Lonza
QA Specialist, Batch Record Review(m/w/x)
Full-timeOn-siteJunior
Visp
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LOLonza
Intern - QA Specialist Batch Record Review(m/w/x)
Visp
Full-timeInternshipOn-site
Nejo AI Summary
Reviewing electronic GMP batch records for pharmaceutical manufacturing. Previous GMP experience and ability to identify compliance gaps required. Agile career path, dynamic work culture.
Requirements
- Bachelor degree or relevant work/internship experience in Biology, Chemistry, Biotechnology, Life Science or related field
- Previous GMP regulated pharmaceutical/API industry experience
- Ability to identify non-compliance and gaps from quality standards
- Structured, precise, well-organized working attitude
- Open-minded for new ideas and suggestions
- Agile, highly motivated, dynamic drive
- Fluent English
- Good to have German
Tasks
- Support Quality Assurance team in reviewing electronic GMP documentation
- Verify and organize manufacturing batch records
- Gain hands-on experience in regulated industry practices
- Ensure data integrity and compliance with internal procedures
- Work with QA specialists and cross-functional teams
- Review executed batch records including cleaning logs, production documentation, temperature reports, test procedures, raw data, and logbooks
- Add review comments to executed batch records
- Clarify issues with the operations team
- Evaluate observations with the responsible QA Manager
- Initiate deviations and investigations for batch record review findings
Education
- Bachelor's degree
Languages
- English – Fluent
- German – Basic
Benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Bonuses & Incentives
- Compensation programs for high performance
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
Intern - QA Specialist Batch Record Review(m/w/x)
Visp
Full-timeInternshipOn-site
Nejo AI Summary
Reviewing electronic GMP batch records for pharmaceutical manufacturing. Previous GMP experience and ability to identify compliance gaps required. Agile career path, dynamic work culture.
Requirements
- Bachelor degree or relevant work/internship experience in Biology, Chemistry, Biotechnology, Life Science or related field
- Previous GMP regulated pharmaceutical/API industry experience
- Ability to identify non-compliance and gaps from quality standards
- Structured, precise, well-organized working attitude
- Open-minded for new ideas and suggestions
- Agile, highly motivated, dynamic drive
- Fluent English
- Good to have German
Tasks
- Support Quality Assurance team in reviewing electronic GMP documentation
- Verify and organize manufacturing batch records
- Gain hands-on experience in regulated industry practices
- Ensure data integrity and compliance with internal procedures
- Work with QA specialists and cross-functional teams
- Review executed batch records including cleaning logs, production documentation, temperature reports, test procedures, raw data, and logbooks
- Add review comments to executed batch records
- Clarify issues with the operations team
- Evaluate observations with the responsible QA Manager
- Initiate deviations and investigations for batch record review findings
Education
- Bachelor's degree
Languages
- English – Fluent
- German – Basic
Benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Bonuses & Incentives
- Compensation programs for high performance
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?
- Lonza
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(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
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