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. 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.

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.

The MSAT Manufacturing Systems Engineering and Operations Manufacturing Systems Automation and Data Analytics Engineer is accountable for leading activities and assigned resources responsible for Data Analytics solutions and insights (SQL, Azure AI, Phyton - Domino -Jupiter Notebook, Tableau, Power BI, Spotfire, and others), and for supporting the solution intake and design, delivery, operational support, continuous improvement, change management, and lifecycle for the site Automation Systems (Process Automation System, Manufacturing Execution System, and Data Historians) and associated boundary systems used in the production and monitoring of personalized cell therapy products for both global clinical trials and commercial supply. The Senior Manager will play a vital role in the leadership, organization, and integration of Site MSAT and Cell Therapy Global Manufacturing network at Bristol-Myers Squibb. The position requires strong leadership, project management skills, and stakeholder coordination.

Shift Available:

Monday - Friday, Hybrid Day Shift, 8 a.m. - 5 p.m.

Responsibilities:

Be a thought leader in data analytics, closely working with Manufacturing and Technical Operations subject matter experts to define, prioritize, and document business needs and solution requirements, study and understand the underlying data.

Provide technical direction and expertise across Site teams (Manufacturing, Quality, Supply Chain, Share Services, etc.) to support and improve capacity, quality, and cost, or to establish root cause.

Work closely with end users/process owners to establish and maintain service level expectations across all functions and site systems.

Lead the Automation and Data Intake (assessment) and backlog of proposals and requests to utilize resources efficiently and ensure alignment with Site objectives, Network policies, practices, and Senior Leadership direction.

Leads and delivers key improvements across the manufacturing network by deploying recipe updates, manufacturing data analysis reports, and technical insight.

Provide MES product impact assessments to support investigations and product release.

Develop inputs into digital solutions, such as electronic batch records and process automation technologies, to advance the digital manufacturing strategy.

Ensuring automation and data analytics solutions are configured for intended use per business requirements and applicable procedures throughout the solution lifecycle from design to implementation.

Support lifecycle management project implementation at the site level to achieve drug product harmonization across sites and refine the process.

Translate business requirements into functional and design specifications that are compliant, efficient, and effective.

Participate on project teams to help prepare project schedules, execute technical projects, and develop presentations to disseminate results to project stakeholders and senior management.

Support the change initiatives and the implementation of process improvement initiatives.

Foster strong inter-team relationships to achieve common goals.

Interface with Manufacturing groups, Quality groups, Supply Chain, IT, MSAT groups, etc. and serve as applicable Manufacturing Automation System Business Owner.

Manufacturing Automation System Business Owner for critical manufacturing systems. Accountable for leading and effective partnerships and interface with Manufacturing, Quality, Supply Chain, IT, MSAT groups, etc. to fulfill Manufacturing System Business Owner role requirements.

Oversee and support process monitoring initiatives, including but not limited to developing and collecting data, analyzing and optimizing the end-to-end process, and anticipating and permanently resolving issues that may arise during production.

Continuously integrates with the business to understand current business processes and to provide technology guidance that enables and supports Digital Plant plans and strategies.

Stay current with industry trends and standards (e.g., PDA, ISPE) and participate in best practice forums consistent with function responsibilities.

Assist with revisions of technical documentation content (e.g., investigations, changes, SOPs, and process related).

Interact with other teams, including Technical Product Team, Validation, Development, Operations, QA, and Regulatory.

Participate in routine plant operating meetings (i.e., Tiers, Townhalls, MSAT Extended Staff, etc.).

Proven ability to accurately and completely understand, follow, interpret, and apply Global Regulatory and cGMP requirements.

Support health authority and internal inspections.

Knowledge & Skills:

Ability to lead, train, and foster a cohesive team.

Advanced critical reasoning and decision-making skills.

Ability to think strategically and translate strategy into actions.

Ability to work independently and in cross-functional teams.

Advanced technical document writing.

Advanced time management skills, including prioritizing and managing expectations in a fast-paced working environment.

Must have excellent organization skills and the ability to manage multiple tasks.

Operate effectively and with moderate supervision within a team or independently, performing projects and related duties.

Intermediate knowledge of MS Office Applications.

Hands-on experience with SQL.

Hands-on experience with Python (or R) and its data science packages.

Knowledge of Machine Learning models and libraries.

Proficiency with reporting/visualization tools.

Good understanding of data analytics cloud infrastructure and various technologies comprising it.

Working knowledge of Electronic Batch Records (EBR), Review by Exception (RBE), and MES Recipe object lifecycle management preferred.

Experience with HP ALM, Electronic Document Management Systems, and Change Management Systems preferred.

Knowledge of cGMPs and multi-national biopharmaceutical regulations. Cell therapy experience is preferred.

Knowledge of the relationship between manufacturing processes, ERP, PCS, and MES preferred.

Possess strong verbal and written communication skills.

Ability to communicate honestly, transparently, and effectively with peers, department management, and cross functionally.

Hands on experience preferred with CAR T or biopharmaceutical manufacturing and Quality Control.

Ability to coach, develop, delegate, and motivate others.

Understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique preferred.

Experience with manufacturing boundary systems preferred.

Ability to travel 10% - 20% of time

Basic Requirements:

Bachelor’s degree required in Engineering, Biological/Life Sciences, Chemistry, Biochemistry or related field, or equivalent combination of education and work experience. Advanced degree preferred.

9+ years of manufacturing support, manufacturing engineering, or MS&T process engineering experience in the biotechnology/pharmaceutical industry.

2+ years of project management experience.

2+ years of SQL, Syncade MES, DeltaV, OSI Pi, ERP, LIMS, or other manufacturing boundary systems.

Understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique, packaging, shop floor quality, batch review, or disposition.

Working Conditions:

The incumbent will work in an office environment, potentially requiring ergonomic considerations.

The incumbent will be required to work in a conference room environment for moderate periods.

The incumbent will be required to work in the manufacturing labs, production areas, or warehouses requiring gowning.

The incumbent may occasionally travel between company sites for training, meetings, or corporate events.

The incumbent will be expected to work non-standard work hours, including weekends and/or holidays, to support high-priority project deadlines or emergency efforts impacting delivery.

The starting compensation for this job is a range from $130,360 to $158,000 plus incentive cash and stock opportunities (based on eligibility). 

The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. 
Final, individual compensation will be decided based on demonstrated experience. 

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Careers Site.

Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.

BMSCART, #LI-Hybrid

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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 a supportive culture, promoting global participation 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 an 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 adastaffingsupport@bms.com. 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.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

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