CH12 Lonza AG
Senior QA Specialist(m/w/x)
Full-timeOn-siteSenior
Visp
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LOLonza
Senior QA Specialist - Product Quality Review(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Training Process Validation Specialists on product quality oversight and refining validation practices at a life sciences firm. Fluent English and German skills, plus GMP manufacturing experience required. Performance-based compensation programs.
Requirements
- Degree in Chemistry, Biotechnology, or related field
- Fluent English and German skills
- Proficiency in writing scientific reports
- Experience in GMP manufacturing
- Excellent communication skills
- Proactive improvement of business processes
Tasks
- Train Process Validation Specialists on Product Quality Reviews
- Share expertise within the validation team
- Develop and refine validation practices
- Ensure project compliance with specific company SOPs
- Prepare and approve monthly PQR Newsletters
- Maintain the PQR status overview list
- Review and approve process-specific PQRs
- Evaluate change requests, deviations, and SOPs
- Represent PQR and CPV during customer audits
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- GMP
Benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Bonuses & Incentives
- Performance-based compensation programs
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
Senior QA Specialist - Product Quality Review(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Training Process Validation Specialists on product quality oversight and refining validation practices at a life sciences firm. Fluent English and German skills, plus GMP manufacturing experience required. Performance-based compensation programs.
Requirements
- Degree in Chemistry, Biotechnology, or related field
- Fluent English and German skills
- Proficiency in writing scientific reports
- Experience in GMP manufacturing
- Excellent communication skills
- Proactive improvement of business processes
Tasks
- Train Process Validation Specialists on Product Quality Reviews
- Share expertise within the validation team
- Develop and refine validation practices
- Ensure project compliance with specific company SOPs
- Prepare and approve monthly PQR Newsletters
- Maintain the PQR status overview list
- Review and approve process-specific PQRs
- Evaluate change requests, deviations, and SOPs
- Represent PQR and CPV during customer audits
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- GMP
Benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Bonuses & Incentives
- Performance-based compensation programs
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?
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