What are the responsibilities and job description for the Sr Specialist IT, Cell Therapy Manufacturing Systems position at Bristol-Myers Squibb?
Transforming Lives through Science
We're on a mission to transform patients' lives through science. Every day, we're working towards this goal in every department. From optimizing production lines to the latest breakthroughs in cell therapy, our work has a real impact on people's lives.
You'll have the opportunity to grow and thrive through unique opportunities that are uncommon in scale and scope. You'll be part of high-achieving teams rich in diversity, where you can share your talents and perspectives.
Our Company Culture
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide range of competitive benefits, services, and programs that support our employees' goals, both at work and in their personal lives.
About the Role
The Sr. Specialist IT, Cell Therapy Manufacturing Systems plays a crucial role in supporting the seamless operation of manufacturing and business functions at our Cell Therapy Site. This position involves interaction with internal team members, peers, higher-level customers, and external service providers.
The individual is responsible for developing and adhering to system governance procedures and supporting multiple IT projects and ongoing work activities of moderate to high complexity. The individual will address IT issues for manufacturing and support staff. This role requires on-site presence at our facility in Summit, New Jersey, for at least 50% of the time.
Responsibilities
This role collaborates with business stakeholders and implementation partners to configure, build, and perform implementations, enhancements, and bug fixes using Syncade MES. The individual works with business process leads to design master data, recipes, and define best practices. They provide support for operationalizing the manufacturing and peripheral systems and ensure uninterrupted 24/7 operation of manufacturing systems for CAR T manufacturing, including on-call support on weekends on a rotation basis.
Requirements
Effective communication with both technical and non-technical team members. Strong interpersonal skills, particularly in teamwork, collaboration, and verbal and written communication. Knowledge of cGXP, GAMP, SDLC regulations, including 21 CFR part 11, and good documentation practices. Understanding of pharmaceutical, manufacturing, and equipment supporting Cell Therapy Commercial and clinical manufacturing. Strong technical and problem-solving skills, with the ability to work independently. Proven success in a high-performing, business results-driven environment.
Qualifications
2 years of experience in pharma/biotech projects, focusing on Manufacturing and IT disciplines. Knowledge of shop floor activities, Good Manufacturing Practices (GMPs), and process automation. Prior experience in Manufacturing Execution System (MES) and support, preferably Syncade MES. Bachelor's degree in Chemical, Mechanical, Biomedical, Electrical or Computer Engineering, or MIS discipline. Experience with reporting systems like Informetric InfoBatch. Experience with labeling systems like Bartender. Experience integrating MES with other enterprise applications like ERP(Oracle/SAP), LIMS, RTMS, etc.
We're on a mission to transform patients' lives through science. Every day, we're working towards this goal in every department. From optimizing production lines to the latest breakthroughs in cell therapy, our work has a real impact on people's lives.
You'll have the opportunity to grow and thrive through unique opportunities that are uncommon in scale and scope. You'll be part of high-achieving teams rich in diversity, where you can share your talents and perspectives.
Our Company Culture
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide range of competitive benefits, services, and programs that support our employees' goals, both at work and in their personal lives.
About the Role
The Sr. Specialist IT, Cell Therapy Manufacturing Systems plays a crucial role in supporting the seamless operation of manufacturing and business functions at our Cell Therapy Site. This position involves interaction with internal team members, peers, higher-level customers, and external service providers.
The individual is responsible for developing and adhering to system governance procedures and supporting multiple IT projects and ongoing work activities of moderate to high complexity. The individual will address IT issues for manufacturing and support staff. This role requires on-site presence at our facility in Summit, New Jersey, for at least 50% of the time.
Responsibilities
This role collaborates with business stakeholders and implementation partners to configure, build, and perform implementations, enhancements, and bug fixes using Syncade MES. The individual works with business process leads to design master data, recipes, and define best practices. They provide support for operationalizing the manufacturing and peripheral systems and ensure uninterrupted 24/7 operation of manufacturing systems for CAR T manufacturing, including on-call support on weekends on a rotation basis.
Requirements
Effective communication with both technical and non-technical team members. Strong interpersonal skills, particularly in teamwork, collaboration, and verbal and written communication. Knowledge of cGXP, GAMP, SDLC regulations, including 21 CFR part 11, and good documentation practices. Understanding of pharmaceutical, manufacturing, and equipment supporting Cell Therapy Commercial and clinical manufacturing. Strong technical and problem-solving skills, with the ability to work independently. Proven success in a high-performing, business results-driven environment.
Qualifications
2 years of experience in pharma/biotech projects, focusing on Manufacturing and IT disciplines. Knowledge of shop floor activities, Good Manufacturing Practices (GMPs), and process automation. Prior experience in Manufacturing Execution System (MES) and support, preferably Syncade MES. Bachelor's degree in Chemical, Mechanical, Biomedical, Electrical or Computer Engineering, or MIS discipline. Experience with reporting systems like Informetric InfoBatch. Experience with labeling systems like Bartender. Experience integrating MES with other enterprise applications like ERP(Oracle/SAP), LIMS, RTMS, etc.
