Assistant/Associate Engineer, CTTO Drug Product & Vector Labs
Company: Disability Solutions
Location: Seattle
Posted on: October 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: .Title:
Assistant/Associate Engineer, CTTO Drug Product & Vector
LabsLocation: 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. Key Responsibilities:
- Design and execute experiments in the process development labs
which includes aseptic processing and operation of automated
process equipment.
- Summarize experimental data and aid in analysis to draw
conclusions.
- Participate in Root Cause Analyses to determine cause of
manufacturing process investigations.
- Coordinate with the analytical group for timely delivery of
process samples and turn-around of analytical data.
- Support production related investigations, ensuring compliance
with internal standards and regulatory requirements.
- Develop and execute manufacturing process changes and
improvement activities, and/or author technical reports for process
changes and improvements.
- Support process comparability and process validation studies
including planning, execution, and documentation management.
Support necessary technical experiments and analysis to enable
decisions related to raw materials changes.
- Contributes to ownership and advancement of work processes, and
procedures.
- Flexibility with work schedule as maintenance of cell cultures
on occasional weekends, early mornings, or evenings is
requiredQualifications & Experience:
- Degree in Biological Sciences, Chemical Engineering, Life
Sciences or related discipline.
- For Process Engineer I, BS degree with minimum of 2+ years of
relevant experience, or MS degree with minimum 1+ years of relevant
experience in biologic process/analytical development or commercial
biologic manufacturing process support.
- For Process Engineer II, BS degree with minimum of 4+ years of
relevant experience, or MS degree with minimum 2+ years of relevant
experience in biologic process/analytical development or commercial
biologic manufacturing process support.
- Excellent documentation skills and attention to detail with
cGMP experience a plus.
- Ability to effectively work in cross functional teams, meet
deadlines, and prioritize responsibilities.
- Experience working in a self-driven, performance/results
oriented, fast paced matrix environment.
- Excellent problem-solving skills.
- Able to creatively manage time and elevate relevant issues to
project lead and line management.
- Strong scientific and technical writing with excellent oral
communication skills. Preferred Qualifications:
- Experience with cell therapy process development or
manufacturing
- Proficiency utilizing MS Office products and working knowledge
of statistical software (R, JMP, Minitab)
- Experience executing investigations in support of commercial
manufacturing
- Experience with commercial product support, i.e. post-marketing
commitments, on-going validation and comparability
- Combination of experience in process development, MSAT,
clinical/commercial manufacturing, and quality.
- Operational excellence training/background 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 $69,000 -
$86,000 (at the Assistant Engineer level) and $82,000 - $102,000
(as the Associate Engineer level), 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-OnsiteBMSCARTVETERANIf 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 , Assistant/Associate Engineer, CTTO Drug Product & Vector Labs, Engineering , Seattle, Washington
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