Process Automation Engineer, Principal Engineer
Company: Disability Solutions
Location: Seattle
Posted on: October 2, 2024
Job Description:
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: .Title:
Process Automation Engineer, Principal EngineerLocation: Seattle,
WAAt 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
standardsQualifications & 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. #LI-HybridBMSCARTVETERANIf
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--- , 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.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: Any data processed in connection with role
applications will be treated in accordance with applicable data
privacy policies and regulations.
Keywords: Disability Solutions, Seattle , Process Automation Engineer, Principal Engineer, Engineering , Seattle, Washington
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