Lonza
QA Specialist, Batch Record Review(m/w/x)
Full-timeOn-siteJunior
Visp
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Reviewing executed electronic batch records in MES Syncade for biopharmaceutical manufacturing. Experience in batch record review and professional English/basic German proficiency required. Relocation assistance, performance-based compensation programs.
Requirements
- Degree in Pharmacy, Engineering, or equivalent
- Understanding of GMP and bioprocess manufacturing
- Ability to identify Quality standard gaps
- Experience in batch record review or manufacturing
- Professional English and basic German proficiency
- Structured, precise, and well-organized working attitude
- Open-mindedness and pragmatism for new ideas
Tasks
- Review executed electronic batch records in MES Syncade
- Ensure batch records are accurate and complete
- Verify process steps follow intended designs
- Confirm documentation adheres to GDP requirements
- Identify and address record deviations or discrepancies
- Manage Quality Records including CAPAs and investigations
- Resolve batch record execution issues for operations
- Participate in MES Syncade recipe improvements
- Facilitate batch release through timely record closure
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GMP
- eBR
Benefits
Career Advancement
- Agile career
Startup Environment
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Bonuses & Incentives
- Performance-based compensation programs
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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Reviewing executed electronic batch records in MES Syncade for biopharmaceutical manufacturing. Experience in batch record review and professional English/basic German proficiency required. Relocation assistance, performance-based compensation programs.
Requirements
- Degree in Pharmacy, Engineering, or equivalent
- Understanding of GMP and bioprocess manufacturing
- Ability to identify Quality standard gaps
- Experience in batch record review or manufacturing
- Professional English and basic German proficiency
- Structured, precise, and well-organized working attitude
- Open-mindedness and pragmatism for new ideas
Tasks
- Review executed electronic batch records in MES Syncade
- Ensure batch records are accurate and complete
- Verify process steps follow intended designs
- Confirm documentation adheres to GDP requirements
- Identify and address record deviations or discrepancies
- Manage Quality Records including CAPAs and investigations
- Resolve batch record execution issues for operations
- Participate in MES Syncade recipe improvements
- Facilitate batch release through timely record closure
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GMP
- eBR
Benefits
Career Advancement
- Agile career
Startup Environment
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Bonuses & Incentives
- Performance-based compensation programs
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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