About The Position

The Manufacturing Technician I provides general support to the manufacturing department, with a focus on injectable products, and helps ensure products are manufactured to quality standards for patients. The role works in HZ3/HZ4 clean rooms and requires appropriate gowning in each area. This is a temporary assignment scheduled to last three months, with core hours Monday through Friday, 6:00 a.m. to 2:30 p.m. The technician assists with setting up and operating labeling equipment for pre-filled syringes and/or vials, including equipment in sterile support areas, and semi-automatic packaging equipment for pre-filled syringes. The role also performs in-process sampling, testing, and inspection; assists with process-room cleaning and environmental monitoring; and sets up, executes, and cleans up the needle-cleaning process. Work must follow approved specifications, SOPs, and production records, with an emphasis on getting work right the first time. The position includes required annual hazardous-waste training and may involve hazardous-waste container and tank management and inspections, generating hazardous waste during production or sampling, and transferring hazardous waste between designated areas. The technician must respond to spills in accordance with Chemical Spill Procedures and perform other duties as assigned. The role is expected to operate in accordance with Tolmar’s Core Values, including its commitments to people, agility, ethical conduct, continuous improvement, accountability, and sustainability.

Requirements

  • High school diploma or GED.
  • Acceptable results on a basic skills assessment.
  • Working knowledge of current Good Manufacturing Practices (cGMP).
  • Ability to interact professionally with peers and members of other departments in team settings.
  • Basic computer software understanding.
  • Ability to follow and understand production records and procedures.
  • Basic math and writing skills to accurately document production activities in batch records and/or log books.
  • Attention to detail in production-documentation work.
  • Ability to operate on a fast-paced manual assembly line using basic production equipment.
  • Ability to manually assemble components.
  • Ability to stand for extended periods, up to 8 hours.
  • Ability to lift up to 40 pounds.
  • Ability to perform activities above head level.

Nice To Haves

  • Experience in a manufacturing environment.

Responsibilities

  • Assist with setup and operation of labeling equipment for pre-filled syringes and/or vials, including equipment in sterile support areas.
  • Assist with setup and operation of semi-automatic packaging equipment used to package pre-filled syringes.
  • Perform in-process sampling, testing, and inspection on the packaging line.
  • Assist with cleaning and environmental monitoring of process rooms.
  • Set up, execute, and clean up the needle-cleaning process.
  • Ensure product quality adheres to approved specifications.
  • Perform work in accordance with SOPs and production records, with an expectation of doing it right the first time.
  • Participate in required annual hazardous-waste training and carry out applicable hazardous-waste activities, including management and inspection of containers and tanks, waste generation, and transfers between designated areas.
  • Respond to spills according to Chemical Spill Procedures.
  • Perform other duties as assigned.

Benefits

  • Eligible for a quarterly incentive program.
  • A benefits package is referenced; the posting notes that not all benefits may apply because of the temporary nature of the position.
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