Analyst, Quality Control - CAR-T (Nights) (Multiple Openings)
Company: Johnson & Johnson
Location: Raritan
Posted on: August 5, 2022
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Job Description:
Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's
Family of Companies, is recruiting for an Analyst, Quality Control
- CAR-T (Nights) (Multiple Openings)! At the Janssen Pharmaceutical
Companies of Johnson & Johnson, we are working to create a world
without disease. Transforming lives by finding new and better ways
to prevent, intercept, treat and cure disease inspires us. We bring
together the best minds and pursue the most promising science. We
are Janssen. We collaborate with the world for the health of
everyone in it. Learn more at www.janssen.com and follow us
@JanssenGlobal. Janssen Biotech, Inc. is part of the Janssen
Pharmaceutical Companies. Janssen Biotech, Inc., one of the Janssen
Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech
USA Inc., have entered into a global, strategic collaboration to
develop, manufacture, and commercialize a chimeric antigen receptor
(CAR) T-cell therapy. This innovative strategic partnership is
designed to combine the strengths and expertise of two companies to
advance the promise of an immunotherapy CAR-T platform and
investigational treatment.Are you interested in joining a team that
is positively impacting patients' lives by ensuring high quality in
our pharmaceutical products? Apply today for this exciting
opportunity!The QC Analyst is responsible for conducting
biochemical, microbiological, and/or general testing of final
product samples submitted to the QC laboratories. They are
responsible for ensuring testing is completed in compliance with
all applicable procedures, standards, and GMP regulations. They
typically work with a team of 5 - 15 other Analysts within the
functional laboratory of the Quality Control department. Key
Responsibilities: Perform analytical testing and maintain a safe
work environment in compliance with all applicable procedures, EHS,
and GMP regulations Perform peer review of laboratory data and
logbooks Utilize electronic systems (LIMS, iLAB) for execution and
documentation of testing Complete invalid assay and general
laboratory investigation records, CAPAs, and change controls Train
new laboratory personnel as needed Support Health Authority
inspections Provide input to functional laboratory meetings
QualificationsEducation: Minimum of a Bachelor's or equivalent
degree in Biology, Biochemistry, Microbiology, Chemistry, or
related scientific field is required;advanced degree (MSc., Ph.D.)
preferred Skills & Experience: Required: Minimum two (2) years of
relevant work experience Demonstrated experience successfully
working in an analytical role/level Knowledge and solid
understanding of current Good Manufacturing Practices (cGMP)
related to the QC laboratory Working knowledge of Quality systems
Proficiency in basic and advanced analytical methodologies within a
functional laboratory Basic knowledge of Compendial (e.g., USP, EP,
JP, etc.) requirements and standards Proficiency with Microsoft
Office Suite (Outlook, Excel, Word, and PowerPoint) Preferred:
Experience working in Biopharmaceutical or Pharmaceutical industry
in Cell and/or Gene Therapy Solid understanding and functional
knowledge in Flow Cytometry, qPCR, cell counts, and/orpotency
assays Proficient in performing technical writing (e.g., test
methods, SOP's, protocols, etc.) Experience, training, or
certification with Process Excellence tools and methodologies
Experience with Quality Control document reviews and regulatory
inspection processes Other: Requires ability and flexibility to
work 10-hour shifts between the operational hours of 4pm - 2am
(Wednesday - Saturday or Sunday - Wednesday), and provide
occasional support on the weekends or other shifts Requiresthe
ability to meet the physical demands (lift up to 20 lbs, stand or
sit for extended periods of time in a laboratory setting), to
perform visual inspections of materials (color, appearance,
particles, etc.), and to document observations during laboratory
testing Requires up to 5% domestic travel to other sites/locations
At Johnson & Johnson, we're on a mission to change the trajectory
of health for humanity. That starts by creating the world's
healthiest workforce. Through cutting-edge programs and policies,
we empower the physical, mental, emotional and financial health of
our employees and the ones they love. As such, candidates offered
employment must show proof of COVID-19 vaccination or secure an
approved accommodation prior to the commencement of employment to
support the well-being of our employees, their families and the
communities in which we live and work. Johnson & Johnson group of
Companies are equal opportunity employers, and the applicants will
receive consideration for employment without regard to race, color,
religion, sex, sexual orientation, gender identity, genetic
information, national origin, protected veteran status, disability
status, or any other characteristic protected by law. For more
information on how we support the whole health of our employees
throughout their wellness, career and life journey, please
visitwww.careers.jnj.com . Primary LocationUnited States-New
Jersey-Raritan-1000 US HIghway 202OrganizationJanssen
Pharmaceuticals, Inc. (6062)Job FunctionQualityRequisition
ID2206009622W
Keywords: Johnson & Johnson, Trenton , Analyst, Quality Control - CAR-T (Nights) (Multiple Openings), Professions , Raritan, New Jersey
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