Associate MES Engineer
Company: Legend Biotech
Location: Raritan
Posted on: February 6, 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 an Associate MES
Engineer as part of the Manufacturing Excellence team based in
Raritan, NJ. Role Overview The Associate MES Engineer will be part
of MSAT team reporting to the Manufacturing Execution Systems Lead
and will be responsible for interfacing with MES end users to
define change requirements while assisting with EBR development and
administration at the Raritan site to support production
processing. The associate MES Engineer will liase with other
functions including but not limited to Tech Support, Process
Improvement, Validation, Supply Chain, Operations, QA, Reg CMC, and
IT. This individual will support the MES team with electronic batch
record (EBR) updates and system improvements, support applicable
process and facility updates, and support qualification activities
associated with MES (PAS-X). Key Responsibilities This individual
will be responsible for gaining the necessary process knowledge of
the product and system knowledge of PAS-X to develop EBR designs
that fit the site’s needs. The major responsibilities will include
but are not limited to: Work with end users to define MES change
requirements Support eBR development, modeling, and deployment in
MES Participate in design testing, release planning, and demos with
partners. Support MES updates with other Supply Chain Systems (ERP,
eLIMs, etc.). Support MES validation activities according to the
Software Development Lifecycle (e.g. commissioning test Plans
(CTP), Installation/Operational Qualification (IOQ). Support
updates to standardizations and documentation (e.g. SOPs, WIs,
Technical & Design Specifications, and Qualification Protocols)
with alignment to Global Procedures. Support Site Readiness of MES
for FDA and/or Other Regulatory Audits / Inspections. Establish key
stakeholder relationships with internal and external stakeholders.
Ability to interact with all levels within the organization. This
individual is responsible for collecting the necessary information
and user requirements to ensure that the MES team properly assesses
updates and impact. Requirements A minimum of a Bachelor’s degree
in engineering or related field or equivalent experience required.
Advanced degree preferred. A minimum of 3 years of relevant
experience working in a GMP environment is required. Demonstrated
experience working cross functionally with multiple departments
translating business needs to change requirements. Cell/Gene
Therapy cGMP manufacturing and MES (PAS-X) experience preferred.
Working knowledge of MES application and user experience Work cross
functionally with stake holders to clearly define business needs
Accurately and reliably gauge task effort and plan work to meet
project timelines Work closely with the MES and MSAT organization
to ensure translation of changes from concept to implementation.
Ability to work independently and successfully, prioritize and
manage multiple tasks simultaneously, integrate cross-functional
issues and balance competing priorities effectively. Must be able
to manage shifting priorities to meet critical deadlines in a fast
paced and dynamic, growing environment. Provide technical
recommendation and limitations associated with MES functionality in
the evaluation of potential process changes for effectiveness,
value, risk. When necessary, support studies related to process
improvement and implementation of new manufacturing execution
system technologies. An ability to build strong partnerships and
effectively integrate with cross functional collaborators to drive
projects/programs forward in a matrixed environment. Strong
analytical, problem solving and critical thinking skills and the
ability to lead as a change agent to promote flexibility,
creativity, and accountability. Clear and succinct verbal and
written communication skills. Li-Onsite Li-RN1 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: $93,463 - $122,670 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, Stratford , Associate MES Engineer, Engineering , Raritan, Connecticut
