Lonza
Scientist - Quality Control, Environmental Monitoring(m/w/x)
Full-timeOn-siteExperienced
Visp
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LOLonza
(Senior) Scientist Quality Control, Environmental Monitoring(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Environmental monitoring and data evaluation in GMP-regulated pharmaceutical manufacturing. Two years of experience in a regulated environment required. Relocation assistance, agile career path.
Requirements
- Degree in life sciences or related scientific field
- Around two years of relevant experience in GMP-regulated environment
- Experience in environmental monitoring and/or microbiology is advantageous
- Strong digital skills, including Microsoft Office and documentation systems
- Knowledge of regulatory requirements, pharmacopoeias, and EU Annex 1 is ideal but not required
- Confident communication in English
- German skills are a plus
- Independent, proactive, detail-oriented, solution-focused mindset
Tasks
- Contribute to robust monitoring activities
- Evaluate complex data
- Improve processes
- Support compliance in GMP-regulated environment
- Collaborate with cross-functional partners
- Participate in inspections and continuous improvement
- Collect and evaluate monitoring data
- Summarize data using MODA, LIMS, and digital tools
- Document GMP-relevant activities
- Lead investigations of alert or action level excursions
- Drive root-cause investigations
- Align corrective actions with key stakeholders
- Create, review, and approve DMS documents
- Ensure document accuracy and compliance
- Enhance monitoring processes for data quality
- Improve monitoring efficiency and robustness
- Implement monitoring updates
- Manage MODA-related changes under change control
- Represent the team during inspections, audits, and customer visits
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Native
- German – Basic
Tools & Technologies
- Microsoft Office
Benefits
Other Benefits
- Performance and technical expertise recognition
- Relocation assistance
- Agile scientific career
- Dynamic GMP-regulated environment
- Collaboration and accountability values
- Regulatory interactions exposure
Purpose-Driven Work
- Inclusive and ethical workplace
- Ownership of impactful projects
Learning & Development
- Deepen expertise opportunities
- Learning encouragement
Startup Environment
- Cross-functional collaboration exposure
Informal Culture
- Supportive culture
Mentorship & Coaching
- Continuous improvement encouragement
Competitive Pay
- Competitive local benefits
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.
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LOLonza
(Senior) Scientist Quality Control, Environmental Monitoring(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Environmental monitoring and data evaluation in GMP-regulated pharmaceutical manufacturing. Two years of experience in a regulated environment required. Relocation assistance, agile career path.
Requirements
- Degree in life sciences or related scientific field
- Around two years of relevant experience in GMP-regulated environment
- Experience in environmental monitoring and/or microbiology is advantageous
- Strong digital skills, including Microsoft Office and documentation systems
- Knowledge of regulatory requirements, pharmacopoeias, and EU Annex 1 is ideal but not required
- Confident communication in English
- German skills are a plus
- Independent, proactive, detail-oriented, solution-focused mindset
Tasks
- Contribute to robust monitoring activities
- Evaluate complex data
- Improve processes
- Support compliance in GMP-regulated environment
- Collaborate with cross-functional partners
- Participate in inspections and continuous improvement
- Collect and evaluate monitoring data
- Summarize data using MODA, LIMS, and digital tools
- Document GMP-relevant activities
- Lead investigations of alert or action level excursions
- Drive root-cause investigations
- Align corrective actions with key stakeholders
- Create, review, and approve DMS documents
- Ensure document accuracy and compliance
- Enhance monitoring processes for data quality
- Improve monitoring efficiency and robustness
- Implement monitoring updates
- Manage MODA-related changes under change control
- Represent the team during inspections, audits, and customer visits
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Native
- German – Basic
Tools & Technologies
- Microsoft Office
Benefits
Other Benefits
- Performance and technical expertise recognition
- Relocation assistance
- Agile scientific career
- Dynamic GMP-regulated environment
- Collaboration and accountability values
- Regulatory interactions exposure
Purpose-Driven Work
- Inclusive and ethical workplace
- Ownership of impactful projects
Learning & Development
- Deepen expertise opportunities
- Learning encouragement
Startup Environment
- Cross-functional collaboration exposure
Informal Culture
- Supportive culture
Mentorship & Coaching
- Continuous improvement encouragement
Competitive Pay
- Competitive local benefits
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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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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