CH12 Lonza AG
Manager Manufacturing(m/w/x)
Full-timeOn-siteManagement
Visp
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LOLonza
Manufacturing Manager Operations USP(m/w/x)
Visp
Full-timeOn-siteManagement
Nejo AI Summary
Overseeing production of commercial, clinical, and toxicology supplies at a global life sciences firm, leading a 10-person technical team. GMP compliance experience and team leadership background required. Regular interaction with customers and regulatory auditors.
Requirements
- Bachelor's degree or higher
- Experience in Manufacturing or related fields
- Background in team management
- Maturity, confidence, and emotional intelligence
- Agile relationship management skills
- Fluent English and German
Tasks
- Manufacture commercial, clinical, and toxicology supplies
- Ensure compliance with GMP regulations
- Lead a technical team of ten contributors
- Coach and train employees to improve performance
- Interface with customers and regulatory auditors
- Lead facility tours for auditors
- Remediate all audit observations
- Allocate resources to achieve production goals
- Review and approve QMS investigations
- Manage production schedules with customers
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- GMP
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
Manufacturing Manager Operations USP(m/w/x)
Visp
Full-timeOn-siteManagement
Nejo AI Summary
Overseeing production of commercial, clinical, and toxicology supplies at a global life sciences firm, leading a 10-person technical team. GMP compliance experience and team leadership background required. Regular interaction with customers and regulatory auditors.
Requirements
- Bachelor's degree or higher
- Experience in Manufacturing or related fields
- Background in team management
- Maturity, confidence, and emotional intelligence
- Agile relationship management skills
- Fluent English and German
Tasks
- Manufacture commercial, clinical, and toxicology supplies
- Ensure compliance with GMP regulations
- Lead a technical team of ten contributors
- Coach and train employees to improve performance
- Interface with customers and regulatory auditors
- Lead facility tours for auditors
- Remediate all audit observations
- Allocate resources to achieve production goals
- Review and approve QMS investigations
- Manage production schedules with customers
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- GMP
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.
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