Sr. Associate Scientist, Quality Control
Company: Disability Solutions
Location: Indianapolis
Posted on: October 19, 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:
.RayzeBio, a Bristol Myers Squibb company, is a dynamic
biotechnology company headquartered in San Diego, CA. The company
is focused on improving survival of people with cancer by
harnessing the power of targeted radioisotopes. RayzeBio is
developing innovative drugs against targets of solid tumors. Led by
a successful and experienced entrepreneurial team, RayzeBio aims to
be the global leader in radiopharmaceuticals. RayzeBio is seeking a
Senior Associate Scientist reporting to the Sr. Manager of Quality
Control. The position will be responsible for executing and ensure
the testing and analysis of RayzeBio's radiopharamceuticals are
analyzed to cGMP standards. The applicant will be also be
responsible for mentoring junior quality control chemists, provide
technical support and liaise with other functional units, and to
maintain an appropriate laboratory safety culture. The position
will be at RayzeBio's manufacturing plant, in Indianapolis, IN.Job
Responsibilities:
- Participate in method transfer activities from CMO or internal
research facility to the production and QC teams ensuring accuracy
and reliability of data.
- Perform analyses of validated/verified methods to support novel
Radiopharmaceutical products, raw materials, and components.
- Coordinate external vendors and/or assist in the routine
calibration and maintenance of laboratory equipment.
- Participate in troubleshooting and investigation of analytical
issues, identify root causes, and implement corrective actions as
required.
- Develop and maintain appropriate documentation, particularly
data analysis
- Participate and support instrument qualification, calibration,
and maintenance activities.
- Ensure compliance with GMP regulations, safety guidelines, and
quality standards.
- Work with RSO to ensure laboratory to ensure compliance with
established radiation safety programs
- Assist in the reviewing and/or drafting of Standard Operating
Procedures and other documents
- Occasional work outside first shift is expected on an as-needed
basis.
- Up to 10% of travel may be required.Prefered Education and
Experience:
- BS in chemistry or related field with 3-7 years of experience
in pharmaceutical field OR MS in chemistry or related field with
2-5 years of experience in pharmaceutical field.
- Experience testing in a quality control chemistry lab is
required. Prefered Education and Experience:
- Experience handling radioactive materials is strongly
preferred. Skills:
- Highly motivated and organized professional with the ability to
work independently or in a team environment.
- Multi-disciplined scientist with GMP experience
- Experience with root cause techniques such as 6 M's, 5 Why's,
fishbone, or similar preferred.
- Very personable with strong communication skills
- Ability to multi-task and prioritize work based on multiple
work-flows.
- Good organizational skills are required.
- Work with multiple computer systems, including Microsoft
Office, and chromatography systems.
- Excellent professional ethics, integrity, and ability to
maintain confidential information.Physical Demands:While performing
the duties of this job, the employee is regularly required to sit,
reach with hands and arms, and talk or hear. The employee must
occasionally lift and/or move up to 40 pounds. Specific vision
abilities required by this job include close vision and distance
vision. This is a position that requires working in a laboratory
environment, protective clothing, gloves, and safety glasses are
required while working in a laboratory environment with radioactive
materials . Work Environment:The noise level in the work
environment is usually moderate.#rayzebio #LI-onsiteIf 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, Bloomington , Sr. Associate Scientist, Quality Control, Other , Indianapolis, Indiana
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