Lonza
QA Specialist, Batch Record Review(m/w/x)
Full-timeOn-siteJunior
Visp
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CHCH12 Lonza AG
QA Automation Specialist - Batch Record Review(m/w/x)
Visp
Full-timeOn-site
Nejo AI Summary
Reviewing executed electronic batch records in MES Syncade for bioprocess manufacturing. University degree in Life Science or similar, with GMP knowledge and professional English fluency, required. Relocation assistance provided.
Requirements
- Basic GMP knowledge
- University degree in Biology, Biotechnology, Life Science, or similar educational background
- Basic understanding of GMP and bioprocess manufacturing
- Ability to identify non-compliance and gaps from Quality standards
- Professional fluency in English and basic German proficiency or willingness to learn
- Structured, precise, and well-organized working attitude; open-minded and pragmatic for new ideas and suggestions
Tasks
- Review executed electronic batch records in MES Syncade
- Participate in MES Syncade Recipe change management
- Collaborate with the Operations team to clarify ambiguities in batch records
- Manage Quality Records for Batch Record review observations
- Ensure completeness of documentation for batch release
- Engage with customers on batch record review and automation topics
- Collect and evaluate KPI data regularly
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Other Benefits
- Lifestyle benefits
- Relocation assistance
Family Support
- Family benefits
Corporate Discounts
- Leisure benefits
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
QA Automation Specialist - Batch Record Review(m/w/x)
Visp
Full-timeOn-site
Nejo AI Summary
Reviewing executed electronic batch records in MES Syncade for bioprocess manufacturing. University degree in Life Science or similar, with GMP knowledge and professional English fluency, required. Relocation assistance provided.
Requirements
- Basic GMP knowledge
- University degree in Biology, Biotechnology, Life Science, or similar educational background
- Basic understanding of GMP and bioprocess manufacturing
- Ability to identify non-compliance and gaps from Quality standards
- Professional fluency in English and basic German proficiency or willingness to learn
- Structured, precise, and well-organized working attitude; open-minded and pragmatic for new ideas and suggestions
Tasks
- Review executed electronic batch records in MES Syncade
- Participate in MES Syncade Recipe change management
- Collaborate with the Operations team to clarify ambiguities in batch records
- Manage Quality Records for Batch Record review observations
- Ensure completeness of documentation for batch release
- Engage with customers on batch record review and automation topics
- Collect and evaluate KPI data regularly
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Other Benefits
- Lifestyle benefits
- Relocation assistance
Family Support
- Family benefits
Corporate Discounts
- Leisure benefits
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.
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