CH12 Lonza AG
Manufacturing Specialist BioConjugates(m/w/x)
Full-timeOn-siteExperienced
Visp
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CHCH12 Lonza AG
Manufacturing Specialist Vibe-X(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Executing vaccine production activities in Upstream, Downstream, or Bioconjugates, troubleshooting equipment and processes. Bachelor/Master's in Biotech/Bio/Biochem Engineering or relevant experience, plus sound biotechnological process knowledge required. Relocation assistance available.
Requirements
- Completed chemical/biopharmaceutical education or corresponding training qualification
- Bachelor/Master's degree in Biotechnology, Biology, Biochemical Engineering or several years of relevant professional experience
- Sound knowledge of biotechnological processes in microbial and/or mammalian cultivation, protein purification, or Bioconjugates
- Excellent communication skills
- Teamwork skills
- Driven and solution-oriented attitude
- Fluency in English
- Fluency in German is considered a plus
- Basic GMP understanding is a plus
Tasks
- Support the project team in defining innovative vaccine production processes
- Collaborate on qualifying and validating new production areas and processes
- Execute manufacturing activities in Upstream Processing, Downstream Processing, or Bioconjugates according to cGMP and SOPs
- Evaluate test results and troubleshoot manufacturing equipment
- Make recommendations for resolving manufacturing issues
- Prepare risk assessments for Safety, Health, Environment, and Environmental Monitoring
- Assist in preparing documents like electronic batch records and SOPs for the production area
- Review production documentation and address deviations and change requests
- Implement CAPAs to maintain high-quality GMP standards
- Engage in capital investment projects for new manufacturing units as a manufacturing expert
- Deliver input for the setup, commissioning, and qualification of manufacturing suites and equipment
- Train manufacturing staff on specific equipment and standard operations
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Additional Allowances
- Relocation assistance for eligible candidates
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CH12 Lonza AG 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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CHCH12 Lonza AG
Manufacturing Specialist Vibe-X(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Executing vaccine production activities in Upstream, Downstream, or Bioconjugates, troubleshooting equipment and processes. Bachelor/Master's in Biotech/Bio/Biochem Engineering or relevant experience, plus sound biotechnological process knowledge required. Relocation assistance available.
Requirements
- Completed chemical/biopharmaceutical education or corresponding training qualification
- Bachelor/Master's degree in Biotechnology, Biology, Biochemical Engineering or several years of relevant professional experience
- Sound knowledge of biotechnological processes in microbial and/or mammalian cultivation, protein purification, or Bioconjugates
- Excellent communication skills
- Teamwork skills
- Driven and solution-oriented attitude
- Fluency in English
- Fluency in German is considered a plus
- Basic GMP understanding is a plus
Tasks
- Support the project team in defining innovative vaccine production processes
- Collaborate on qualifying and validating new production areas and processes
- Execute manufacturing activities in Upstream Processing, Downstream Processing, or Bioconjugates according to cGMP and SOPs
- Evaluate test results and troubleshoot manufacturing equipment
- Make recommendations for resolving manufacturing issues
- Prepare risk assessments for Safety, Health, Environment, and Environmental Monitoring
- Assist in preparing documents like electronic batch records and SOPs for the production area
- Review production documentation and address deviations and change requests
- Implement CAPAs to maintain high-quality GMP standards
- Engage in capital investment projects for new manufacturing units as a manufacturing expert
- Deliver input for the setup, commissioning, and qualification of manufacturing suites and equipment
- Train manufacturing staff on specific equipment and standard operations
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Additional Allowances
- Relocation assistance for eligible candidates
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CH12 Lonza AG 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
CH12 Lonza AG
Industry
Pharmaceuticals
Description
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
Not a perfect match?
- CH12 Lonza AG
Manufacturing Specialist BioConjugates(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Manufacturing Specialist Mammalian(m/w/x)
Full-timeOn-siteNot specifiedVisp - Lonza
Manufacturing Specialist, BMS(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Manufacturing Specialist PCP(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Manufacturing Specialist Mammalian 100%(m/w/x)
Full-timeOn-siteExperiencedVisp