Manufacturing Technician I - Aseptic (1st Shift)

Tolmar

Fort Collins (CO)

On-site

USD 42,000 - 65,000

Full time

14 days+
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Job summary

Tolmar is seeking a Manufacturing Technician I - Aseptic (1st Shift) for our Fort Collins, CO site. The role focuses on aseptic production of injectable products in an ISO environment, with clean room gowning and strict adherence to cGMP and batch records.

Core hours are Monday–Friday, 6:00 am–2:30 pm, on-site. Responsibilities include operating labeling and packaging equipment, performing in-process sampling, and maintaining aseptic techniques to ensure right-first-time quality.

Qualifications

  • High school diploma, GED or equivalent required.
  • Experience in a manufacturing environment.
  • Able to stand for extended periods and lift up to 40 lbs.
  • Able to follow SOPs and batch records.
  • Basic math and writing skills for documentation.

Responsibilities

  • Operate in clean room with gowning requirements.
  • Set up and operate labeling equipment for pre-filled syringes and vials.
  • Operate semi-automatic packaging equipment for pre-filled syringes.
  • Perform in-process sampling, testing and inspection.
  • Maintain aseptic technique in ISO 5-6 environment.
  • Ensure product quality adheres to specs.

Skills

cGMP knowledge
Detail-oriented
Team collaboration
Basic math
Computer skills
Documentation

Education

High school diploma or equivalent

Tools

Labeling equipment
Sterilization equipment
Packaging equipment

Job description

Manufacturing Technician I - Aseptic (1st Shift)

Job Category: Production

Requisition Number: MANUF005847

Apply now

  • Posted : July 9, 2026
  • Full-Time
  • On-site
Locations

Showing 1 location

Core Hours: Monday - Friday, 6:00 am - 2:30 pm

  • Training hours may vary

Purpose and Scope

The Manufacturing Technician I provides general support for the manufacturing department with a focus on injectable products, while ensuring that our products are made with quality for our patients.

Key Responsibilities

  • Perform job in a clean room environment requiring clean room gowning
  • Assist in the set up and operation labeling equipment used to label pre-filled syringes and/or vials, including equipment in the sterile support areas.
  • Assist in the set up 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 in the setup/disassembly/cleaning of the syringe filling/stoppering equipment.
  • Assist in the preparation of equipment and parts for sterilization.
  • Assist in the bulking/filtration process prior to aseptic filling.
  • Maintain proper use of aseptic technique in an ISO 5-6 environment.
  • Perform facility cleaning of critical aseptic environment as required to maintain a cGMP environment and in accordance with Standard Operating Procedures.
  • Ensure that product quality adheres to approved specifications.
  • Perform job responsibilities in accordance with standard operation procedures (SOPs) and production records with an expectation of “Right the First Time.”
  • Participate in required annual hazardous waste training. Hazardous waste involvement may include, but is not limited to container and tank management and inspections, generation of hazardous waste as a part of production or sampling processes and transfer of hazardous waste between lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill Procedures.
  • Perform other duties as assigned.

Knowledge, Skills & Abilities

  • Working knowledge of current Good Manufacturing Procedures (cGMP).
  • Interact with peers and members of other departments in team settings in a professional manner.
  • Understanding of basic computer software.
  • Ability to follow and understand production records and procedures.
  • Understanding of basic math and writing skills to accurately document production activities in batch records and/or log books.
  • Attention to detail is required for documentation in production documents.
  • Capability to operate on a fast-paced manual assembly line using basic production equipment.
  • Ability to manually assemble components.
  • Ability to stand for extended periods of time (up to 8 hours).
  • Ability to lift up to 40 lbs.
  • Ability to perform activities above your head.

Requirements

  • High school diploma, GED or equivalent required.
  • Experience in a manufacturing environment.
  • Acceptable results on basic skill assessment.

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.

Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.

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