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Production support in pharmaceutical facilities, ensuring cGMP quality and deviation resolution. Professional experience in pharmaceutical production as operator/technician required. Relocation assistance for eligible candidates.
Requirements
- Completed chemical/biopharmaceutical education
- Professional experience in pharmaceutical production as an operator/production technician
- Safety-conscious work
- Knowledge of process engineering
- Fluent English with advantageous German language skills
- Willingness to work in shifts with flexible scheduling
Tasks
- Assist in various functions within production facilities
- Ensure compliance with safety regulations
- Adhere to cGMP quality requirements
- Recognize and interpret deviations
- Eliminate identified deviations
- Execute production steps, including recording and calculations
- Support training for new team members
Work Experience
- approx. 1 - 4 years
Education
- Vocational certification
Languages
- English – Business Fluent
- German – Basic
Benefits
Other Benefits
- Relocation assistance for eligible candidates
Not a perfect match?
- CH12 Lonza AGFull-timeOn-siteExperiencedVisp
- Lonza Group AG Basel
Operator Biotechnologist(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Senior Operator/Biotechnologist Ibex®(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Biotechnologe Buffer(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Biotechnologist Drug Product(m/w/x)
Full-timeOn-siteExperiencedVisp
Production support in pharmaceutical facilities, ensuring cGMP quality and deviation resolution. Professional experience in pharmaceutical production as operator/technician required. Relocation assistance for eligible candidates.
Requirements
- Completed chemical/biopharmaceutical education
- Professional experience in pharmaceutical production as an operator/production technician
- Safety-conscious work
- Knowledge of process engineering
- Fluent English with advantageous German language skills
- Willingness to work in shifts with flexible scheduling
Tasks
- Assist in various functions within production facilities
- Ensure compliance with safety regulations
- Adhere to cGMP quality requirements
- Recognize and interpret deviations
- Eliminate identified deviations
- Execute production steps, including recording and calculations
- Support training for new team members
Work Experience
- approx. 1 - 4 years
Education
- Vocational certification
Languages
- English – Business Fluent
- German – Basic
Benefits
Other Benefits
- Relocation assistance for eligible candidates
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.
Not a perfect match?
- CH12 Lonza AG
Operator / Biotechnologist(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza Group AG Basel
Operator Biotechnologist(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Senior Operator/Biotechnologist Ibex®(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Biotechnologe Buffer(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Biotechnologist Drug Product(m/w/x)
Full-timeOn-siteExperiencedVisp