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(Senior) QA Qualification Specialist(m/w/x)
Description
In this role, you will be at the forefront of QA Qualification, coordinating project interests and driving new strategies. Your day-to-day responsibilities will involve compiling essential documents, supporting risk analyses, and ensuring compliance during audits.
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 Engineering, Chemistry, Biotechnology, or related field, or vocational education with strong relevant experience
- •Significant experience in the pharmaceutical industry, ideally in a QA role
- •Good understanding of applicable cGMP regulations
- •General knowledge of engineering and manufacturing processes
- •Ability to oversee project execution to identify non-compliance from quality standards
- •Fluent German (written and verbal) required; good English language skills advantageous
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Represent QA Qualification in project organizations
- •Coordinate QA interests during project phases
- •Drive implementation of new qualification strategies
- •Compile, review, and release Qualification Documents
- •Support and approve quality risk analyses
- •Perform assessments and approvals of technical change requests
- •Represent qualification topics during customer audits
- •Drive CAPA and Effectiveness Checks to completion
- •Ensure deviations are investigated and recorded
Languages
German – Business Fluent
English – Basic
Benefits
Bonuses & Incentives
- •Compensation programs recognizing high performance
Corporate Discounts
- •Numerous lifestyle benefits
- •Leisure benefits
Family Support
- •Family benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
- •Inclusive workplace
Purpose-Driven Work
- •Ethical workplace
Other Benefits
- •Relocation assistance
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
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(Senior) QA Qualification Specialist(m/w/x)
The AI Job Search Engine
Description
In this role, you will be at the forefront of QA Qualification, coordinating project interests and driving new strategies. Your day-to-day responsibilities will involve compiling essential documents, supporting risk analyses, and ensuring compliance during audits.
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 Engineering, Chemistry, Biotechnology, or related field, or vocational education with strong relevant experience
- •Significant experience in the pharmaceutical industry, ideally in a QA role
- •Good understanding of applicable cGMP regulations
- •General knowledge of engineering and manufacturing processes
- •Ability to oversee project execution to identify non-compliance from quality standards
- •Fluent German (written and verbal) required; good English language skills advantageous
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Represent QA Qualification in project organizations
- •Coordinate QA interests during project phases
- •Drive implementation of new qualification strategies
- •Compile, review, and release Qualification Documents
- •Support and approve quality risk analyses
- •Perform assessments and approvals of technical change requests
- •Represent qualification topics during customer audits
- •Drive CAPA and Effectiveness Checks to completion
- •Ensure deviations are investigated and recorded
Languages
German – Business Fluent
English – Basic
Benefits
Bonuses & Incentives
- •Compensation programs recognizing high performance
Corporate Discounts
- •Numerous lifestyle benefits
- •Leisure benefits
Family Support
- •Family benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
- •Inclusive workplace
Purpose-Driven Work
- •Ethical workplace
Other Benefits
- •Relocation assistance
About the Company
CH12 Lonza AG
Industry
Pharmaceuticals
Description
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
- CH12 Lonza AG
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