Specialist, Quality Control
Company: Bristol-Myers Squibb
Location: Bothell
Posted on: May 28, 2023
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: Purpose
and Scope of Position:The Quality Control Specialist is responsible
for supporting the release, stability, and in-process testing of
Cell Therapy clinical and commercial products with the Quality
Control department. This includes the ability in interface with
multiply groups, provide technical support and troubleshooting, and
when needed provide support for training and method transfers.This
is for a Wed. - Sat. 6:30am-4:30pm shiftEducation:
- Bachelor's degree or equivalent combination of education and
experience.Experience
- 4-6 years relevant analytical testing within a regulated QC
environment or equivalent combination of education and
experience.Knowledge, Skills, and Abilities
- Advance technical experience in microbiology techniques such as
gram stain, endotoxin, growth promotion and sterility testing.
- Demonstrated technical writing skills and scientific
problem-solving skills.
- Extensive knowledge and understanding of regulatory standards
as they apply to GMP laboratories.
- Ability to communicate effectively with peers, cross-functional
peers and management.
- Ability to work in a high paced team environment, meet
deadlines, and prioritize work from multiple projects.
- Ability to represent the interest of the group on
cross-function teams.
- Experience with LIMS and ELN computer applications.Key
Responsibilities
- Perform testing and data review of in-process, final product,
and stability samples of cell therapy product in accordance with
applicable procedures and cGMP requirements.
- Ensure timely completion of testing and tasks as assigned.
- Capable of handling complex issues, solving problems and
troubleshoot with minimal guidance.
- Author and revise technical documents such as test methods,
SOPs, specifications, and/or sample plans as appropriate.
- Support method transfers, method validation, and new instrument
implementation by representing site QC in cross-site protocols
reviews and approval.
- Own and lead Deviation, CAPA, Laboratory Investigations, and
Change Controls.
- Train and mentor others on Quality Control test methods and
processes.
- Champion and foster a positive and successful collaborative
quality culture.
- Lead the design, implementation and continuous improvement
projects for Quality Control systems and processes that are
technically sound, promote effective and efficient operations, and
comply with cGMP requirements.The starting compensation for this
job is a range from $65,000 -$82,000, 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
decided based on demonstrated experience. For more on benefits,
please visit our . Eligibility for specific benefits listed in our
careers site may vary based on the job and location.#BMSCART
#Veteran #Li-onsiteThis 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.WORKING CONDITIONS (US Only):
- While performing the duties of this job, the employee is
frequently required to stand; walk; sit; bend; stretch; use hands
and fingers, with various manipulations; reach with hands and arms;
and effectively communicate with others in the workplace, including
the ability to make and promptly respond to audible cues and
warnings.
- Work in areas that may have strong magnets.
- May work in areas with exposure to vapor phase liquid
nitrogen.
- Must have ability to work assigned shift (Day, Night, Weekends
and/or holidays).
- Will be required to wear personal protective equipment (PPE)
and other clean room garments daily. This may include, but not
limited to: safety shoes, safety glasses, aprons, face shields, lab
coats, full body gowns, hairnets, gloves, and hearing
protection.
- Require to work in and around laboratories and controlled,
enclosed, restricted areas, included clean rooms.
- Require to carry and/or lift up to 10 pounds several times a
day.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 ProtocolPhysical presence at the BMS
worksite or physical presence in the field is a necessary job
function of this role, which the Company deems critical to
collaboration, innovation, productivity, employee well-being and
engagement, and it enhances the Company culture.COVID-19
InformationTo protect the safety of our workforce, customers,
patients and communities, the policy of the Company requires all
employees and workers in the U.S. and Puerto Rico to be fully
vaccinated against COVID-19, unless they have received an exception
based on an approved request for a medical or religious reasonable
accommodation.Therefore, all BMS applicants seeking a role located
in the U.S. and Puerto Rico must confirm that they have already
received or are willing to receive the full COVID-19 vaccination by
their start date as a qualification of the role and condition of
employment.This requirement is subject to state and local law
restrictions and may not be applicable to employees working in
certain jurisdictions such as Montana. This requirement is also
subject to discussions with collective bargaining representatives
in the U.S.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 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: Bristol-Myers Squibb, Seattle , Specialist, Quality Control, Other , Bothell, Washington
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