Assistant Scientist, Ms&t
vor 14 Stunden
**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 position is responsible for providing support to the Boudry Manufacturing, Science and Technology (MS&T) team.
You will provide technical support to several MS&T representatives in the oversight of manufacturing activities and technology transfers, process robustness monitoring and reporting activities, data management, issuing of investigation reports and support development and optimization of departmental procedures and systems within Boudry MS&T.
The role requires organizational, prioritization, interpersonal and communication skills. In this role you will also support multiple individuals within the team, prioritizing and balancing needs and requirements.
**Duties and Responsibilities**
- Provide technical support to the MS&T technical product leads in overseeing Boudry manufacturing activities ensuring compliance and security of supply.
- Assist and/or lead low to medium risk and/or complexity investigations as applicable.
- Provide support for change control management.
- Provide support for process robustness monitoring, data management and reporting activities. Perform data analysis, interpretation and authoring reports.
- Provide support for Continued Process Verification (CPV) program and assist in Annual Product Reviews.
- Provide support for process knowledge management.
- Development and update of Technology Transfer Documents (TTDs) and Process Monitoring Plans.
- Support development and optimisation of departmental procedures and systems within MS&T including development and update of MS&T documentation (Work Instructions, Standard Operating Procedures, etc.).
- Support MS&T metrics review as applicable.
- Provide technical support to the MS&T technical product leads in overseeing technology transfers and projects.
- Prepare required CMC documentation and supports the documentation review process, if applicable.
- Participates in troubleshooting of routine problems and initiatives related to continuous improvement or development of new approaches/technologies.
- Presents information to internal and sometimes external audiences.
cGMP Responsibilities/Critical Tasks:
- Documentation (technology transfer documentation, appraisals, technical memos and reports, regulatory filing, etc.)
- Deviation investigations.
- Technical support for Change Control system
**Skills/Knowledge Required**
- Degree in Engineering, Chemistry, Pharmacy or Natural Science.
- Experience in pharmaceutical industry and in GMP validation activities are considered an asset but not mandatory.
- Experience in a multinational environment recommended, including cross-functional experience
- Approachable and helpful
- Strong interpersonal skills; strong sense of understanding the needs of individuals and groups; team player and willing to work in an environment where individual initiative and accountability to the team are required
- Open-minded, flexible, solution oriented, hands-on & fast paced
- Ability to work independently, yet effectively in a team environment as well as prioritizing workload and handling multiple tasks in a timely manner
- Reliability and ability to maintain confidentially are essential.
- Excellent written & oral communication skills.
- Ability to focus, attention to detail, analyze situations quickly and objectively and determine an appropriate course of action
- Proficient in Microsoft Office and at ease with Share Point and internal social media e.g. Yammer.
- ** Fluent in English and French (written and oral)**
**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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