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(Senior) QA Qualification Specialist(m/w/x)
QA qualification for pharmaceutical projects, compiling and releasing documents at a global life sciences firm. Significant pharmaceutical industry experience with cGMP regulations understanding required. Project-based work, agile career path.
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
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
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
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
Not a perfect match?
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
- Lonza
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(Senior) QA Qualification Specialist(m/w/x)
QA qualification for pharmaceutical projects, compiling and releasing documents at a global life sciences firm. Significant pharmaceutical industry experience with cGMP regulations understanding required. Project-based work, agile career path.
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
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
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
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.
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