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QC Deviation & Investigation Specialist(m/w/x)
Leading deviation management and document approval (DMS) in life sciences, executing tasks within LIMS. MSc or PhD in scientific/technical field required, QMS or TrackWise experience essential. High performance compensation programs, lifestyle and family benefits offered.
Requirements
- MSc or PhD in scientific or technical field
- Experience with Quality Management Systems or TrackWise
- GMP knowledge as an advantage
- Strong problem‑solving ability and proactive mindset
- Excellent analytical and technical understanding
- Business‑fluent English and German skills
Tasks
- Lead deviation management in your assigned area
- Drive corrective and preventive actions
- Create, review, and approve DMS documents
- Support continuous improvement for QC 24/7 processes
- Execute essential tasks within the LIMS system
- Implement operational changes to meet business needs
- Act as the primary contact for compliance topics
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- TrackWise
- Quality Management Systems
- GMP
Benefits
Bonuses & Incentives
- High performance compensation programs
Family Support
- Lifestyle, family, and leisure benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
Not a perfect match?
- CH12 Lonza AGFull-timeOn-siteNot specifiedVisp
- CH12 Lonza AG
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QC Deviation & Investigation Specialist(m/w/x)
Leading deviation management and document approval (DMS) in life sciences, executing tasks within LIMS. MSc or PhD in scientific/technical field required, QMS or TrackWise experience essential. High performance compensation programs, lifestyle and family benefits offered.
Requirements
- MSc or PhD in scientific or technical field
- Experience with Quality Management Systems or TrackWise
- GMP knowledge as an advantage
- Strong problem‑solving ability and proactive mindset
- Excellent analytical and technical understanding
- Business‑fluent English and German skills
Tasks
- Lead deviation management in your assigned area
- Drive corrective and preventive actions
- Create, review, and approve DMS documents
- Support continuous improvement for QC 24/7 processes
- Execute essential tasks within the LIMS system
- Implement operational changes to meet business needs
- Act as the primary contact for compliance topics
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- TrackWise
- Quality Management Systems
- GMP
Benefits
Bonuses & Incentives
- High performance compensation programs
Family Support
- Lifestyle, family, and leisure benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work 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.
Not a perfect match?
- CH12 Lonza AG
Deviation Specialist(m/w/x)
Full-timeOn-siteNot specifiedVisp - CH12 Lonza AG
Investigation Specialist(m/w/x)
Full-timeOn-siteJuniorVisp - CH12 Lonza AG
GMP Ops Support(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior Deviation Specialist(m/w/x)
Full-timeOn-siteSeniorVisp