QC Specialist, Lab Services, II/III
Company: Legend Biotech
Location: Raritan
Posted on: January 23, 2026
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Job Description:
Legend Biotech is a global biotechnology company dedicated to
treating, and one day curing, life-threatening diseases.
Headquartered in Somerset, New Jersey, we are developing advanced
cell therapies across a diverse array of technology platforms,
including autologous and allogenic chimeric antigen receptor
T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based
immunotherapy. From our three R&D sites around the world, we
apply these innovative technologies to pursue the discovery of
safe, efficacious and cutting-edge therapeutics for patients
worldwide. Legend Biotech entered into a global collaboration
agreement with Janssen, one of the pharmaceutical companies of
Johnson & Johnson, to jointly develop and commercialize
ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is
designed to combine the strengths and expertise of both companies
to advance the promise of an immunotherapy in the treatment of
multiple myeloma. Legend Biotech is seeking QC Specialist, Lab
Services, II/III as part of the Quality team based in Raritan, NJ.
Role Overview The QC Specialist, Lab Services is responsible for
sample management. The QC Specialist is encouraged to work
independently on routine tasks and have conceptual understanding of
all Quality Control functions and business areas. May need
supervision/support to resolve some sophisticated issues. He/ She
will serve as technical specialist within job function. Thinks
logically and acts decisively. Key Responsibilities Prepares and
reviews documentation independently Responsible for QC sample and
retain management Knowledge and understanding of current Good
Manufacturing Practices (cGMP) related to the QC laboratory and
ability to identify gaps in processes or systems Proficient with
using Microsoft Office applications (Outlook, Excel, Word, and
PowerPoint) and lab management software system (LIMS) Prepare
documents and coordinate Sample shipment (internal and external
shipments) Review logbooks and/ or LIMs to align physical
quantities of samples in freezers/refrigerators Periodic inspection
and consolidation of retains Document and perform sample management
related non-conformance investigations Document and handle
corrective and preventative action records Supports internal and
regulatory audits Requirements A minimum of a Bachelor’s degree or
higher A minimum of two (2) years related experience in medical
device, biopharmaceutical, or pharmaceutical industry A degree in
Biology, Biochemistry, Microbiology, Chemistry or related field
Solid understanding of regulatory requirements, policies and
guidelines Experience with Quality Control document reviews and
regulatory inspection processes Working knowledge of Quality
systems Experience in management of retain samples using electronic
systems (eLIMS) Candidates must be able to accommodate shift
schedule. Shifts include weekend and evening work as required by
the manufacturing process This position will be located in Raritan,
NJ and may require up to 5% of travel This position will
occasionally require to lift up to 20 pounds Li-BG1 Li-Onsite The
base pay range below is what Legend Biotech USA Inc. reasonably
expects to offer at the time of posting. Actual compensation may
vary based on experience, skills, qualifications, and geographic
location. The company reserves the right to modify this range as
needed and in accordance with applicable laws. Performance-based
bonus and/or equity is available to employees in eligible roles.
The anticipated base pay range is: $70,671 - $92,757 USD Benefits
Benefits include medical, dental, and vision insurance as well as a
401(k) retirement plan with a company match that vests fully on day
one. We offer eight (8) weeks of paid parental leave after just
three (3) months of employment, and a paid time off policy that
includes vacation time, personal time, sick time, floating
holidays, and eleven (11) company holidays. Additional benefits
include flexible spending and health savings accounts, life and
AD&D insurance, short- and long-term disability coverage, legal
assistance, and supplemental plans such as pet, critical illness,
accident, and hospital indemnity insurance. We also provide
commuter benefits, family planning and care resources, well-being
initiatives, and peer-to-peer recognition programs; demonstrating
our ongoing commitment to building a culture where our people feel
empowered, supported, and inspired to do their best work. Please
note: These benefits are offered exclusively to permanent full-time
employees. Contract employees are not eligible for benefits through
Legend Biotech. EEO Statement It is the policy of Legend Biotech to
provide equal employment opportunities without regard to actual or
perceived race, color, creed, religion, national origin, ancestry,
citizenship status, age, sex or gender (including pregnancy,
childbirth, related medical conditions and lactation), gender
identity or gender expression (including transgender status),
sexual orientation, marital status, military service and veteran
status, disability, genetic information, or any other protected
characteristic under applicable federal, state or local laws or
ordinances. Employment is at-will and may be terminated at any time
with or without cause or notice by the employee or the company.
Legend may adjust base salary or other discretionary compensation
at any time based on individual, team, performance, or market
conditions. For information related to our privacy policy, please
review: Legend Biotech Privacy Policy.
Keywords: Legend Biotech, Westport , QC Specialist, Lab Services, II/III, Science, Research & Development , Raritan, Connecticut