BioSpace
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life‑threatening diseases. Headquartered in Somerset, New Jersey, we develop 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 worldwide, we apply these innovative technologies to pursue the discovery of safe, efficacious, and cutting‑edge therapeutics for patients worldwide.
Legend Biotech has entered a global collaboration agreement with Janssen, a Johnson & Johnson company, to jointly develop and commercialize ciltacabtagene autolecuel (cilta‑cel), an immunotherapy in the treatment of multiple myeloma.
BMS/EMS Technician – Facilities & Engineering Location: Raritan, NJ
Role Overview This position provides engineering support for building automation and controls systems in the cGMP clinical and commercial cell therapy manufacturing plant. The role handles day‑to‑day activities including life cycle management, issue remediation, deviations, corrections, and improvement of automation and controls systems for facility, equipment, and processes in support of personalized cell therapy production. It requires systems engineering experience, ownership, leadership, independent work, effective communication, coordination, and collaboration across cross‑functional teams to establish a strong, compliant program that enables robust production, testing, and release of product to patients.
Key Responsibilities
Works with plant functions to implement and maintain tools, standards, policies and procedures in compliance.
Handles day‑to‑day activities for BAS, EMS, and other automation and controls system software, hardware and associated interfaces including data management, issues, deviations, corrections, remediation and improvement.
Conducts local system data performance monitoring and analysis for BAS and EMS.
Executes against SOPs, including data backup, disaster recovery, user administration, etc.
Implements and maintains network configuration for BAS, EMS, and facility automation equipment.
Provides training to end users.
Provides user‑defined reports and facilitates ad‑hoc queries.
Provides status reports and coordinates with other departments or outside contractors/vendors to complete tasks.
Requirements
A minimum of 2 years as an automation and controls field service technician with experience troubleshooting complex systems.
Deep knowledge of Honeywell and Siemens BAS software, hardware, protocols and IT infrastructure (HC900s, CPO, PXCMs, EBI, Desigo, BACnet, MODBUS, APOGEE P2).
Experience in an aseptic manufacturing facility, preferably cell therapy or testing facility, quality assurance, or manufacturing compliance.
GMP compliance knowledge including 21 CFR Part 11, EU Annex 11 and ICH/21 CFR Parts 210, 211, 1271 (knowledge of 600, 601, 610 preferred).
Thorough knowledge and understanding of GMP data integrity standards.
Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell‑based products as well as Good Tissue Practices.
Strong interpersonal and written/oral communication skills.
Ability to process complex information and make critical decisions with limited information.
Proficiency in process excellence tools and methodologies.
Ability to independently manage a portfolio of ongoing projects.
Attention to detail and adherence to procedures.
Highly organized, team‑oriented, positive attitude with some supervision.
Experience authoring and executing documentation including batch records, SOPs, work instructions, protocols.
Experience with BAS, EMS, TrackWise, CMMS and Maximo.
Familiarity with IT application design and deployment.
Proficiency with Microsoft Office (Outlook, Excel, Word, PowerPoint).
Benefits Legend Biotech offers a best‑in‑class benefits package for permanent employees, including medical, dental, and vision insurance, a 401(k) retirement plan with company match vesting fully on day one, equity and stock options in eligible roles, eight weeks of paid parental leave after three months, paid time off (vacation days, personal days, sick time, 11 company holidays, 3 floating holidays), flexible spending and health savings accounts, life and AD&D insurance, short‑ and long‑term disability coverage, legal assistance, supplemental plans (pet, critical illness, accident, hospital indemnity), commuter benefits, family planning and care resources, well‑being initiatives, and peer‑to‑peer recognition programs. Benefits are offered exclusively to permanent employees; contract employees are not eligible.
EEO Statement Legend Biotech provides 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, 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. Legend may adjust base salary or other discretionary compensation at any time. Legend maintains a drug‑free workplace.
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Legend Biotech has entered a global collaboration agreement with Janssen, a Johnson & Johnson company, to jointly develop and commercialize ciltacabtagene autolecuel (cilta‑cel), an immunotherapy in the treatment of multiple myeloma.
BMS/EMS Technician – Facilities & Engineering Location: Raritan, NJ
Role Overview This position provides engineering support for building automation and controls systems in the cGMP clinical and commercial cell therapy manufacturing plant. The role handles day‑to‑day activities including life cycle management, issue remediation, deviations, corrections, and improvement of automation and controls systems for facility, equipment, and processes in support of personalized cell therapy production. It requires systems engineering experience, ownership, leadership, independent work, effective communication, coordination, and collaboration across cross‑functional teams to establish a strong, compliant program that enables robust production, testing, and release of product to patients.
Key Responsibilities
Works with plant functions to implement and maintain tools, standards, policies and procedures in compliance.
Handles day‑to‑day activities for BAS, EMS, and other automation and controls system software, hardware and associated interfaces including data management, issues, deviations, corrections, remediation and improvement.
Conducts local system data performance monitoring and analysis for BAS and EMS.
Executes against SOPs, including data backup, disaster recovery, user administration, etc.
Implements and maintains network configuration for BAS, EMS, and facility automation equipment.
Provides training to end users.
Provides user‑defined reports and facilitates ad‑hoc queries.
Provides status reports and coordinates with other departments or outside contractors/vendors to complete tasks.
Requirements
A minimum of 2 years as an automation and controls field service technician with experience troubleshooting complex systems.
Deep knowledge of Honeywell and Siemens BAS software, hardware, protocols and IT infrastructure (HC900s, CPO, PXCMs, EBI, Desigo, BACnet, MODBUS, APOGEE P2).
Experience in an aseptic manufacturing facility, preferably cell therapy or testing facility, quality assurance, or manufacturing compliance.
GMP compliance knowledge including 21 CFR Part 11, EU Annex 11 and ICH/21 CFR Parts 210, 211, 1271 (knowledge of 600, 601, 610 preferred).
Thorough knowledge and understanding of GMP data integrity standards.
Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell‑based products as well as Good Tissue Practices.
Strong interpersonal and written/oral communication skills.
Ability to process complex information and make critical decisions with limited information.
Proficiency in process excellence tools and methodologies.
Ability to independently manage a portfolio of ongoing projects.
Attention to detail and adherence to procedures.
Highly organized, team‑oriented, positive attitude with some supervision.
Experience authoring and executing documentation including batch records, SOPs, work instructions, protocols.
Experience with BAS, EMS, TrackWise, CMMS and Maximo.
Familiarity with IT application design and deployment.
Proficiency with Microsoft Office (Outlook, Excel, Word, PowerPoint).
Benefits Legend Biotech offers a best‑in‑class benefits package for permanent employees, including medical, dental, and vision insurance, a 401(k) retirement plan with company match vesting fully on day one, equity and stock options in eligible roles, eight weeks of paid parental leave after three months, paid time off (vacation days, personal days, sick time, 11 company holidays, 3 floating holidays), flexible spending and health savings accounts, life and AD&D insurance, short‑ and long‑term disability coverage, legal assistance, supplemental plans (pet, critical illness, accident, hospital indemnity), commuter benefits, family planning and care resources, well‑being initiatives, and peer‑to‑peer recognition programs. Benefits are offered exclusively to permanent employees; contract employees are not eligible.
EEO Statement Legend Biotech provides 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, 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. Legend may adjust base salary or other discretionary compensation at any time. Legend maintains a drug‑free workplace.
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