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Intern - Manufacturing Science and Technology(m/w/x)
Description
In this intern role, you will engage in various qualification and cleaning validation projects while collaborating with the MS&T team and other departments. Your day-to-day responsibilities will involve troubleshooting production operations and supporting process improvements through data analysis.
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Requirements
- •Master's or PhD student in Pharmaceuticals
- •Good understanding of GMP rules and Pharmaceutical regulations
- •Good knowledge of solid oral dosage forms manufacturing and/or packaging processes
- •Good understanding of chemical and physical analytical methodologies in Pharmaceuticals
- •Basic knowledge of Failure Mode and Effects Analysis methodology
- •Awareness of problem-solving methodologies
- •Basic knowledge of statistical tools (Minitab or equivalent)
- •Team player and agility
- •"Think out of the box" philosophy for improvement projects
- •Fluency in French and English
Education
Tasks
- •Support qualification and cleaning validation projects
- •Assist in troubleshooting operations on production sites
- •Collaborate with MS&T team members and other operational departments
- •Collect and analyze data for process improvement using DMAIC methodology
- •Contribute to updates and improvements in Visual Management for the Validation & Robustness department
Tools & Technologies
Languages
French – Business Fluent
English – Business Fluent
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Intern - Manufacturing Science and Technology(m/w/x)
The AI Job Search Engine
Description
In this intern role, you will engage in various qualification and cleaning validation projects while collaborating with the MS&T team and other departments. Your day-to-day responsibilities will involve troubleshooting production operations and supporting process improvements through data analysis.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Master's or PhD student in Pharmaceuticals
- •Good understanding of GMP rules and Pharmaceutical regulations
- •Good knowledge of solid oral dosage forms manufacturing and/or packaging processes
- •Good understanding of chemical and physical analytical methodologies in Pharmaceuticals
- •Basic knowledge of Failure Mode and Effects Analysis methodology
- •Awareness of problem-solving methodologies
- •Basic knowledge of statistical tools (Minitab or equivalent)
- •Team player and agility
- •"Think out of the box" philosophy for improvement projects
- •Fluency in French and English
Education
Tasks
- •Support qualification and cleaning validation projects
- •Assist in troubleshooting operations on production sites
- •Collaborate with MS&T team members and other operational departments
- •Collect and analyze data for process improvement using DMAIC methodology
- •Contribute to updates and improvements in Visual Management for the Validation & Robustness department
Tools & Technologies
Languages
French – Business Fluent
English – Business Fluent
About the Company
Bristol Myers Squibb
Industry
Pharmaceuticals
Description
The company is dedicated to transforming patients’ lives through science and promotes global participation in clinical trials.
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