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Owning investigations and CAPA implementation for critical deviations in sterile manufacturing processes at a global life sciences firm. One year sterile manufacturing experience with investigation/deviation management required. Relocation assistance provided.
Requirements
- Bachelor's or Master's Degree in Pharmaceutical Technology, Chemistry, Pharmacy, or equivalent work experience
- At least one year of experience in Sterile Manufacturing in operations and/or QC/QA
- Previous experience with investigation/deviation management in TW and CAPA definition
- Proficiency in English; German is an advantage
- Familiarity with GMP requirements, quality procedures, and SOP execution
- Good interpersonal skills with various interfaces within the organization and shopfloor
- Structured, focused, proactive, and well-organized working demeanor
- High motivation and collaboration focus; oriented towards finding solutions and driven by science
Tasks
- Drive optimization projects for manufacturing processes
- Own investigations and critical deviations
- Assist in decision-making on production issues
- Implement process changes and CAPAs
- Conduct CAPA efficiency checks within required timelines
- Utilize GMP systems like Trackwise, SAP, and MES
- Perform retraining and awareness sessions as needed
Work Experience
- 1 year
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Numerous lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Other Benefits
- Relocation assistance
Not a perfect match?
- CH12 Lonza AGFull-timeOn-siteNot specifiedVisp
- Lonza
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Owning investigations and CAPA implementation for critical deviations in sterile manufacturing processes at a global life sciences firm. One year sterile manufacturing experience with investigation/deviation management required. Relocation assistance provided.
Requirements
- Bachelor's or Master's Degree in Pharmaceutical Technology, Chemistry, Pharmacy, or equivalent work experience
- At least one year of experience in Sterile Manufacturing in operations and/or QC/QA
- Previous experience with investigation/deviation management in TW and CAPA definition
- Proficiency in English; German is an advantage
- Familiarity with GMP requirements, quality procedures, and SOP execution
- Good interpersonal skills with various interfaces within the organization and shopfloor
- Structured, focused, proactive, and well-organized working demeanor
- High motivation and collaboration focus; oriented towards finding solutions and driven by science
Tasks
- Drive optimization projects for manufacturing processes
- Own investigations and critical deviations
- Assist in decision-making on production issues
- Implement process changes and CAPAs
- Conduct CAPA efficiency checks within required timelines
- Utilize GMP systems like Trackwise, SAP, and MES
- Perform retraining and awareness sessions as needed
Work Experience
- 1 year
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Numerous lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Other Benefits
- Relocation assistance
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.
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