Oil Processing Technician I (7:00am - 3:00pm)

Trulieve•Quincy, FL
•Onsite

About The Position

The Oil Processing Technician I works in the Processing department in Quincy, Florida, weighing, measuring, filling, and packaging medical marijuana derivatives for resale at company dispensaries. The role performs quality checks and maintains accurate labeling, packaging, counts, and tracking documentation while meeting production deadlines. Work is conducted in a fast-paced, controlled manufacturing environment and must follow cGMP and Trulieve standards for cleanliness, sterility, and product quality. The technician works under the direction of the Oil Production Manager, Oil Production Supervisor, and Team Leads. The position requires daily proximity to cannabis flower and particulates, handling organic matter, and using appropriate personal protective equipment. The schedule is 40 or more hours weekly, with flexible hours depending on department needs and occasional evenings, weekends, and holidays. A comprehensive benefits package including paid time off is offered; salary is commensurate with experience.

Requirements

  • Basic computer skills.
  • Exceptionally strong math and counting skills.
  • Ability to focus, stay on task, and demonstrate meticulous attention to detail.
  • Strong interpersonal skills and ability to work productively in a group environment.
  • Dependable, with reliable transportation.
  • Able to work in a fast-paced, controlled environment with chemicals, oils, and sharp objects.
  • Able to work under minimum supervision and pressure, and manage changes in the work schedule.
  • Must be at least 21 years of age.
  • Must pass state-mandated background screening.
  • High school diploma or equivalent experience required.
  • Must remain compliant with all legal and company regulations for working in the cannabis industry.
  • Able to lift, push, pull, move, or carry at least 50 pounds to a height of at least 5 feet and a distance of at least 50 feet, with or without mechanical assistance.
  • Able to work seated or standing at workstations for extended periods and perform the described climbing, kneeling, crouching, reaching, and frequent hand and finger tasks.
  • Able to handle organic matter daily and wear appropriate personal protective equipment.
  • Must have visual acuity, with or without aids, for tasks such as reading, viewing a computer terminal, and visually inspecting small parts or details.
  • Able to communicate conversationally with coworkers and vendors.
  • Must be available to work occasional evenings, weekends, and holidays.

Nice To Haves

  • Controls and instrumentation experience.
  • One to two years of experience in manufacturing operations.
  • Experience working in a cGMP manufacturing environment.

Responsibilities

  • Weigh, measure, and fill medical marijuana derivatives into appropriate containers accurately and efficiently.
  • Perform and document quality checks on incoming materials, processes, and finished goods.
  • Apply product labels, variable-data labels, state-mandated tags, and tamper tape as needed.
  • Package products, document work, and ensure accurate case-pack counts and tracking documentation.
  • Maintain quality control measures to ensure high-quality product packaging.
  • Maintain cleanliness and sterility in the packaging area according to cGMP and Trulieve standards.
  • Follow detailed written and verbal instructions and meet production deadlines.

Benefits

  • Paid time off
  • Comprehensive benefits package
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