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Senior QA Specialist, QA Operations(m/w/x)
Description
In this role, you will oversee quality assurance operations for a growth project, ensuring compliance and timely delivery by collaborating with various departments and making informed decisions on the manufacturing floor.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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)
Education
Work Experience
approx. 4 - 6 years
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
Tools & Technologies
Languages
English – Business Fluent
Benefits
Other Benefits
- •Lifestyle benefits
- •Relocation assistance
Family Support
- •Family benefits
Corporate Discounts
- •Leisure benefits
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
- CH12 Lonza AG
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Senior QA Specialist, QA Operations(m/w/x)
The AI Job Search Engine
Description
In this role, you will oversee quality assurance operations for a growth project, ensuring compliance and timely delivery by collaborating with various departments and making informed decisions on the manufacturing floor.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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)
Education
Work Experience
approx. 4 - 6 years
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
Tools & Technologies
Languages
English – Business Fluent
Benefits
Other Benefits
- •Lifestyle benefits
- •Relocation assistance
Family Support
- •Family benefits
Corporate Discounts
- •Leisure benefits
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 - CH12 Lonza AG
Senior QA Specialist, QA Project Management(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 - Lonza
Senior QA Automation Specialist(m/w/x)
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