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(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
Description
You will ensure manufacturing excellence by overseeing GMP compliance and batch documentation. Your day-to-day involves managing quality agreements and audits to meet high industry standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Chemistry, Biochemistry, Pharmacy, or similar
- •Initial industrial experience, GMP knowledge, or manufacturing experience
- •Strong German and English communication skills
- •Ownership, structured working, and team orientation
- •Accurate interpretation of regulatory and business requirements
- •Proficiency in MS Office and pharmaceutical IT systems
- •Quick comprehension and strong organizational abilities
Education
Tasks
- •Ensure manufacturing follows health authority registrations
- •Monitor compliance with international customer quality agreements
- •Maintain transparent relationships to meet quality expectations
- •Review batch manufacturing documentation for GMP compliance
- •Assess and approve deviations and change requests
- •Manage CAPA actions and quality risk assessments
- •Prepare detailed Quality Review Reports
- •Conduct internal audits and support regulatory inspections
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
Bonuses & Incentives
- •Performance-based compensation programs
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Other Benefits
- •Relocation assistance
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
- Lonza
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(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
The AI Job Search Engine
Description
You will ensure manufacturing excellence by overseeing GMP compliance and batch documentation. Your day-to-day involves managing quality agreements and audits to meet high industry standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Chemistry, Biochemistry, Pharmacy, or similar
- •Initial industrial experience, GMP knowledge, or manufacturing experience
- •Strong German and English communication skills
- •Ownership, structured working, and team orientation
- •Accurate interpretation of regulatory and business requirements
- •Proficiency in MS Office and pharmaceutical IT systems
- •Quick comprehension and strong organizational abilities
Education
Tasks
- •Ensure manufacturing follows health authority registrations
- •Monitor compliance with international customer quality agreements
- •Maintain transparent relationships to meet quality expectations
- •Review batch manufacturing documentation for GMP compliance
- •Assess and approve deviations and change requests
- •Manage CAPA actions and quality risk assessments
- •Prepare detailed Quality Review Reports
- •Conduct internal audits and support regulatory inspections
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
Bonuses & Incentives
- •Performance-based compensation programs
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Other Benefits
- •Relocation assistance
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
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