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Operations Gowning Trainer

Job in Raritan, Somerset County, New Jersey, 08869, USA
Listing for: Legend Biotech USA
Full Time position
Listed on 2026-07-03
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Production QC/QA, Production Associate / Production Line
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Legend Biotech is seeking an Operations Gowning Trainer I as part of the Raritan Training team based in Raritan, NJ
.

Role Overview

This position is responsible for performing manufacturing gowning training and the execution of gowning training tasks within a CGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations.

Key Responsibilities
  • Support the Gowning Training Program responsible for clinical and commercial operation in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment.
  • Execute Instructor Led Trainings (ILT), Qualifications, and Requalification of Raritan CAR‑T Personnel.
  • Execute manufacturing gowning activities to support cell culturing, purification, aseptic processing, and cryopreservation using appropriate gowning techniques.
  • Perform gowning training and execution that follows standard operating procedures and batch records, and record production data and information in a clear, concise, format according to Good Documentation Practices (GDP).
  • Perform tasks on time in a manner consistent with quality systems, cGMP, and Learning Management System (LMS) requirements.
  • Work in a team based, cross‑functional environment to complete production tasks required by shift schedule.
  • Aid in the development of manufacturing gowning processes including appropriate documentation.
  • Drive continuous improvement of gowning techniques and processes leveraging own observation as well as input of team members.
  • Support schedule adjustments to meet production and business needs.
  • Accurately complete documentation in SOP's, logbooks, GMP documents, and training events.
  • Demonstrate training progression through assigned curriculum.
  • Accountable for maintaining a working knowledge of basic cGMP requirements to ensure adherence to compliance policies and regulations.
  • Wear the appropriate PPE when working in manufacturing and other hazardous working environments.
  • Proactively maintain a clean and safe work environment. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors.
  • Ensure materials are available for qualifications and training.
  • Support the ongoing production schedule by:
    • Report to work on‑time and according to the shift schedule.
    • Perform other duties as assigned.
    • Attend departmental and other scheduled meetings.
    • Practice good interpersonal and communication skills.
    • Demonstrate positive team‑oriented approach in the daily execution of procedures.
    • Promote and work within a team environment.
    • Learn new skills, procedures and processes as assigned by management and continue to develop professionally.
    • Support investigation efforts as required.
    • Responsible for audit preparation and participation.
Requirements
  • HS Diploma required with 4‑6 Years Biotech/Pharmaceutical experience or equivalent industry experience OR Bachelors degree required in Life Sciences or Engineering, with 0‑2 years Biotech/Pharmaceutical experience or equivalent industry experience.
  • Interpret a variety of instructions furnished in written, oral, diagram or schedule form.
  • Follow instructions.
  • Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
  • Add, subtract, multiply and divide in all units of measure, using whole numbers, common factions, and decimals.
  • Knowledge and ability to operate manufacturing, manufacturing‑support and lab equipment.
  • Knowledge of Process Excellence Tools.
  • Possesses solid knowledge of routine and non‑routine testing and sampling methods, techniques and related equipment.
  • Needs to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position.
  • Is frequently required to communicate with coworkers.
  • While performing the duties of this job, the employee is regularly required to stand, walk, climb, bend and stop, and reach with hands and arms.
  • Ability to lift 25 lbs.
  • Needs to perform gowning procedures to work in manufacturing core.

Please note:
These benefits are offered exclusively to…

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