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CQV Engineer / Qualification & Validation Engineer(m/w/x)
Description
As a CQV Engineer, you will play a vital role in enhancing quality and efficiency by developing qualification documents, managing deviations, and coordinating projects with internal and external teams. Your contributions will directly impact operational excellence.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Graduation from a technical school or university degree
- •Proven experience in a regulated GMP environment
- •Strong proficiency in MS Office; familiarity with COMOS, DMS, Kneat, TrackWise, and SAP advantageous
- •Proficiency in written and spoken German and/or English
- •Independent and flexible work habits; excellent communication skills
- •Openness to new ideas; agility in thinking; proactivity in problem-solving
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Develop and maintain commissioning and qualification documents for new plants
- •Create PQs for critical systems
- •Provide ongoing SLC support post-implementation
- •Supervise and resolve deviations
- •Manage changes related to GEP and GMP
- •Implement CAPAs effectively
- •Coordinate efforts between internal teams and external service providers
- •Ensure seamless project execution
- •Present qualification documents during audits and inspections
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
Bonuses & Incentives
- •Compensation programs that recognize high performance
Corporate Discounts
- •Numerous lifestyle benefits
- •Leisure benefits
Family Support
- •Family benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
- •Inclusive workplace
Other Benefits
- •Relocation assistance
- LonzaFull-timeOn-siteExperiencedVisp
- CH12 Lonza AG
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CQV Engineer / Qualification & Validation Engineer(m/w/x)
The AI Job Search Engine
Description
As a CQV Engineer, you will play a vital role in enhancing quality and efficiency by developing qualification documents, managing deviations, and coordinating projects with internal and external teams. Your contributions will directly impact operational excellence.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Graduation from a technical school or university degree
- •Proven experience in a regulated GMP environment
- •Strong proficiency in MS Office; familiarity with COMOS, DMS, Kneat, TrackWise, and SAP advantageous
- •Proficiency in written and spoken German and/or English
- •Independent and flexible work habits; excellent communication skills
- •Openness to new ideas; agility in thinking; proactivity in problem-solving
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Develop and maintain commissioning and qualification documents for new plants
- •Create PQs for critical systems
- •Provide ongoing SLC support post-implementation
- •Supervise and resolve deviations
- •Manage changes related to GEP and GMP
- •Implement CAPAs effectively
- •Coordinate efforts between internal teams and external service providers
- •Ensure seamless project execution
- •Present qualification documents during audits and inspections
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
Bonuses & Incentives
- •Compensation programs that recognize high performance
Corporate Discounts
- •Numerous lifestyle benefits
- •Leisure benefits
Family Support
- •Family benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
- •Inclusive workplace
Other Benefits
- •Relocation assistance
About the Company
CH12 Lonza AG
Industry
Healthcare
Description
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
- Lonza
Qualification CQV Engineer(m/w/x)
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Qualifizierungsspezialist CQV(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - ten23 health
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