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(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
QA operations for high-volume pharmaceutical production at a global life sciences company. Degree in Chemistry, Biochemistry, or Pharmacy with initial industrial experience required. Relocation assistance provided.
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
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
Education
- Vocational certification
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- MS Office
- Documentum
- LIMS
- TrackWise
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
Not a perfect match?
- LonzaFull-timeOn-siteJuniorVisp
- Lonza
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(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
QA operations for high-volume pharmaceutical production at a global life sciences company. Degree in Chemistry, Biochemistry, or Pharmacy with initial industrial experience required. Relocation assistance provided.
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
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
Education
- Vocational certification
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- MS Office
- Documentum
- LIMS
- TrackWise
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.
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