Intern - Manufacturing Science and Technology
vor 2 Monaten
**Working with Us**
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
This intern position is within the Pharma Manufacturing Science & Technology department, specifically in the Process and Technology department in Boudry (six-month traineeship). The focus will be on process and project development activities managed by this department.
This position will also work closely with manufacturing, QA, QC, maintenance, and logistics departments from different manufacturing sites in a GMP environment. Collaboration with external vendors may also be required.
**Skills/Knowledge Required**
- 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 Common Technical Document architecture and manufacturing process validation (Continuous Process Verification, Critical Process Parameters, Critical Quality Attributes, Quality By Design)
- 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
**Duties and Responsibilities**
- 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 Common Technical Document architecture and manufacturing process validation (Continuous Process Verification, Critical Process Parameters, Critical Quality Attributes, Quality By Design)
- 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
**Uniquely Interesting Work, Life-changing Careers**
**On-site Protocol**
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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