1112 Celgene International SaRL
Technicien de maintenance process(m/w/x)
Full-timeWith HomeofficeSenior
Boudry
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BRBristol Myers Squibb
Intern - Manufacturing Science and Technology(m/w/x)
Boudry
Full-timeInternshipWith Home Office
Nejo AI Summary
Qualification and cleaning validation projects within a pharmaceutical MS&T team, applying DMAIC for process improvement. Master's or PhD student in Pharmaceuticals, with solid oral dosage forms knowledge, required. Exposure to global clinical trial context.
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
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
Education
- Currently in higher education
Languages
- French – Business Fluent
- English – Business Fluent
Tools & Technologies
- Minitab
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Bristol Myers Squibb and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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Intern - Manufacturing Science and Technology(m/w/x)
Boudry
Full-timeInternshipWith Home Office
Nejo AI Summary
Qualification and cleaning validation projects within a pharmaceutical MS&T team, applying DMAIC for process improvement. Master's or PhD student in Pharmaceuticals, with solid oral dosage forms knowledge, required. Exposure to global clinical trial context.
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
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
Education
- Currently in higher education
Languages
- French – Business Fluent
- English – Business Fluent
Tools & Technologies
- Minitab
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Bristol Myers Squibb and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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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