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Job Details


Bristol Myers Squibb

Specialist, Manufacturing Execution System (R1556629-en-us)

Manufacturing and Production

Manufacturing Engineer

Yearly

No

Summit, New Jersey, United States

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

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.

Purpose and Scope of Position:

The Specialist, Manufacturing Execution System is responsible for the coordination and execution of manufacturing support of Oracle EBS and Syncade MES, and associated boundary systems to maintain a compliant, effective, and efficient operation that meets or exceeds site goals and objectives.

Duties and Responsibilities:

  • Assist in designing, testing, and maintaining the EBR and related manufacturing data, including, but not limited to, items, specifications, lookups, list of values, recipes, routings, formulas, process instructions, and process variables.
  • Collaborate within the P&T department and with manufacturing, quality control, quality assurance, IT, global master data management, and PPIC personnel to determine business requirements for the design of master data.
  • Translate business requirements into a robust data design which is compliant, efficient, and effective.
  • Collaborate with peers to develop new SQL process variables required for electronic batch records by providing detailed business requirements.
  • Coordinate the testing of master data and MES recipes with peers and internal customers to ensure business requirements are achieved.
  • Maintain the recipe release process to meet manufacturing requirements and to maintain compliant, efficient, and reliable batch records and supporting data.
  • Develop and execute cGMP change controls and ServiceNow change requests for master data changes.
  • Design and create reports used for data analysis and data trending.
  • Provide department representation on site projects.
  • Collaborate with other stakeholders (global and site) to maintain and optimize product hierarchy while maintaining compliance and minimizing risk.
  • Perform other tasks as assigned.
  • Provide direct internal customer support to manufacturing, site planning, inventory control, quality assurance, quality control, global master data management, and IT.
  • Develop and provide technical training to Oracle EBS and Syncade MES users.
  • Maintain an understanding of the manufacturing processes, Oracle EBS, and Syncade MES.
  • Provide periodic on-call support to internal customers for emergent system issues.
  • Troubleshoot routine and complex problems to support internal customers.
  • Perform other tasks as assigned.

Required Competencies:

  • Advanced proficiency in Microsoft Excel
  • Advanced written and verbal communication skills
  • Intermediate knowledge of cGMP regulations
  • Intermediate proficiency in Microsoft Word and Outlook
  • Basic presentation development and delivery skills
  • Ability to provide on-call support in case of emergent issues
  • Ability to interpret / write technical documents
  • Ability to gown into Grade C and D classified environments
  • Ability to work as a team

Education and Experience:

  • Bachelor’s degree in a related field from an accredited college or university required.
  • 3 years relevant work experience required, preferably in a pharmaceutical manufacturing environment.
  • An equivalent combination of education, experience and training may substitute.

Working Conditions:

  • The incumbent will be required to gown to access classified manufacturing areas.

Definitions and Abbreviations:

  • P&T: Process and Technology
  • EBR: Electronic Batch Record
  • EBS: Enterprise Business Suite
  • cGMP: Current Good Manufacturing Practices

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

Why You Should Apply:

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMSCART

VETERAN

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.