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Internship - cleaning validation(m/w/x)
Description
In this internship, you will play a key role in defining and executing cleaning validation strategies for GMP manufacturing equipment, ensuring the safety of new biological entities for clinical trials. Your day-to-day responsibilities will involve designing protocols, analyzing data, and collaborating on comprehensive reports.
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Requirements
- •Master/engineer student in Biotechnology or related fields
- •High motivation
- •Autonomy
- •Previous experience in Up Stream Process/Down Stream Process is a plus
- •Good written and oral knowledge in English
- •French is a plus
Education
Tasks
- •Contribute to cleaning validation strategy definition
- •Confirm cleaning validation strategy according to standards
- •Design protocols that meet regulatory requirements
- •Execute parts of the cleaning validation study
- •Ensure compliance with GMP during validation
- •Analyze data collected during the study
- •Write a report summarizing methodology and results
- •Collaborate on recommendations for the final report
Languages
English – Business Fluent
French – Basic
- SUSONITYFull-timeInternshipOn-siteCorsier-sur-Vevey
- SUSONITY
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Internship - cleaning validation(m/w/x)
The AI Job Search Engine
Description
In this internship, you will play a key role in defining and executing cleaning validation strategies for GMP manufacturing equipment, ensuring the safety of new biological entities for clinical trials. Your day-to-day responsibilities will involve designing protocols, analyzing data, and collaborating on comprehensive reports.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Master/engineer student in Biotechnology or related fields
- •High motivation
- •Autonomy
- •Previous experience in Up Stream Process/Down Stream Process is a plus
- •Good written and oral knowledge in English
- •French is a plus
Education
Tasks
- •Contribute to cleaning validation strategy definition
- •Confirm cleaning validation strategy according to standards
- •Design protocols that meet regulatory requirements
- •Execute parts of the cleaning validation study
- •Ensure compliance with GMP during validation
- •Analyze data collected during the study
- •Write a report summarizing methodology and results
- •Collaborate on recommendations for the final report
Languages
English – Business Fluent
French – Basic
About the Company
SUSONITY
Industry
Healthcare
Description
Das Unternehmen entwickelt Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit.
- SUSONITY
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