Lonza
(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
Full-timeOn-siteJunior
Visp
New Job?Nejo!
The AI Job Search Engine
LOLonza
Operations Compliance Specialist(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Operations documentation and CAPA management at a large life sciences company, aligning SOPs with regulatory expectations. Pharmaceutical industry experience with GMP focus required. Relocation assistance.
Requirements
- Degree in Pharmacy, Engineering, or equivalent
- Pharmaceutical industry experience with GMP focus
- Excellent communication and detail-oriented style
- Knowledge of GMP and regulatory expectations
- Stakeholder collaboration and confident GMP representation
- Fluent English and basic German proficiency
Tasks
- Create and revise Operations SOPs and Work Instructions
- Conduct periodic reviews of operational documentation
- Align SOPs with current equipment and regulatory expectations
- Coordinate cross-functional reviews for timely implementation
- Manage General Operations CAPA actions and sustainability
- Drive on-time implementation of procedural and operational changes
- Provide evidence for CAPA effectiveness and inspection readiness
- Initiate and support Technical Change Requests
- Ensure changes are risk-assessed and properly justified
- Coordinate impact assessments on batch records and training
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GMP
Benefits
Bonuses & Incentives
- Performance-based compensation programs
Learning & Development
- Agile career opportunities
Startup Environment
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza 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?
- 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
QC Deviation & Investigation Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp
LOLonza
Operations Compliance Specialist(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Operations documentation and CAPA management at a large life sciences company, aligning SOPs with regulatory expectations. Pharmaceutical industry experience with GMP focus required. Relocation assistance.
Requirements
- Degree in Pharmacy, Engineering, or equivalent
- Pharmaceutical industry experience with GMP focus
- Excellent communication and detail-oriented style
- Knowledge of GMP and regulatory expectations
- Stakeholder collaboration and confident GMP representation
- Fluent English and basic German proficiency
Tasks
- Create and revise Operations SOPs and Work Instructions
- Conduct periodic reviews of operational documentation
- Align SOPs with current equipment and regulatory expectations
- Coordinate cross-functional reviews for timely implementation
- Manage General Operations CAPA actions and sustainability
- Drive on-time implementation of procedural and operational changes
- Provide evidence for CAPA effectiveness and inspection readiness
- Initiate and support Technical Change Requests
- Ensure changes are risk-assessed and properly justified
- Coordinate impact assessments on batch records and training
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GMP
Benefits
Bonuses & Incentives
- Performance-based compensation programs
Learning & Development
- Agile career opportunities
Startup Environment
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza 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
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?
- Lonza
(Senior) QA Operations Specialist, Small Molecules (Large Scale)(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
QC Deviation & Investigation Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp