Legend Biotech Corporation
QC Specialist, Lab Services, II/III
Legend Biotech Corporation, Raritan, New Jersey, us, 08869
About Legend Biotech
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 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. Position
QC Specialist, Lab Services II/III
– Quality team based in
Raritan, NJ . Role Overview
The QC Specialist, Lab Services is responsible for sample management and is encouraged to work independently on routine tasks while maintaining a conceptual understanding of all QC functions and business areas. The specialist may require supervision to resolve sophisticated issues and will serve as a technical specialist within the job function, thinking logically and acting 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 Microsoft Office applications (Outlook, Excel, Word, PowerPoint) and lab management software system (LIMS) Prepare documents and coordinate sample shipment (internal and external) 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 (including weekend and evening work as required by the manufacturing process) Position will be located in Raritan, NJ and may require up to 5% travel Position will occasionally require lifting up to 20 pounds Salary
Anticipated base pay range: $70,671 – $92,757 USD. Benefits
We offer a best‑in‑class benefits package that supports well‑being, financial stability, and long‑term career growth. Highlights include medical, dental, and vision insurance; a 401(k) retirement plan with company match that vests fully on day one; equity and stock options for eligible roles; eight weeks of paid parental leave after three months of employment; a paid time‑off policy featuring 15 vacation days, 5 personal days, 5 sick days, 11 U.S. national holidays, and 3 floating holidays; flexible spending and health savings accounts; life and AD&D insurance; short‑ and long‑term disability coverage; legal assistance; supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance; commuter benefits; family planning and care resources; well‑being initiatives; and peer‑to‑peer recognition programs. EEO Statement
Legend Biotech is a proud equal‑opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by applicable law. 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. Legend Biotech maintains a drug‑free workplace.
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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 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. Position
QC Specialist, Lab Services II/III
– Quality team based in
Raritan, NJ . Role Overview
The QC Specialist, Lab Services is responsible for sample management and is encouraged to work independently on routine tasks while maintaining a conceptual understanding of all QC functions and business areas. The specialist may require supervision to resolve sophisticated issues and will serve as a technical specialist within the job function, thinking logically and acting 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 Microsoft Office applications (Outlook, Excel, Word, PowerPoint) and lab management software system (LIMS) Prepare documents and coordinate sample shipment (internal and external) 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 (including weekend and evening work as required by the manufacturing process) Position will be located in Raritan, NJ and may require up to 5% travel Position will occasionally require lifting up to 20 pounds Salary
Anticipated base pay range: $70,671 – $92,757 USD. Benefits
We offer a best‑in‑class benefits package that supports well‑being, financial stability, and long‑term career growth. Highlights include medical, dental, and vision insurance; a 401(k) retirement plan with company match that vests fully on day one; equity and stock options for eligible roles; eight weeks of paid parental leave after three months of employment; a paid time‑off policy featuring 15 vacation days, 5 personal days, 5 sick days, 11 U.S. national holidays, and 3 floating holidays; flexible spending and health savings accounts; life and AD&D insurance; short‑ and long‑term disability coverage; legal assistance; supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance; commuter benefits; family planning and care resources; well‑being initiatives; and peer‑to‑peer recognition programs. EEO Statement
Legend Biotech is a proud equal‑opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by applicable law. 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. Legend Biotech maintains a drug‑free workplace.
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