Lonza
QC Raw Material Specialist(m/w/x)
Full-timeOn-siteExperienced
Visp
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Defining and leading compliance projects for pharmaceutical manufacturing QC II. 5+ years QA/QC/GMP and 3+ years project management experience required. Relocation assistance and tailored lifestyle benefits.
Requirements
- Lab-based education or equivalent scientific training
- 5+ years experience in QA, QC, or GMP environments
- 3+ years experience in project management
- Strong communication skills and ability to work with diverse stakeholders
- Experience collaborating with QC II/III, QA, customers, and authorities
Tasks
- Lead and define compliance projects within QC II
- Align teams to build and maintain one QC Visp compliance standard
- Support audits and inspections across end-to-end activities
- Strengthen inspection readiness by driving the right measures
- Provide expertise and training to QC II teams
- Own QC compliance KPIs and analyze trends
- Define strong actions based on KPI analysis
Work Experience
- 3 years
Education
- Vocational certification
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Other Benefits
- Tailored local benefits
- Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CH12 Lonza AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- ten23 health
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(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp
Defining and leading compliance projects for pharmaceutical manufacturing QC II. 5+ years QA/QC/GMP and 3+ years project management experience required. Relocation assistance and tailored lifestyle benefits.
Requirements
- Lab-based education or equivalent scientific training
- 5+ years experience in QA, QC, or GMP environments
- 3+ years experience in project management
- Strong communication skills and ability to work with diverse stakeholders
- Experience collaborating with QC II/III, QA, customers, and authorities
Tasks
- Lead and define compliance projects within QC II
- Align teams to build and maintain one QC Visp compliance standard
- Support audits and inspections across end-to-end activities
- Strengthen inspection readiness by driving the right measures
- Provide expertise and training to QC II teams
- Own QC compliance KPIs and analyze trends
- Define strong actions based on KPI analysis
Work Experience
- 3 years
Education
- Vocational certification
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Other Benefits
- Tailored local benefits
- Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CH12 Lonza AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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.
Not a perfect match?
- Lonza
QC Raw Material Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - ten23 health
Senior QMS & Compliance Expert(m/w/x)
Full-timeOn-siteSeniorVisp - ten23 health
QC Project Lead(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
QC Deviation & Investigation Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp