CH12 Lonza AG
QA Automation Specialist - Batch Record Review(m/w/x)
Full-timeOn-siteNot specified
Visp
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Reviewing executed batch records and production documentation for pharmaceutical batch releases. Degree in Biology, Chemistry, Biotechnology, or related field, with GMP pharmaceutical experience preferred. Relocation assistance.
Requirements
- Degree in Biology, Chemistry, Biotechnology, or related field
- Advantageous experience in GMP pharmaceutical or API industry
- Ability to identify non-compliance and quality gaps
- Structured, precise, and well-organized working attitude
- Openness to new ideas and suggestions
- Agile, highly motivated, and dynamic drive
- Business fluent English
- Preferred good command of German
Tasks
- Review executed batch records and production documentation
- Examine test procedures, raw data, and logbooks
- Ensure documentation completeness to support batch releases
- Evaluate batch record comments with operations and QA managers
- Support deviations and investigations for review observations
- Collect and evaluate regular KPI data
- Write and revise SOPs within your area of expertise
- Collaborate with quality and operations functions
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- GMP
- API
Benefits
Bonuses & Incentives
- High performance compensation programs
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
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.
Not a perfect match?
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Reviewing executed batch records and production documentation for pharmaceutical batch releases. Degree in Biology, Chemistry, Biotechnology, or related field, with GMP pharmaceutical experience preferred. Relocation assistance.
Requirements
- Degree in Biology, Chemistry, Biotechnology, or related field
- Advantageous experience in GMP pharmaceutical or API industry
- Ability to identify non-compliance and quality gaps
- Structured, precise, and well-organized working attitude
- Openness to new ideas and suggestions
- Agile, highly motivated, and dynamic drive
- Business fluent English
- Preferred good command of German
Tasks
- Review executed batch records and production documentation
- Examine test procedures, raw data, and logbooks
- Ensure documentation completeness to support batch releases
- Evaluate batch record comments with operations and QA managers
- Support deviations and investigations for review observations
- Collect and evaluate regular KPI data
- Write and revise SOPs within your area of expertise
- Collaborate with quality and operations functions
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- GMP
- API
Benefits
Bonuses & Incentives
- High performance compensation programs
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
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.
Not a perfect match?
- CH12 Lonza AG
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