Senior Specialist, OT Systems & Automation
Working with UsChallenging.
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.
PURPOSE AND SCOPE OF POSITION:
The Sr.
Specialist, OT System & Automation- Cell Therapy Manufacturing Systems, will support the successful implementation and operation of Process Automation systems through interaction with internal team members, peer and higher-level customers as well as external service providers.
The individual is responsible for development of and adherence to system governance procedures.
Reporting into the Site IT Digital Plant organization the candidate will be primarily responsible for configuring, supporting and managing the Operational Technology and SCADA based automation systems across the site being deployed & commissioned.
The candidate should have at least 2
years of experience in pharma/biotech with specific expertise in Manufacturing Automation disciplines.
The candidate needs to have an understanding of Good Manufacturing Practices (GMPs) and process automation.
DUTIES AND
Responsibilities:
Will work on and contribute to the Libertyville Cell Therapy Facility Automation Systems (Process automation), the data collection 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 Libertyville Cell therapy facility for the following:
Configuring and supporting the Process Automation Systems infrastructure as well as the Unit operations within the Process automation system.
Integration needs with the shop floor equipment & Data Historian configuration Help set the PAS priorities for the Libertyville site 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.
Work with enterprise PAS team and SME's to develop PAS standards, philosophy, design approach and SOPs for Summit CTF.
Will drive and support the resolution of critical PAS issues.
REQUIRED COMPETENCIES:
Knowledge, Skills, and Abilities:
Demonstrated expertise in Process Automation Systems like Rockwell, Siemens, Emerson Delta V and data collection (i.
e.
OSI PI).
Working understanding of S88, S95 and batch processing operations required.
Understanding of engineering documentation such as P&IDs, process flow diagrams and standard operating procedures.
Ability to troubleshoot control systems from the field element up through operator interfaces and databases.
Experience with control system networking technologies, PC networking technology and virtualization required.
Experience working with SQL Server or other relational databases preferred but not required.
Excellent communication skills including oral, written and formal presentations.
Strong interpersonal skills and the ability to work in a team environment.
Ability to work effectively in a fast paced multi-tasking environment.
Ability to work in a diverse work environment, manage multiple priorities, and be self-directed.
Education and
Experience:
Bachelor's degree in Engineering, IT, Science field or equivalent experience.
Must have experience with SCADA systems configuration and administration.
Must have experience with data historians.
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 Quality systems and computer system validation 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 CareersWith a single vision as inspiring as Transforming patients' lives through science(TM) , 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 email protected .
Visit careers.
bms.
com/eeo-accessibility 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.
Estimated Salary: $20 to $28 per hour based on qualifications.
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.
PURPOSE AND SCOPE OF POSITION:
The Sr.
Specialist, OT System & Automation- Cell Therapy Manufacturing Systems, will support the successful implementation and operation of Process Automation systems through interaction with internal team members, peer and higher-level customers as well as external service providers.
The individual is responsible for development of and adherence to system governance procedures.
Reporting into the Site IT Digital Plant organization the candidate will be primarily responsible for configuring, supporting and managing the Operational Technology and SCADA based automation systems across the site being deployed & commissioned.
The candidate should have at least 2
years of experience in pharma/biotech with specific expertise in Manufacturing Automation disciplines.
The candidate needs to have an understanding of Good Manufacturing Practices (GMPs) and process automation.
DUTIES AND
Responsibilities:
Will work on and contribute to the Libertyville Cell Therapy Facility Automation Systems (Process automation), the data collection 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 Libertyville Cell therapy facility for the following:
Configuring and supporting the Process Automation Systems infrastructure as well as the Unit operations within the Process automation system.
Integration needs with the shop floor equipment & Data Historian configuration Help set the PAS priorities for the Libertyville site 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.
Work with enterprise PAS team and SME's to develop PAS standards, philosophy, design approach and SOPs for Summit CTF.
Will drive and support the resolution of critical PAS issues.
REQUIRED COMPETENCIES:
Knowledge, Skills, and Abilities:
Demonstrated expertise in Process Automation Systems like Rockwell, Siemens, Emerson Delta V and data collection (i.
e.
OSI PI).
Working understanding of S88, S95 and batch processing operations required.
Understanding of engineering documentation such as P&IDs, process flow diagrams and standard operating procedures.
Ability to troubleshoot control systems from the field element up through operator interfaces and databases.
Experience with control system networking technologies, PC networking technology and virtualization required.
Experience working with SQL Server or other relational databases preferred but not required.
Excellent communication skills including oral, written and formal presentations.
Strong interpersonal skills and the ability to work in a team environment.
Ability to work effectively in a fast paced multi-tasking environment.
Ability to work in a diverse work environment, manage multiple priorities, and be self-directed.
Education and
Experience:
Bachelor's degree in Engineering, IT, Science field or equivalent experience.
Must have experience with SCADA systems configuration and administration.
Must have experience with data historians.
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 Quality systems and computer system validation 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 CareersWith a single vision as inspiring as Transforming patients' lives through science(TM) , 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 email protected .
Visit careers.
bms.
com/eeo-accessibility 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.
Estimated Salary: $20 to $28 per hour based on qualifications.
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