Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Full-timeOn-siteSenior
Visp
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CHCH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Managing GMP compliance for API production and contract manufacturing in life sciences. Batch release expertise and GMP experience in biopharma preferred. International project collaboration, cross-functional team advising.
Requirements
- University degree in Life Sciences (Microbiology, Biotechnology, Chemistry)
- First experience in GMP environment, preferably in biopharmaceutical industry
- Strong communication skills and experience working with stakeholders from different departments
- Experience with TrackWise, SAP, LIMS, and DMS
- Batch release expertise
- Fluency in English and German (written and verbal)
Tasks
- Ensure API production complies with Good Manufacturing Practice (GMP)
- Support contract manufacturing processes
- Advise development, production, and analytical teams on GMP aspects
- Check manufacturing documentation for conformity
- Process change controls
- Review and approve deviations and out-of-specification (OOS) results
- Act as the quality contact for clients
- Present during GMP audits
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- TrackWise
- SAP
- LIMS
- DMS
Benefits
Bonuses & Incentives
- Compensation programs that recognize high performance
Startup Environment
- Agile career and dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
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
Senior QA Specialist, QA Project Management(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Managing GMP compliance for API production and contract manufacturing in life sciences. Batch release expertise and GMP experience in biopharma preferred. International project collaboration, cross-functional team advising.
Requirements
- University degree in Life Sciences (Microbiology, Biotechnology, Chemistry)
- First experience in GMP environment, preferably in biopharmaceutical industry
- Strong communication skills and experience working with stakeholders from different departments
- Experience with TrackWise, SAP, LIMS, and DMS
- Batch release expertise
- Fluency in English and German (written and verbal)
Tasks
- Ensure API production complies with Good Manufacturing Practice (GMP)
- Support contract manufacturing processes
- Advise development, production, and analytical teams on GMP aspects
- Check manufacturing documentation for conformity
- Process change controls
- Review and approve deviations and out-of-specification (OOS) results
- Act as the quality contact for clients
- Present during GMP audits
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- TrackWise
- SAP
- LIMS
- DMS
Benefits
Bonuses & Incentives
- Compensation programs that recognize high performance
Startup Environment
- Agile career and dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
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
Healthcare
Description
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
Not a perfect match?
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