Bristol Myers Squibb Manager, MES Development ,Digital Manufacturing in Tampa, Florida
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 .
Responsible for the development, maintenance, and support of the global Enterprise Manufacturing Execution Systems (EMES) solution that is utilized globally across the digital manufacturing network to produce medicine.
The EMES engineer’s scope is the EMES core platform, components, interfaces, custom tools, and any customizations that support digital manufacturing systems and operations, including:
Material and Inventory modules
Equipment and instrument integration
Patient scheduling system integration
General automatic recipe functionality
Custom business recipe capabilities
Batch reporting and analytics
Partner with IT and Business teams to understand requirements and develop solutions
Design, build, test and deliver standard and custom EMES capabilities to the global manufacturing network
Provide support of the EMES solution to minimize disruption to manufacturing and/or impact to product
Support administration of the central EMES development and test systems, with oversight over site EMES development, test, and production systems
Contribute to knowledge management strategy through content generation and mentoring
Identity and execute on opportunities for continuous improvement
Promote compliance with data integrity and computer system validation requirements and regulations
Promote compliance by understanding change and the impact to the validated state of the application and underlying infrastructure.
Bachelor of Science in Engineering, Computer Science or related fields with 5+ years' Life Sciences industry experience and at least 5 years’ experience in Emerson Syncade MES Or 8+ years’ experience in the Life Sciences industry, with at least 8 years’ experience in Emerson Syncade MES
At least 5 years’ direct experience designing, building, deploying and supporting automation and execution systems (Syncade, DeltaV, PI Data historian, etc.) in regulated manufacturing environments
Strong domain expertise in the application of IT to manufacturing, including a broad understanding of processes and how they are supported by IT tools and systems.
Strong knowledge of regulatory landscape and demonstrated experience with software validation.
Proven track record of successful IT/automation solution delivery
Ability to work across global sites and cultures.
Optional travel up to 5% domestically and internationally
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 science™ ”, 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.
Physical 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@example.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) 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.
Company: Bristol Myers Squibb
Req Number: R1566853
Updated: 2023-06-08 02:16:42.362 UTC
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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