Sr. Specialist, OT Systems

4 weeks ago

Other US Location Bristol Myers Squibb Full time

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:

Duties / Responsibilities

  • Will work on and contribute to the Summit Cell Therapy Facility Automation Systems (Process automation), the data collection (OSI PI) and analytics deliverables.
  • Partnering with Mfg. Operations colleagues (Manufacturing, MS&T, Quality, Site Engineering), Enterprise teams (Global MS&T, Enterprise MES), Enterprise Business teams and local system Digital Capability Managers to deliver the requirements for the Summit Cell therapy facility for the following:
    • Delivering the requirements for the Process Automation Systems (DeltaV) infrastructure as well as the Unit operations within the Process automation system.
    • Integration needs with the Manufacturing Execution System (Syncade) & Data Historian (OSI PI)
  • Help set the PAS priorities for the Summit CTF and work the delivery of these priorities.
  • Work with the technical teams to develop the requirements, code and test the deliverables and drive execution of system testing at the site level.
  • Network and work with other cell therapy PAS members to proactively identify issues with cell therapy-based requirements and drive the resolutions.
  • Participate in DeltaV Recipe Creation
  • Responsible for maintaining and developing GMP Specifications for Process Automation Systems
  • Responsible to integration of site Building Automation System into OSI PI
  • Responsible for integration and deployment of new OT Systems (i.e Cytiva Chronicle / LOVO DXT)
  • Responsible for troubleshooting manufacturing issues related to DeltaV & OSI PI
  • Responsible for editing and developing SOPs related to Process Automation Systems
  • Assist with investigations / deviations related to site Process Automation System

Qualifications

  • Bachelor's degree in Engineering, IT, Science field or equivalent experience.
  • Must have experience with Emerson DeltaV.
  • Must have experience with OSI Pi.
  • Must be familiar with IT Architecture
  • Minimum 2+ year's relevant industry experience.
  • Prior Biologics/Cell Therapy experience is highly valued but not required.
  • Understanding of supply chain, manufacturing domains and supporting technology including manufacturing and supply chain ERP systems (e.g. Oracle, SAP).
  • Working knowledge of regulatory requirements and how they relate to existing and new business systems and practices, primarily GxP.

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 Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through scienceTM ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS 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. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to Visit to access our complete Equal Employment Opportunity statement.

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.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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