Metrology Tech I

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life‑threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T‑cell (CAR‑T), T‑cell receptor (TCR‑T), natural killer (NK) cell‑based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting‑edge therapies for patients worldwide. Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta‑cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma. Legend Biotech is seeking a Metrology Tech as part of the Technical Operations team based in Raritan, NJ. Role Overview This position will be responsible for metrology support for cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with various Technical Operation functions in support of personalized cell therapy production through safe and compliant manufacturing operations according to cGMP requirements. This individual will support organization build and ramp‑up of clinical production and facility approval of a state of the art cell therapy facility for commercial launch and sustained production. The role will require proven technical expertise and troubleshooting ability to drive effective communication, coordination and collaboration across relevant cross functional groups to enable robust production, testing and release of product to patients. Key Responsibilities Provides technical expertise in support of an effective calibration program that supports daily clinical production and strategically prepares for commercial supply of a CAR‑T product. Plans, coordinates, and performs timely execution of daily activities related to calibration and instrumentation. Ensures proper materials, tools, standards, parts and spare parts are identified and available. Performs work review, approval and close out of work orders, including management of third‑party vendor work, in accordance with established guidelines and operating procedures. Supports the planning, coordination, and performance of timely calibration during shutdowns. Responsible for performance of IFM calibration outcomes; reviews CPI/KPI/GPI where applicable. Participates in the development of calibration data sheets, metrology job plans and associated master plans. Participates in the development, implementation and sustainment of emergency response programs and other safety programs. Assists in the creation, tracking and completion of metrology related SOPs, quality events, CAPAs, Out of Tolerance (OOT) situations and other technical documentation. Conducts basic risk mitigation options and advanced troubleshooting to identify root cause and appropriate corrective actions for equipment system problems. Helps support the optimization of calibration frequencies through a calibration interval management program including minimally invasive instrumentation tasks which support calibration interval extension. Partner with stakeholders assist in defining user requirements for new instruments. Responsible for working with groups to provide start‑up, commissioning, and qualification/validation support of instrumentation and systems including on‑the‑floor troubleshooting of equipment. Promotes a collaborative work environment focused on an EHS first mindset, a Right First Time culture of quality, permanent inspection readiness compliance mindset and passionately drives continuous improvement. Provides technical expertise in area of responsibility by effectively interfacing and collaborating with key stakeholders and functions. Actively participates in all regulatory and internal audits of the facility. Partner and manage relationships with contractors to ensure quality of work and compliance with all company policies and regulatory guidelines. Helps improve metric performance to drive team results in areas of EHS, quality, compliance, cost, delivery and people. Ability to interact with all levels within the organization. Operations, Quality, HSE, Supply Chain, Warehouse, Training, QC, EM, Operations Technical Support, Facilities and Engineering, ValidationQualification. Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals. Requirements B.Sc./M.Sc. in Biological/Biochemical Science/Bioengineering related field. Trade / Technical School Certification or Certification in Craft required. Military equivalent of Trade / Technical School certification. Minimally 4+ years of experience in cGMP cleanroom manufacturing experience under aseptic conditions. Technical knowledge in metrology, calibrations, instrumentation, automation PLCs, VFDs and electrical practices generally attained through hands‑on experience, cGMP compliance, EHS and regulatory standards (e.g. EPA, OSHA and DEA). Experience in a growth environment managing the fast pace of change, balancing day to day operational demands with the need to extend and improve the planning horizon to prepare for tomorrow. A history of being a member of high performing teams with a strong sense of mission. Communicates effectively with people at all levels, including the ability to understand their priorities, and to earn their respect and trust, along with the willingness to provide them with the best decisions in time‑sensitive situations. Capable of thriving in a fast‑paced, challenging, entrepreneurial and team‑oriented environment. Excellent teamwork and interpersonal skills with ability to influence and build strong working relationships at all levels. Proven experience working and leading in a matrix environment. Ability to lead with influence. cGMP manufacturing. Metrology, calibrations, instrumentation, automation PLCs, VFDs and electrical practices. Computerized maintenance management systems (CMMS). EHS and regulatory standards (e.g. EPA, OSHA and DEA). Able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members. Strong analytical, problem solving and critical thinking skills. Project management. Change management. Operational excellence, continuous improvement and lean manufacturing. Excellent organizational and communication skills. Pay Range (Base Pay)

$83,711 - $109,870 USD

Please note: These benefits are offered exclusively to permanent full‑time employees. Contractors are not eligible for benefits through Legend Biotech. Benefits and Paid Time Off 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 voluntary 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 voluntary 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. Work Authorization & Employment Eligibility Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E‑Verify program. If you are selected for employment, you will be required to complete the Form I‑9 process, and your employment eligibility will be verified through E‑Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates. 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 Notice Employment is at‑will and may be terminated at any time with or without cause or notice by the employee or the company. Privacy Notice For information related to our privacy notice, please review: Legend Biotech Privacy Notice. #J-18808-Ljbffr BioSpace