CH12 Lonza AG
QA Automation Specialist - Batch Record Review(m/w/x)
Full-timeOn-siteNot specified
Visp
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Quality assurance for electronic batch records and master production records within GMP pharmaceutical/API production. Solid experience in GMP pharmaceutical/API industry and eBR review required. Relocation assistance provided.
Requirements
- Academic degree in Chemistry, Biotechnology, Life Sciences, or related field
- Solid experience in GMP-regulated pharmaceutical/API industry
- Experience in electronic batch records (execution and/or review)
- Ability to recognize non-compliance and gaps in quality standards
- Structured, detailed, and well-organized work attitude; open-minded to new ideas; agile, highly motivated, and dynamic
- Business fluent English; good German language skills advantageous
Tasks
- Partner with internal customers on quality topics related to eBR setup
- Check and approve master production records for consistency
- Review completed batch records within specified timeframes
- Review minor deviations, investigations, and CAPAs by due dates
- Ensure closure and archiving of batch records after completion
- Assist in managing and tracking performance metrics and quality data
- Support QA department in various meetings
- Take on additional tasks as assigned
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Bonuses & Incentives
- Compensation programs that recognize high performance
Corporate Discounts
- Numerous lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Other Benefits
- Relocation assistance
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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Quality assurance for electronic batch records and master production records within GMP pharmaceutical/API production. Solid experience in GMP pharmaceutical/API industry and eBR review required. Relocation assistance provided.
Requirements
- Academic degree in Chemistry, Biotechnology, Life Sciences, or related field
- Solid experience in GMP-regulated pharmaceutical/API industry
- Experience in electronic batch records (execution and/or review)
- Ability to recognize non-compliance and gaps in quality standards
- Structured, detailed, and well-organized work attitude; open-minded to new ideas; agile, highly motivated, and dynamic
- Business fluent English; good German language skills advantageous
Tasks
- Partner with internal customers on quality topics related to eBR setup
- Check and approve master production records for consistency
- Review completed batch records within specified timeframes
- Review minor deviations, investigations, and CAPAs by due dates
- Ensure closure and archiving of batch records after completion
- Assist in managing and tracking performance metrics and quality data
- Support QA department in various meetings
- Take on additional tasks as assigned
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Bonuses & Incentives
- Compensation programs that recognize high performance
Corporate Discounts
- Numerous lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Other Benefits
- Relocation assistance
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.
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