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Associate Manufacturing Operator Jobs in Illinois

CJK Group

Manufacturing Associate - Press

Pontiac, IL · On-site

A successful and growing industry-leading company Manufacturing Associate - Press Current Openings ... Cleans work area, makes minor repairs, and otherwise assists the machine operators. * May perform ...

Aerotek

Production Associate

Waukegan, IL · On-site

$21/hr

Production Associate Shift: 7:00am-3:30pm Pay: $21/hr Join our team as a Manufacturing Operator, where you will be trained to work in four diverse areas: Assembly, Lapping, Conveyance, and Shipping ...

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Showing results 21-40

All JobsAssociate Manufacturing Operator JobsAssociate Manufacturing Operator Jobs in Illinois

Associate Manufacturing Operator information

What is the difference between Associate Manufacturing Operator vs Production Technician?

AspectAssociate Manufacturing OperatorProduction Technician
CredentialsHigh school diploma or equivalent; on-the-job trainingHigh school diploma or equivalent; technical certifications may be preferred
Work EnvironmentManufacturing floors, assembly lines, cleanroomsManufacturing facilities, laboratories, quality control areas
Job ResponsibilitiesOperate machinery, follow production processes, document activitiesMaintain equipment, troubleshoot issues, assist in process improvements

The Associate Manufacturing Operator and Production Technician roles share similar environments and entry requirements, focusing on manufacturing processes. However, Production Technicians often have more technical responsibilities, including equipment maintenance and troubleshooting, making them slightly more specialized within the manufacturing team.

What do you do as an associate manufacturing operator?

An associate manufacturing operator is responsible for operating and monitoring manufacturing equipment, assembling products, and ensuring quality standards are met. They often follow safety protocols, document production data, and may use tools like control panels or measurement instruments in a factory environment.

What cities in Illinois are hiring for Associate Manufacturing Operator jobs?

Cities in Illinois with the most Associate Manufacturing Operator job openings:

Infographic showing various Associate Manufacturing Operator job openings in Illinois as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Manufacturing Associate I (DS) - Chicago, IL

Chicago, IL • On-site

Unicon Pharma Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Unicon Pharma Inc.external

Contractor

Re-posted 2 days ago

Job description

Title: Manufacturing Associate I (DS)

Location: Chicago, IL, 60616

Position Summary:

The Manufacturing Associate I (DS), will be responsible for the manufacturing of Biotechnology products for clinical and commercial human use.

Employee applies aseptic techniques while working in controlled and classified environments, which require cleanroom gowning and some aseptic gowning.

Must comply with Client policies, procedures (SOP), FDA current Good Manufacturing Practices (cGMP), and any other government requirement.

Essential Duties & Responsibilities

Follow work instructions, production specifications, and standard operating procedures (SOPs) to perform key responsibilities and maintain quality data while meeting production goals and timelines and minimizing downtime/delays.

Work instructions include but are not limited to:

  • Weighing and dispensing of materials
  • Media and buffer preparation
  • Operation of filtration systems (such as dead end filtration, depth filtration, tangential flow filtration)
  • Inoculation, fermentation, harvest, and homogenization of cytokine cells
  • Setup and operation of chromatography columns
  • Aseptic final filtration of intermediates and drug substances
  • Monitor product for quality output using PLC controls, HMI interfacing, integrity testing, and in process testing (pH, Conductivity, and Spectroscopy).
  • Properly handle and discard hazardous materials (i.e, buffers, chemicals, etc.) in accordance with EHS guidelines. Remove used and soiled materials from manufacturing areas.
  • Follow daily and weekly cleaning routines for cleanrooms and equipment to maintain the required conditions for cleanroom manufacturing.
  • Verify raw materials and commodities; accurately enter raw material and commodities data in MES on daily basis
  • Completes Batch Records and other cGMP documentation accurately and in a timely manner.
  • Reports nonconformances or events that arise during the shift to the Supervisor
  • Complies with all safety, cGMP and Company policies, practices and procedures.
  • Performs other functions as required or assigned

Education:

  • Associate degree or higher in Biology, Chemistry, Biotechnology or related preferred
  • Or an equivalent of 0 – 2 years of industry experience required
  • Aseptic techniques and cleanroom manufacturing experience is preferred.

Language:

  • Basic verbal and written communication skills in English with the ability to understand technical information, procedures, batch records, and other documents in English.
  • Excellent interpersonal skills, effective communication with peers and supervision.

Reasoning Skills:

  • The candidate should have the ability to operate complex systems and equipment in accordance with current GMPs, SOPs, and safety guidelines under minimum supervision.
  • Basic skills for identifying problems and troubleshooting of the equipment and manufacturing processes
  • Ability to work independently, within prescribed guidelines, or as a team member and the demonstrated ability to follow detailed directions.

Computer and/or Technical Skills:

  • Skills for working with Computer systems, such as: Delta, PCR, POMS, LIMS, SAP, etc.
  • Operation and understanding of word processing, spreadsheets, and data management
  • Knowledge of GMP and safety requirements.
  • Knowledge of biotechnology operations such as, Aseptic Filtration Systems, Aseptic Sampling, Filter Integrity Testing, Fermentation Process, Inoculation Process, Chromatography Columns, Mixing systems, Weigh Scales, etc.

Work Environment & Physical Demands:

  • General work environment and physical demands as required to successfully perform the essential functions of this job.
  • Ability to work flexible hours as needed.
  • Ability to work under pressure and meet deadlines.