Legend Biotech Corporation

Operations Supervisor

Legend Biotech Corporation$96K — $126K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Science, Engineering, or related field or equivalent experience required.
  • Minimum of 6 years of operations experience in a cGMP environment in the biotech/biopharma industry.
  • Strong leadership, communication, and organizational skills are essential.
  • Proficient in Microsoft Office tools (Word, Excel, PowerPoint, Outlook).
  • Solid knowledge of cGMP regulations and FDA guidance for cell-based product manufacturing.

Responsibilities

  • Supervise CAR-T process operations, ensuring compliance with cGMP requirements.
  • Lead daily operations meetings, assigning tasks to team members for production.
  • Provide hands-on support and guidance to production personnel on the floor.
  • Support and manage manufacturing investigations and revising operational procedures.
  • Collaborate closely with Operations Manager to develop production personnel.
  • Build partnerships with Manufacturing, Engineering, and Quality teams for seamless project execution.
  • Drive continuous improvement initiatives within cell therapy Technical Operations.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • 401(k) retirement plan with company match effective on day one.
  • Eight weeks of paid parental leave after three months of employment.
  • Paid time off including 15 vacation days, 5 personal days, and 5 sick days.
  • Various additional benefits including commuter benefits and legal assistance.
Full Job Description
Legend Biotech is seeking an Operations Supervisor as part of the Technical Operations team based in Raritan, NJ.

Role Overview

The CAR-T Operations Supervisor is an exempt level position working within Technical Operations team, responsible for directing the daily production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be performed within a team-based environment, on an assigned production shift schedule.

Shift Options Available:
  • Wed-Sat, 2nd Shift


Key Responsibilities
  • Lead and supervise multiple units within the CAR-T process operations (i.e. component preparation manufacturing, MFG support operations, Mock cell, and CAR-T process) according to standard operating procedures and batch records and ensure safe and compliant manufacturing operations according to cGMP requirements.
  • Lead the daily start of shift operations meetings, the daily wrap up production meetings and assign individuals their daily production task to execute and ensure compliance and successful completion of work-related tasks.
  • Work closely with operations personnel on the production floor to provide guidance and perform production tasks as needed to help the team, in a manner consistent with safety policies, quality systems, and cGMP requirements.
  • Support manufacturing investigations, create/revise operational procedures, including manufacturing work instructions, master batch records, forms, and support and manage change controls.
  • Work closely with Operations Manager to help oversee the development of production personnel, provide input on personnel performance.
  • Build strong partnerships with Manufacturing, Engineering, and Quality to ensure seamless execution of daily production tasks and work as part of a cross-functional team to address production issues as the first point of contact for operators on the production floor.
  • Support the development of manufacturing processes, participate in various department projects, and will work with others to drive continuous improvements and efficiencies within cell therapy Technical Operations.
  • Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals.
  • Distance visual acuity of at least 20/40 (Snellen) in both eyes without corrective lenses or visual acuity corrected to 20/40 (Snellen) or better with corrective lenses.
  • Color Perception both eyes 5 slides out of 8.

Requirements
  • Bachelor's degree in Science, Engineering or related field or equivalent experience required.
  • A minimum of 6 years of operations experience within a cGMP environment in the biotech/biopharma industry. Prior experience in manufacturing, quality, or engineering is required.
  • Excellent communication and organizational behaviors skills are required.
  • Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, and Outlook) is required.
  • Availability to work in a day shift (1st or 2nd shift) is required.
  • Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell-based products, and cleanroom behaviors.
  • Must exhibit strong Leadership skills and ability to effectively communicate and influence Operations associate and convey information to Management.
  • 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, while providing clear direction to team members.
  • Strong analytical, problem solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability.
  • An ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment.
  • Clear and succinct verbal and written communication skills with an attention to detail and the ability to follow procedures.
  • Experience with Operational Excellence and/or Lean Manufacturing is an asset.
  • Ability to accommodate shift work including evenings and weekends as required by the process.
  • Ability to accommodate unplanned overtime on little to no prior notice.
  • Sufficient vision and hearing capability to work in job environment with physical dexterity sufficient to use computers and document production records
  • A working leader who can participate in production runs in critical situations when needed.
  • Ability to lift a minimum of 25 lbs. and stand for a long period of time.

#Li-RN1

#Li-Onsite

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.

Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.

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.

Pay Range (Base Pay):

$96,267-$126,351 USD

Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

About Legend Biotech Corporation

Legend Biotech Corporation is a clinical-stage biopharmaceutical company focused on developing innovative cell therapies for cancer. The company's lead product candidate, LCAR-B38M/JNJ-68284528, is a chimeric antigen receptor (CAR) T-cell therapy that is being developed for the treatment of multiple myeloma, a type of blood cancer. Legend Biotech was founded in 2014 as a subsidiary of GenScript Biotech Corporation and became an independent company in 2019. The company is headquartered in Shanghai, China and has operations in the United States and Europe.
Learn more about Legend Biotech Corporation
Size
1,071 employees
Market Cap
$8.2 billion
Industry
NASDAQ

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