Metrology Technician I/II
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 a Metrology Technician I/II 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
- Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals
- Ability to interact with all levels within the organization - Operations, Quality, HSE, Supply Chain, Warehouse, Training, QC, EM, Operations Technical Support, Facilities and Engineering, Validation.
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
- Transparent, Passionate, Fearless and Accountable
#Li-DD1
#Li-Onsite
The anticipated base pay range for the Metrology Technician I position is: $81,273 - $111,750 USD.
The anticipated base pay range for the Metrology Technician II position is: $93,463 - $128,512 USD.
Benefits:
We are committed to creating a workplace where employees can thrive - both professionally and personally. To attract and retain top talent in a highly competitive industry, we offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth. Our offerings are designed to meet the diverse needs of our team members and their families, ensuring they feel valued and supported every step of the way. Highlights include medical, dental, and vision insurance as well as a 401(k)-retirement plan with company match that vest fully on day one. Equity and stock options are available to employees in eligible roles, we offer eight weeks of paid parental leave after just three months of employment, and a paid time off policy that includes 15 vacation days, 5 personal days, 5 sick days, 11 U.S. national holidays, and 3 floating 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.
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.
Apply for this job
*
indicates a required field