Manufacturing Technician I - Aseptic (3rd Shift)

Tolmar; Fort Collins (CO); On-site; USD 35,000 - 50,000; Full time

Job summary

A leading pharmaceutical company in Fort Collins is seeking a Manufacturing Technician I for the 3rd shift. The role involves providing support in a clean room environment for injectable products while adhering to cGMP standards. Candidates will assist in operating packaging equipment and performing quality checks. A high school diploma and experience in manufacturing are required. This full-time position offers on-site work with core hours from 10:00pm to 6:30am and emphasizes attention to detail and teamwork.

Qualifications

• Experience in a manufacturing environment is required.
• Ability to manually assemble components.
• Ability to lift up to 40 lbs.

Responsibilities

• Perform job in a clean room environment requiring clean room gowning.
• Assist in the setup and operation of semi-automatic packaging equipment.
• Maintain proper use of aseptic technique in ISO 5-6 environment.

Skills

Working knowledge of current Good Manufacturing Procedures (cGMP)

Ability to operate on a fast-paced manual assembly line

Attention to detail

Basic math and writing skills

Education

High school diploma, GED or equivalent

Job description

Manufacturing Technician I - Aseptic (3rd Shift)

Job Category: Production

Requisition Number: MANUF005736

• Posted : April 10, 2026
• Full-Time
• On-site

Locations

Showing 1 location

Core Hours: Monday - Friday, 10:00pm to 6:30am

• 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.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.