The AI Job Search Engine
Senior QA Specialist - Product Quality Review(m/w/x)
Description
You will drive product excellence by overseeing quality reviews and compliance. From mentoring specialists to managing audits, your work ensures that validation standards remain world-class.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
Work Experience
approx. 4 - 6 years
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
Tools & Technologies
Languages
English – Business Fluent
German – Business Fluent
Benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Bonuses & Incentives
- •Performance-based compensation programs
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
- Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist - Qualification/Validation/EM (Environmental Monitoring)(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp
Senior QA Specialist - Product Quality Review(m/w/x)
The AI Job Search Engine
Description
You will drive product excellence by overseeing quality reviews and compliance. From mentoring specialists to managing audits, your work ensures that validation standards remain world-class.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
Work Experience
approx. 4 - 6 years
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
Tools & Technologies
Languages
English – Business Fluent
German – Business Fluent
Benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Bonuses & Incentives
- •Performance-based compensation programs
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.
- CH12 Lonza AG
Senior QA Specialist(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist - Qualification/Validation/EM (Environmental Monitoring)(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp