CH12 Lonza AG
Manufacturing Specialist Mammalian 100%(m/w/x)
Full-timeOn-siteExperienced
Visp
New Job?Nejo!
The AI Job Search Engine
CHCH12 Lonza AG
Manufacturing Specialist Mammalian(m/w/x)
Visp
Full-timeOn-site
Nejo AI Summary
Manufacturing biopharmaceutical products from eukaryotic cell cultures in cGMP Upstream/Downstream Processing, including equipment troubleshooting. Bachelor/Master's in Biotech/Bioengineering or similar, with eukaryotic cell cultivation process knowledge essential. 4-shift system work.
Requirements
- Completed chemical/biopharmaceutical education or corresponding training qualification, Bachelor/Master's degree in Biotechnology, Biology, Biochemical Engineering or related disciplines
- Sound knowledge of biotechnological processes in microbial and/or mammalian cultivation or protein purification
- Excellent communication skills, teamwork, driven, and solution-oriented
- Fluency in English, fluency in German is a plus
- Openness to work in shift (4-shift system)
- Basic GMP understanding is a plus
Tasks
- Execute manufacturing activities in Upstream or Downstream Processing according to cGMP guidelines
- Evaluate test results and troubleshoot manufacturing equipment
- Resolve issues and make recommendations for resolution
- Support preparation of SHE, EM, and risk assessments for assigned products
- Assist in preparing documents like electronic batch records and SOPs
- 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
- Deliver input for the setup, commissioning, and qualification of manufacturing suites and equipment
- Train manufacturing staff on specific equipment and standard operations
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
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.
Not a perfect match?
- Lonza
Manufacturing Specialist, BMS(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Manufacturing Specialist(m/w/x)
Full-timeOn-siteJuniorVisp - CH12 Lonza AG
Manufacturing Specialist BioConjugates(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Manufacturing Specialist Vibe-X(m/w/x)
Full-timeOn-siteExperiencedVisp
CHCH12 Lonza AG
Manufacturing Specialist Mammalian(m/w/x)
Visp
Full-timeOn-site
Nejo AI Summary
Manufacturing biopharmaceutical products from eukaryotic cell cultures in cGMP Upstream/Downstream Processing, including equipment troubleshooting. Bachelor/Master's in Biotech/Bioengineering or similar, with eukaryotic cell cultivation process knowledge essential. 4-shift system work.
Requirements
- Completed chemical/biopharmaceutical education or corresponding training qualification, Bachelor/Master's degree in Biotechnology, Biology, Biochemical Engineering or related disciplines
- Sound knowledge of biotechnological processes in microbial and/or mammalian cultivation or protein purification
- Excellent communication skills, teamwork, driven, and solution-oriented
- Fluency in English, fluency in German is a plus
- Openness to work in shift (4-shift system)
- Basic GMP understanding is a plus
Tasks
- Execute manufacturing activities in Upstream or Downstream Processing according to cGMP guidelines
- Evaluate test results and troubleshoot manufacturing equipment
- Resolve issues and make recommendations for resolution
- Support preparation of SHE, EM, and risk assessments for assigned products
- Assist in preparing documents like electronic batch records and SOPs
- 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
- Deliver input for the setup, commissioning, and qualification of manufacturing suites and equipment
- Train manufacturing staff on specific equipment and standard operations
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
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 Mammalian 100%(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Manufacturing Specialist, BMS(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Manufacturing Specialist(m/w/x)
Full-timeOn-siteJuniorVisp - CH12 Lonza AG
Manufacturing Specialist BioConjugates(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Manufacturing Specialist Vibe-X(m/w/x)
Full-timeOn-siteExperiencedVisp