CH12 Lonza AG
Senior QA Specialist(m/w/x)
Full-timeOn-siteSenior
Visp
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Overseeing quality operations for commissioning and qualification at global life sciences firm, coordinating with QC, Engineering, and Manufacturing. Significant experience in pharmaceutical quality required; tech transfer experience preferred. Relocation assistance available.
Requirements
- Academic degree in Life Sciences or related field
- Significant experience in pharmaceutical Quality area
- Work experience in Quality Assurance, Production or Engineering in pharmaceutical industries and cGMP regulated environment
- Preferred QA experience in tech transfer
- Excellent knowledge of computer systems and quality tools such as risk based approaches
- Fluent English (written and verbal)
Tasks
- Manage QA operations during commissioning and qualification
- Assess and manage tasks impacting quality during GMP manufacturing
- Plan future activities and coordinate with QC, Engineering, and Manufacturing
- Support daily Quality Assurance activities per approved SOPs and policies
- Review GMP records for compliance with cGMP procedures
- Make real-time decisions on process events based on SOPs and policies
- Participate in walkthroughs and audits/inspections
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- TW
- SAP
Benefits
Other Benefits
- Lifestyle benefits
- Relocation assistance
Family Support
- Family benefits
Corporate Discounts
- Leisure benefits
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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Overseeing quality operations for commissioning and qualification at global life sciences firm, coordinating with QC, Engineering, and Manufacturing. Significant experience in pharmaceutical quality required; tech transfer experience preferred. Relocation assistance available.
Requirements
- Academic degree in Life Sciences or related field
- Significant experience in pharmaceutical Quality area
- Work experience in Quality Assurance, Production or Engineering in pharmaceutical industries and cGMP regulated environment
- Preferred QA experience in tech transfer
- Excellent knowledge of computer systems and quality tools such as risk based approaches
- Fluent English (written and verbal)
Tasks
- Manage QA operations during commissioning and qualification
- Assess and manage tasks impacting quality during GMP manufacturing
- Plan future activities and coordinate with QC, Engineering, and Manufacturing
- Support daily Quality Assurance activities per approved SOPs and policies
- Review GMP records for compliance with cGMP procedures
- Make real-time decisions on process events based on SOPs and policies
- Participate in walkthroughs and audits/inspections
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- TW
- SAP
Benefits
Other Benefits
- Lifestyle benefits
- Relocation assistance
Family Support
- Family benefits
Corporate Discounts
- Leisure benefits
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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