Assistant Scientist, Clinical QC- Cell Therapy

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.

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. Read more: careers.bms.com/working-with-us.

Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today. With therapies only in their infancy and BMS’s continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.

Position Summary

The primary responsibility of this position is to play a critical role in driving the digital transformation of clinical operations, with a specific focus on Smartsheet’s, LIMS, Data Management/Verification activities and the implementation of digital logbooks and forms. This position requires a candidate with 1-3 years of experience with a preferably strong GMP background who will be responsible for optimizing digital capabilities to enhance efficiency, compliance, and productivity.

Duties and Responsibilities

Smartsheet Expertise:

• Develop, manage, and optimize Smartsheet’s solutions to streamline workflows and data management.
• Collaborate with cross-functional teams to identify areas for Smartsheet’s integration and provide solutions.

LIMS Proficiency:

• Utilize CELabs LIMS to support laboratory information management, ensuring data accuracy and compliance.
• Troubleshoot and resolve any technical issues related to CELabs LIMS.
• Build Local Master Data and work collaboratively with cross functional and Global LIMS team to route PLAN and LIMS documents for UAT testing and into production.

Digital Logbooks and Forms Implementation:

• Act as a workstream lead for the implementation of digital logbooks and forms via the eLogbook system for site adoption.
• Train staff on the use of digital logbooks and forms and provide ongoing support.

GMP Compliance:

• Ensure all digital solutions and processes adhere to GXP guidelines, including data integrity and security.
• Initiate Deviations and/or CAPA, Change Controls as needed within the Infinity Quality System.

Digital Strategy Development:

• Collaborate with senior management to develop and execute a digital strategy that aligns with the company's goals and objectives.
• Stay current with digital trends and technologies to recommend improvements and innovations.

Data Analytics and Reporting:

• Analyze data collected through digital systems to identify trends, patterns, and opportunities for process improvement.
• Generate reports and dashboards to provide actionable insights to stakeholders.

Documentation and Training:

• Create and maintain documentation for digital processes, procedures, and best practices. Author and/or Review SOP’s, WP’s, PLAN’s, FORM’s etc.
• Conduct training sessions for employees on digital tools and systems.

Data Management / Verification:

• Perform data management activities related to SPARTAN.
• Perform data verification activities related to regulatory filings.

Cross-Functional Collaboration:

• Collaborate with IT, Quality Assurance, and other departments to ensure seamless integration of digital solutions.
• Act as a liaison between technical teams and end-users to address any issues or enhancements.
• Perform any other tasks or responsibilities as assigned.

Education & Experience

• Bachelor’s Degree in Life Science discipline
• 1-3 years of relevant work experience, preferably in a GMP regulated environment.
• Experience with LIMS preferred

BMSCART

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interest