Lonza
Team Lead Visual Inspection(m/w/x)
Full-timeOn-siteManagement
Visp
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Leading a QC monitoring team at a global pharmaceutical manufacturer, ensuring compliant processes for patient safety. 3-5 years GMP experience and team leadership skills required. Relocation assistance and agile career path.
Requirements
- University degree in life sciences or related scientific field
- 3–5 years of experience in GMP-regulated environment
- Experience leading, mentoring, or coordinating scientific or technical teams
- Strong understanding of regulatory standards, EU GMP Annex 1, and pharmacopoeias
- Experience with digital systems (MODA, LIMS, or DMS)
- Confident communication in English and German
- Structured, accountable, and solution-oriented manner
Tasks
- Lead and develop a high-performing monitoring team
- Ensure robust and compliant processes
- Support reliable manufacturing and patient safety
- Act as a key interface across functions
- Drive continuous improvement and operational excellence
- Coach and develop a team of scientists and specialists
- Allocate resources and prioritize workload
- Ensure timely delivery of operational and project activities
- Conduct performance reviews
- Support career development
- Foster an inclusive team culture
- Oversee daily monitoring operations
- Ensure accurate data collection, review, and reporting
- Review complex data trends and investigations
- Ensure scientific rigor and consistency
- Maintain GMP-compliant documentation
- Handle deviations, investigations, and preventive actions
- Collaborate with Operations, QA, Engineering, MSAT, and other stakeholders
Work Experience
- 3 - 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- MODA
- LIMS
- DMS
Benefits
Bonuses & Incentives
- Compensation programs recognizing leadership impact and performance
Other Benefits
- Relocation assistance
- Collaboration and accountability values
- Strong site visibility and influence
- Continuous improvement and innovation encouragement
Career Advancement
- Agile career path
- Opportunities to grow as scientific and people leader
Purpose-Driven Work
- Inclusive and ethical workplace
Diverse Work
- Dynamic, cross-functional role
Learning & Development
- Ongoing development opportunities in leadership, GMP, and digital systems
Informal Culture
- Supportive culture
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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Leading a QC monitoring team at a global pharmaceutical manufacturer, ensuring compliant processes for patient safety. 3-5 years GMP experience and team leadership skills required. Relocation assistance and agile career path.
Requirements
- University degree in life sciences or related scientific field
- 3–5 years of experience in GMP-regulated environment
- Experience leading, mentoring, or coordinating scientific or technical teams
- Strong understanding of regulatory standards, EU GMP Annex 1, and pharmacopoeias
- Experience with digital systems (MODA, LIMS, or DMS)
- Confident communication in English and German
- Structured, accountable, and solution-oriented manner
Tasks
- Lead and develop a high-performing monitoring team
- Ensure robust and compliant processes
- Support reliable manufacturing and patient safety
- Act as a key interface across functions
- Drive continuous improvement and operational excellence
- Coach and develop a team of scientists and specialists
- Allocate resources and prioritize workload
- Ensure timely delivery of operational and project activities
- Conduct performance reviews
- Support career development
- Foster an inclusive team culture
- Oversee daily monitoring operations
- Ensure accurate data collection, review, and reporting
- Review complex data trends and investigations
- Ensure scientific rigor and consistency
- Maintain GMP-compliant documentation
- Handle deviations, investigations, and preventive actions
- Collaborate with Operations, QA, Engineering, MSAT, and other stakeholders
Work Experience
- 3 - 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- MODA
- LIMS
- DMS
Benefits
Bonuses & Incentives
- Compensation programs recognizing leadership impact and performance
Other Benefits
- Relocation assistance
- Collaboration and accountability values
- Strong site visibility and influence
- Continuous improvement and innovation encouragement
Career Advancement
- Agile career path
- Opportunities to grow as scientific and people leader
Purpose-Driven Work
- Inclusive and ethical workplace
Diverse Work
- Dynamic, cross-functional role
Learning & Development
- Ongoing development opportunities in leadership, GMP, and digital systems
Informal Culture
- Supportive culture
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.
Not a perfect match?
- Lonza
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