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Operator Biotechnologist(m/w/x)
Description
As an Operator Biotechnologist, you will be at the forefront of manufacturing, ensuring that each batch is produced safely and meets quality standards. This role involves inspecting products, supporting the team, and maintaining equipment to deliver safe, sterile injections to patients.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Experience in a GMP-regulated environment
- •Fluency in English or German
- •Familiarity with GMP requirements and quality procedures
- •Strong team orientation
- •Excellent communication skills
- •Structured and organized working approach
Work Experience
approx. 1 - 4 years
Tasks
- •Execute manufacturing activities in the Drug Product area
- •Perform manual visual inspections of liquid and lyophilized vials
- •Identify and remove defective units from production
- •Ensure final products are free from defects
- •Provide technical and procedural support to the manufacturing team
- •Manufacture each batch safely and on schedule
- •Comply with batch instructions and quality requirements
- •Prepare production documentation accurately and on time
- •Operate, set up, and clean production equipment and premises
Languages
English – Business Fluent
German – Basic
Benefits
Flexible Working
- •Flexible hours
Other Benefits
- •Relocation assistance
Career Advancement
- •Agile career
Startup Environment
- •Dynamic working culture
Informal Culture
- •Inclusive workplace
Purpose-Driven Work
- •Ethical workplace
- CH12 Lonza AGFull-timeOn-siteExperiencedVisp
- CH12 Lonza AG
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Operator Biotechnologist(m/w/x)
The AI Job Search Engine
Description
As an Operator Biotechnologist, you will be at the forefront of manufacturing, ensuring that each batch is produced safely and meets quality standards. This role involves inspecting products, supporting the team, and maintaining equipment to deliver safe, sterile injections to patients.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Experience in a GMP-regulated environment
- •Fluency in English or German
- •Familiarity with GMP requirements and quality procedures
- •Strong team orientation
- •Excellent communication skills
- •Structured and organized working approach
Work Experience
approx. 1 - 4 years
Tasks
- •Execute manufacturing activities in the Drug Product area
- •Perform manual visual inspections of liquid and lyophilized vials
- •Identify and remove defective units from production
- •Ensure final products are free from defects
- •Provide technical and procedural support to the manufacturing team
- •Manufacture each batch safely and on schedule
- •Comply with batch instructions and quality requirements
- •Prepare production documentation accurately and on time
- •Operate, set up, and clean production equipment and premises
Languages
English – Business Fluent
German – Basic
Benefits
Flexible Working
- •Flexible hours
Other Benefits
- •Relocation assistance
Career Advancement
- •Agile career
Startup Environment
- •Dynamic working culture
Informal Culture
- •Inclusive workplace
Purpose-Driven Work
- •Ethical workplace
About the Company
Lonza Group AG Basel
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein weltweit führendes Unternehmen im Bereich Life Sciences, das innovative Lösungen für komplexe Probleme entwickelt.
- CH12 Lonza AG
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