Your personal AI career agent
(Senior) QA Specialist, Material Management(m/w/x)
Independent QA review and approval of QC documentation for pharmaceutical manufacturing. GxP industry experience and quality systems knowledge required. Relocation assistance provided.
Requirements
- Academic degree in Life Sciences, Pharmacy, or Chemistry
- Proven QA/QC experience in regulated (GxP) industry
- Solid knowledge of quality systems (deviations, change controls, CAPAs, investigations)
- Experience reviewing and approving QC documentation
- Experience with ERP systems (SAP) and quality master data is advantageous
- Strong communication skills and attention to detail
- Ability to collaborate effectively across functions
- Good team player
- Willingness to learn and grow
- Fluent English skills
- German language skills are an advantage
Tasks
- Provide independent QA review and approval
- Ensure documentation and data meet standards
- Support cross-functional quality alignment
- Serve as QA point of contact for quality-related questions
- Review and approve QC documentation
- Prepare and approve risk assessments
- Review and approve product statements
- Approve SAP material workflows
- Approve quality-relevant master data
- Assess and review quality records
- Approve deviations, change controls, CAPAs, investigations
- Conduct effectiveness checks
- Ensure compliance with SOPs and regulations
- Collaborate with Procurement, MSAT, QA Supplier Management, QC, and Regulatory Affairs
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Fluent
Tools & Technologies
- Trackwise
- SAP
Benefits
Other Benefits
- Relocation assistance
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
Not a perfect match?
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
- CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Senior QA Specialist, QA Operations(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist, Supplier Management(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Full-timeOn-siteSeniorVisp
(Senior) QA Specialist, Material Management(m/w/x)
Independent QA review and approval of QC documentation for pharmaceutical manufacturing. GxP industry experience and quality systems knowledge required. Relocation assistance provided.
Requirements
- Academic degree in Life Sciences, Pharmacy, or Chemistry
- Proven QA/QC experience in regulated (GxP) industry
- Solid knowledge of quality systems (deviations, change controls, CAPAs, investigations)
- Experience reviewing and approving QC documentation
- Experience with ERP systems (SAP) and quality master data is advantageous
- Strong communication skills and attention to detail
- Ability to collaborate effectively across functions
- Good team player
- Willingness to learn and grow
- Fluent English skills
- German language skills are an advantage
Tasks
- Provide independent QA review and approval
- Ensure documentation and data meet standards
- Support cross-functional quality alignment
- Serve as QA point of contact for quality-related questions
- Review and approve QC documentation
- Prepare and approve risk assessments
- Review and approve product statements
- Approve SAP material workflows
- Approve quality-relevant master data
- Assess and review quality records
- Approve deviations, change controls, CAPAs, investigations
- Conduct effectiveness checks
- Ensure compliance with SOPs and regulations
- Collaborate with Procurement, MSAT, QA Supplier Management, QC, and Regulatory Affairs
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Fluent
Tools & Technologies
- Trackwise
- SAP
Benefits
Other Benefits
- Relocation assistance
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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
Senior QA Specialist(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Senior QA Specialist, QA Operations(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist, Supplier Management(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Full-timeOn-siteSeniorVisp