Lonza
Senior QA Specialist, QA Operations(m/w/x)
Full-timeOn-siteSenior
Visp
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Quality oversight for GMP manufacturing, tech transfer, and commissioning at a global life sciences company. Significant pharmaceutical quality experience required. Work in a 5-person QA team with rotating shift times.
Requirements
- Bachelor of Science in Life Science or related field
- Significant pharmaceutical quality experience
- Work experience in QA, Production, or Engineering in pharmaceutical industries and cGMP environment
- QA experience in tech transfer preferred
- Excellent knowledge of computer systems (e.g. TW, SAP, etc.)
- Excellent knowledge of quality tools such as risk based approaches (e.g. FMEA)
- Fluency in English
Tasks
- Manage QA activities with QC, Engineering, and Manufacturing
- Ensure quality oversight for project delivery
- Handle QA operations during commissioning and tech transfer
- Assess and manage quality impacts during GMP manufacturing
- Plan and coordinate future activities with other departments
- Support daily Quality Assurance activities per SOPs
- Review GMP records for compliance with cGMP
- Make real-time decisions on process events
- Participate in walkthroughs and audits
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Fluent
Tools & Technologies
- TW
- SAP
- FMEA
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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Quality oversight for GMP manufacturing, tech transfer, and commissioning at a global life sciences company. Significant pharmaceutical quality experience required. Work in a 5-person QA team with rotating shift times.
Requirements
- Bachelor of Science in Life Science or related field
- Significant pharmaceutical quality experience
- Work experience in QA, Production, or Engineering in pharmaceutical industries and cGMP environment
- QA experience in tech transfer preferred
- Excellent knowledge of computer systems (e.g. TW, SAP, etc.)
- Excellent knowledge of quality tools such as risk based approaches (e.g. FMEA)
- Fluency in English
Tasks
- Manage QA activities with QC, Engineering, and Manufacturing
- Ensure quality oversight for project delivery
- Handle QA operations during commissioning and tech transfer
- Assess and manage quality impacts during GMP manufacturing
- Plan and coordinate future activities with other departments
- Support daily Quality Assurance activities per SOPs
- Review GMP records for compliance with cGMP
- Make real-time decisions on process events
- Participate in walkthroughs and audits
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Fluent
Tools & Technologies
- TW
- SAP
- FMEA
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
Science
Description
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Not a perfect match?
- Lonza
Senior QA Specialist, QA Operations(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist, DPS (Drug Product Services)(m/w/x)
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Senior QA Specialist/QA Project Manager(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist, Supplier Management(m/w/x)
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