Bristol Myers Squibb
Specialist - MSAT Cell Therapy Engineering Services, Process Support
Bristol Myers Squibb, Bothell, Washington, United States, 98021
Specialist - MSAT Cell Therapy Engineering Services, Process Support
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. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Position Summary
The primary focus of the Specialist - MSAT Cell Therapy Engineering Services, Process Support is to provide product and process support to Cell Therapy Manufacturing Operations at Bristol Myers Squibb's GMP facility in Bothell, WA. Is a process and product expert Authors product impact assessments to determine impact to product from deviating events Works with applicable SMEs to determine immediate corrections for manufacturing events Supports product impacting root cause investigations and identification of corrective actions Owns and drives GMP Quality System records to deliver MSAT initiatives Supports process improvement and lean initiatives to support productivity gains Makes data driven decisions and recommendations Supports MSAT driven cross-functional and cross-site projects Collaborates with global teams and other CTDO sites Responsibilities
Functions as a technology, product, and process subject matter expert Provides on-the-floor and on-site/remote troubleshooting and technical support Facilitates deviation prevention and deviation closure through site quality systems Analyzes and summarizes manufacturing data to support impact assessments and investigations Supports site risk assessment program and owns MSAT related risk assessment documentation Analyzes trends of clinical and commercial production data to drive actions for manufacturing process improvement Uses continuous improvement/lean tools to identify opportunities for process improvements and operational efficiencies Qualifications
Demonstrated problem-solving skills, including issue resolution, root cause investigations Demonstrated ability to effectively work in and lead cross functional teams, meet deadlines, and prioritize multiple projects Able to apply engineering principles and statistical analysis to resolve processing issues and evaluate process improvement opportunities Demonstrated scientific and technical acumen including technical writing skills BS and/or MS degree in Science or Chem/Bio Engineering 1+ years relevant experience in biologics or cell therapy manufacturing or development with BS, or 0+ years relevant experience with MS Bristol Myers Squibb is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.
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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. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Position Summary
The primary focus of the Specialist - MSAT Cell Therapy Engineering Services, Process Support is to provide product and process support to Cell Therapy Manufacturing Operations at Bristol Myers Squibb's GMP facility in Bothell, WA. Is a process and product expert Authors product impact assessments to determine impact to product from deviating events Works with applicable SMEs to determine immediate corrections for manufacturing events Supports product impacting root cause investigations and identification of corrective actions Owns and drives GMP Quality System records to deliver MSAT initiatives Supports process improvement and lean initiatives to support productivity gains Makes data driven decisions and recommendations Supports MSAT driven cross-functional and cross-site projects Collaborates with global teams and other CTDO sites Responsibilities
Functions as a technology, product, and process subject matter expert Provides on-the-floor and on-site/remote troubleshooting and technical support Facilitates deviation prevention and deviation closure through site quality systems Analyzes and summarizes manufacturing data to support impact assessments and investigations Supports site risk assessment program and owns MSAT related risk assessment documentation Analyzes trends of clinical and commercial production data to drive actions for manufacturing process improvement Uses continuous improvement/lean tools to identify opportunities for process improvements and operational efficiencies Qualifications
Demonstrated problem-solving skills, including issue resolution, root cause investigations Demonstrated ability to effectively work in and lead cross functional teams, meet deadlines, and prioritize multiple projects Able to apply engineering principles and statistical analysis to resolve processing issues and evaluate process improvement opportunities Demonstrated scientific and technical acumen including technical writing skills BS and/or MS degree in Science or Chem/Bio Engineering 1+ years relevant experience in biologics or cell therapy manufacturing or development with BS, or 0+ years relevant experience with MS Bristol Myers Squibb is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.
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