Senior Manager, MSAT Cell Therapy Engineering Support, Process Data Steward
Company: Disability Solutions
Location: Bothell
Posted on: May 3, 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:
careers.bms.com/working-with-us .Position Summary: The Sr. Manager
is responsible for supporting the production of personalized cell
therapy products for both global clinical trials and commercial
supply at the Bristol Myers Squibb Cell Therapy Manufacturing Plant
in Bothell, WA. This role is an individual contributor, owning and
advancing the Process Monitoring/Statistical Process Control
program at the Bothell site, interfacing with global data stewards
to drive network-wide alignment, and driving data
organization/acquisition from manufacturing control systems for
current and new products. Work will involve data analysis using
best fit tools to determine statistical relevance and practical
significance of trends.The Sr. Manager sits on the Cell Therapy
Engineering Support (CTES) leadership team driving strategic
alignment with business and quality deliverables that require
process data backed decisions. They will support other members of
CTES and MSAT when process data and/or analysis is required. Work
will heavily involve management of stakeholder relationships with
Quality Assurance, global MSAT (Technical Operations),
Manufacturing, Information Technology, and Automation.This role is
site based at the Bothell, WA BMS manufacturing facility. 50%
on-site presence is required. May require entry to the controlled
classified manufacturing space on occasion to support process
improvements and other projects. Roles and Responsibilities:
- Own and execute the BMS Bothell Process Monitoring (ProMo)
program.
- Implement Statistical Process Control (SPC) into the ProMo
program.
- Analyze and manipulate process data to elucidate potential
patterns and trends.
- Enable identification of process improvement from
identification of patterns and trends in process data.
- Support global improvement of SPC and alignment of ProMo
programs across sites.
- Facilitate routine engagement with the ProMo program for local
and global stakeholders.
- Facilitate access to additional sources of manufacturing
process data. Systems include but are not limited to MES, DeltaV,
LIMS, etc.
- Lead cross-functional teams at and above site to enable
effective collaboration.
- Support the identification of implements effective Key
Performance Indicators (KPIs) to drive engagement and
performance.
- Work with team members to identify barriers to execution,
identify solutions, and execute or escalate for
resolution/recommendation.
- With minimal supervision, lead multiple projects and contribute
to more complex projects and initiatives for the broader site. Lead
complex technical project teams and cross-functional teams.
- Enforce and master team processes, supporting the understanding
of benefits and tradeoffs of decisions. Frequently challenges the
team processes, looking for ways to improve them.
- Measurable tactical achievements and 360 feedback highly
indicative of confidence in ability to lead initiatives of limited
scope. Some measurable strategic achievements and 360 feedback
indicative of confidence in ability to lead a mid-high level
initiatives and teams.
- Strong ability to lead and influence others. Mentor others to
accelerate their career-growth and encourage them to participate.
Proactively support other team members within area capability and
help them to be successful.
- Demonstrate multiple BMS values (Integrity, Innovation,
Passion, Urgency, Inclusion, Accountability) and work to address
perceived deficiencies. Begin to demonstrate all BMS values at
higher levels with tangible examples of each
category.Education/Experience:
- Bachelor's Degree in life sciences/engineering/STEM or
equivalent; Master's Degree preferred
- 8+ years of manufacturing or analytical experience, preferably
within biopharma, cell therapy, GMP, FDA regulated, or other
regulated environments; or equivalent combination of education and
experience
- Experience analyzing complex data sets to identify relevant
trends and patterns (utilizing a variety of statistical techniques
such as univariate control charts and multi-variate
analysis/PCA/PLS)
- Experience with Process Monitoring of a manufacturing process
utilizing statistical process control applications (ex, SAS/JMP,
Statistica, etc.)
- Experience creating and owning a program/process and driving
continuous improvement over time
- Experience utilizing key performance indicators to drive
process improvement
- Possess the professionalism and technical competency required
to represent the department before our customers, regulatory
agencies, and management.
- Strong knowledge of GMP compliance, regulations and
manufacturing operations
- Experience driving projects and actions in a cross functional
environment with timely and effective communications and a sense of
urgency to achieve immediate and future goals
- Ability to work in a fast-paced environment and manage multiple
projects and objectives in parallel.
- Must be able to identify risks in a timely manner to keep
deliverables on track.
- Proven logic and decision-making abilities, critical thinking
skills.
- Lean / Six Sigma Experience is desired The starting
compensation for this job is a range from $114,000 - $144,000, plus
incentive cash and stock opportunities (based on eligibility). The
starting pay takes into account characteristics of the job, such as
required skills and where the job is performed. Final, individual
compensation is decid ed based on demonstrated experience. For more
on benefits, please visit our BMS Careers si te. Eligibility for
specific benefits listed in our careers site may vary based on the
job and location. 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. TRAVEL
REQUIREMENTS:--- Not Applicable-NAInfrequent visits to other BMS
Cell Therapy sites and the Seattle, WA facility may be
required.WORKING CONDITIONS (US Only):This job description is
intended to describe the general nature and level of work being
performed by the person assigned to this position. The primary
duties and responsibilities are intended to describe those
functions that are essential to the performance of this job.This
job description does not state or imply that the above are the only
duties and responsibilities assigned to this position. There are
other duties and responsibilities that are considered incidental or
secondary to the overall purpose of this job. Employees holding
this position will be required to perform any other job-related
duties as requested by management within reason.BMSCART VETERAN 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--- , 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/
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.
Keywords: Disability Solutions, Kirkland , Senior Manager, MSAT Cell Therapy Engineering Support, Process Data Steward, Executive , Bothell, Washington
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