnology, Chemistry, Chemical, Biochemical Engineering, Pharmacy, or related scientific/technical discipline
- Strong interest in microbial manufacturing processes and process lifecycle management
- Basic understanding of bioprocess fundamentals (microbial upstream/downstream, process parameters, impact on product quality)
- High attention to detail and interest in technical documentation and data integrity
- Strong interest in GMP environments and regulated manufacturing
- Good organizational and planning skills, ability to manage multiple tasks/timelines
- Ability to work effectively in cross-functional teams (Manufacturing, Quality, Quality Control)
- Structured, analytical mindset with problem-solving orientation
- Good English knowledge, written and spoken
Tasks
- Support material management in microbial cGMP manufacturing
- Mitigate material quality issues
- Design and qualify single-use assemblies
- Coordinate stakeholder inputs for document preparation
- Monitor activity progress and identify delays
- Escalate issues and risks to MSAT process expert lead
- Review and analyze material management data
- Support MSAT process expert activities throughout project lifecycle
- Resolve process issues during manufacturing
- Conduct GMP risk analysis for manufacturing processes
- Compile process-related deviations and change requests
- Support continuous improvement projects
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Advanced
Benefits
Career Advancement
- Career growth opportunities
Informal Culture
- Inclusive, ethical, supportive culture
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
Internship MSAT Material Management / MSAT Process Expert(m/w/x)
Visp
Full-timeInternshipOn-site
Nejo AI Summary
Support material management in microbial cGMP manufacturing, mitigating quality issues and qualifying single-use assemblies. Bachelor's or Master's degree in a scientific/technical discipline required. Career growth opportunities, inclusive culture.
Requirements
- Bachelor's or Master's degree in Biotechnology, Chemistry, Chemical, Biochemical Engineering, Pharmacy, or related scientific/technical discipline
- Strong interest in microbial manufacturing processes and process lifecycle management
- Basic understanding of bioprocess fundamentals (microbial upstream/downstream, process parameters, impact on product quality)
- High attention to detail and interest in technical documentation and data integrity
- Strong interest in GMP environments and regulated manufacturing
- Good organizational and planning skills, ability to manage multiple tasks/timelines
- Ability to work effectively in cross-functional teams (Manufacturing, Quality, Quality Control)
- Structured, analytical mindset with problem-solving orientation
- Good English knowledge, written and spoken
Tasks
- Support material management in microbial cGMP manufacturing
- Mitigate material quality issues
- Design and qualify single-use assemblies
- Coordinate stakeholder inputs for document preparation
- Monitor activity progress and identify delays
- Escalate issues and risks to MSAT process expert lead
- Review and analyze material management data
- Support MSAT process expert activities throughout project lifecycle
- Resolve process issues during manufacturing
- Conduct GMP risk analysis for manufacturing processes
- Compile process-related deviations and change requests
- Support continuous improvement projects
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Advanced
Benefits
Career Advancement
- Career growth opportunities
Informal Culture
- Inclusive, ethical, supportive culture
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.
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?
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