Intern - Manufacturing Science and Technology
Bristol-Myers Squibb
Intern - Manufacturing Science and Technology
Job Description
Master's or PhD student with a background 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 applied in the Pharmaceutical Industry 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 Fluent in French and English Support different Qualification and cleaning validation projects according to business needs, Support troubleshooting operations on production sites, Collaborates closely with MS&T team members and with other operational departments located in different areas Provides support for processes improvement (data collection, data trending, data analysis) with DMAIC methodology Contributes to Visual Management updates and improvements for Validation & Robustness department Supporting People with Disabilities
About the Role/Company
- Supporting People with Disabilities
Key Responsibilities
- Support different Qualification and cleaning validation projects according to business needs
- Support troubleshooting operations on production sites
- Collaborates closely with MS&T team members and with other operational departments located in different areas
- Provides support for processes improvement (data collection, data trending, data analysis) with DMAIC methodology
- Contributes to Visual Management updates and improvements for Validation & Robustness department
Required Qualifications
- Master's or PhD student with a background 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 applied in the Pharmaceutical Industry
- Basic knowledge of Failure Mode and Effects Analysis methodology
- Awareness of problem-solving methodologies
- Basic knowledge of statistical tools (Minitab or equivalent)
- Fluent in French and English
Skills Required
- Team player and agility
- "Think out of the box" philosophy for improvement projects
Locations
- Boudry, Switzerland
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
40,000 - 60,000 CHF / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Team player and agilityintermediate
- "Think out of the box" philosophy for improvement projectsintermediate
Required Qualifications
- Master's or PhD student with a background in Pharmaceuticals (experience)
- Good understanding of GMP rules and Pharmaceutical regulations (experience)
- Good knowledge of solid oral dosage forms manufacturing and/or packaging processes (experience)
- Good understanding of chemical and physical analytical methodologies applied in the Pharmaceutical Industry (experience)
- Basic knowledge of Failure Mode and Effects Analysis methodology (experience)
- Awareness of problem-solving methodologies (experience)
- Basic knowledge of statistical tools (Minitab or equivalent) (experience)
- Fluent in French and English (experience)
Responsibilities
- Support different Qualification and cleaning validation projects according to business needs
- Support troubleshooting operations on production sites
- Collaborates closely with MS&T team members and with other operational departments located in different areas
- Provides support for processes improvement (data collection, data trending, data analysis) with DMAIC methodology
- Contributes to Visual Management updates and improvements for Validation & Robustness department
Tags & Categories
Intern - Manufacturing Science and Technology
Bristol-Myers Squibb
Intern - Manufacturing Science and Technology
Job Description
Master's or PhD student with a background 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 applied in the Pharmaceutical Industry 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 Fluent in French and English Support different Qualification and cleaning validation projects according to business needs, Support troubleshooting operations on production sites, Collaborates closely with MS&T team members and with other operational departments located in different areas Provides support for processes improvement (data collection, data trending, data analysis) with DMAIC methodology Contributes to Visual Management updates and improvements for Validation & Robustness department Supporting People with Disabilities
About the Role/Company
- Supporting People with Disabilities
Key Responsibilities
- Support different Qualification and cleaning validation projects according to business needs
- Support troubleshooting operations on production sites
- Collaborates closely with MS&T team members and with other operational departments located in different areas
- Provides support for processes improvement (data collection, data trending, data analysis) with DMAIC methodology
- Contributes to Visual Management updates and improvements for Validation & Robustness department
Required Qualifications
- Master's or PhD student with a background 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 applied in the Pharmaceutical Industry
- Basic knowledge of Failure Mode and Effects Analysis methodology
- Awareness of problem-solving methodologies
- Basic knowledge of statistical tools (Minitab or equivalent)
- Fluent in French and English
Skills Required
- Team player and agility
- "Think out of the box" philosophy for improvement projects
Locations
- Boudry, Switzerland
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
40,000 - 60,000 CHF / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Team player and agilityintermediate
- "Think out of the box" philosophy for improvement projectsintermediate
Required Qualifications
- Master's or PhD student with a background in Pharmaceuticals (experience)
- Good understanding of GMP rules and Pharmaceutical regulations (experience)
- Good knowledge of solid oral dosage forms manufacturing and/or packaging processes (experience)
- Good understanding of chemical and physical analytical methodologies applied in the Pharmaceutical Industry (experience)
- Basic knowledge of Failure Mode and Effects Analysis methodology (experience)
- Awareness of problem-solving methodologies (experience)
- Basic knowledge of statistical tools (Minitab or equivalent) (experience)
- Fluent in French and English (experience)
Responsibilities
- Support different Qualification and cleaning validation projects according to business needs
- Support troubleshooting operations on production sites
- Collaborates closely with MS&T team members and with other operational departments located in different areas
- Provides support for processes improvement (data collection, data trending, data analysis) with DMAIC methodology
- Contributes to Visual Management updates and improvements for Validation & Robustness department
Tags & Categories