Quality Operations External Manufacturing Internship
vor 2 Wochen
**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.
**Intern Quality Operations External Manufacturing (6 Months)**
**GENERAL DESCRIPTION**
Provides Quality Assurance support to External Manufacturing Quality Operations Team. Primary responsibility is to support Quality Operations Managers/Directors with management of Contract Manufacturing Organizations (CMOs), especially in relation to standards and relevant metrics and Drug Product batch review. Will also support, case by case, the assessment and resolution of non-conformities as they occur at BMS CMOs.
**DUTIES**
- Support the Quality Brand Lead manager in the batch review process.
- Support the Quality Brand Lead manager managing non-conformities as they raise at the CMO.
- Provide Quality Assurance support for Contract Manufacturing Operations (CMOs) within a cross functional team for change control tracking (Update change control tracker; Held the change control follow-up meetings with SME; Send reminders to SME; Address BMS questions to CMOs and ensure feedback is received in a timely manner
- Collect SME feedback on the process and propose improvements to increase the process efficiency and visibility, incl. tracking and reporting tools.
- Support the implementation of process improvements
- Manage Metrics/KPIs for change control process
- Ensure quality metrics are always up to date, consistent and accessible to the Virtual Plant Team (VPT)
**QUALIFICATIONS**
- Bachelor or master’s degree in Life Science or Pharmaceutical Industry
- Fluent in English (written, spoken).
- Knowledge in good manufacturing practices and pharmaceutical regulation is an asset.
- Familiar with use of MS office suite (Excel, Word, PowerPoint).
- Familiar with statistical software (such as Minitab) is an asset.
**SOFT SKILLS REQUIREMENTS**
- Must have strong analytical, interpersonal, communication, organization and project management skills
- Result and solution oriented
- Resilient, willing to ask and speak-up to ensure correct understanding
- Must demonstrate ability to present ideas, issues and observations into a clear and useful format and balance several projects in a fast-paced team environment
- Must have the ability to collect, analyze and integrate information by leveraging appropriate PC/Systems technology including Word, Excel, Share-point and PowerPoint.
**Uniquely Interesting Work, Life-changing Careers**
**On-site Protocol**
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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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