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 .

Title: Process Automation Engineer, Principal Engineer

Location: Seattle, WA

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 Cell Therapy Drug Product Process Development organization at BMS is seeking a Principal Process Automation Engineer who will be responsible for DeltaV automation development in the Development Engineering & Automation group at BMS. The scope of responsibilities includes control systems design, equipment interface design and configuration, programming, simulation and testing, troubleshooting, project documentation and DeltaV system administration. The scope of automated system development will include cell processing equipment for cell expansion, cell washing, selection, non-viral gene editing devices, equipment for media and buffer formulation and filling systems. This position will work with global teams to design automated solutions that enable implementation of novel equipment to advance next generation cell therapy manufacturing. The Automation Engineer role will represent automation development in cross functional efforts working collaboratively with process development, manufacturing operations, site engineering & automation, IT and Facilities.

The job will be based in Seattle, Washington, with up to 10% travel to internal and external partner organization locations.

Key Responsibilities:

• Development of custom DeltaV applications for new and adapted equipment systems used in cell therapy manufacturing

• Adaptation of existing DeltaV applications to enable execution of new cell therapy process functional requirements

• Support end users (Process Development laboratory staff) with automation troubleshooting, education and training.

• Support of process equipment integration using DeltaV recipes to execute multiple fully automated unit operations

• Continued build out of the site DeltaV system as new DeltaV-controlled equipment is deployed throughout the labs

• With IT, deliver integrated solutions across multiple platforms including Emerson DeltaV, OSI PI, Emerson Syncade and custom equipment interfaces

• Provide automation impact assessments for process and equipment changes

• Partner with key stakeholders to define system requirements and functional specifications

• Identify and implement continuous improvement, efficiency, and system reliability projects.

• Collaborate with vendors in the design of DeltaV control strategies & compatible interfaces (for example OPC UA) for custom cell therapy process & analytical equipment

• Write and review technical documents associated with the development of automated control systems, including system architecture, requirements, specifications, testing protocols, etc.

• Participate in evaluation of 3rd party collaboration & partnership agreements for adherence to scope & development of internal equipment communication & automation standards

• Request quotes from vendors for automation equipment, software development and automation system maintenance services

• Participate in Factory Acceptance Test and Site Acceptance Test activities

• Maintenance of the site DeltaV process automation system to ensure user availability and compliance with BMS digital system security requirements

• Management and administration of development DeltaV systems, including back up & recovery, cyber security, network access, historian, patches & upgrades

• Interact with end users, IT, maintenance, and support groups while troubleshooting issues

• Maintain critical relationships with control system & unit operation vendors for lifecycle updates & maintenance

• Support the operational rollout of new technologies as they are deployed to development, clinical and commercial sites

• Contribute in global IT/OT alignment & coordination initiatives, particularly process automation, tech transfer activities, technology selection & documentation standards

Qualifications & Experience:

• BS in engineering, computer science or equivalent engineering discipline with 8+ years of process automation experience, 4+ years of DeltaV Batch experience and 5+ years of relevant biopharmaceutical industry experience

• Experience with cGMP/GMP, data integrity, computer system validation, safety principles, and working within a regulated industry.

• Experience with biopharmaceutical manufacturing, cell culture.

• Experience with defining class-based modules.

• Experience configuring and testing phase logic and sequence flow charts.

• Experience with control and equipment modules, state driven algorithms.

• Experience using DeltaV Live to configure graphics.

• Experience configuring and testing communication protocols including OPC UA, Ethernet IP, Modbus TCP and Profibus.

• Excellent written, verbal, and presentation skills.

• Ability to work with users to clearly define written requirements.

• Capable of adapting to rapidly changing priorities and deadlines.

• Highly motivated individual with the ability to work independently as well as on a cross-functional and global teams.

• Can-do attitude and ability to work in a highly matrixed and dynamic business environment including ability to interact and communicate to senior level executives.

• Deep scientific curiosity and commitment to advancing therapeutic innovation that provides better options for patients.

• Strong problem-solving and risk-based decision-making skills and a strong ability to influence or manage without direct authority.

• Highly developed interpersonal, communication and negotiation skills.

• Strong management skills and clear ability to influence and effectively align, motivate and empower teams to progress project goals in a cross-functional matrix environment.

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.

The starting compensation for this job is a range from $127,000 - $159,000, 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

Career 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.

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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 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 adastaffingsupport@bms.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.

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/

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: R1585367

Updated: 2024-09-17 04:22:41.865 UTC

Location: Seattle-WA

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.