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Biotech Manufacturing Associate Jobs in Aurora, IL

Astrix Inc

Packaging Associate - Biopharmaceutical

Chicago, IL · On-site

$15.50 - $19/hr

This role will be with our client who has a global footprint in both R&D and manufacturing within ... Associate's degree or higher in Biology, Chemistry, Biotechnology, Pharmacy, or related field * 6 ...

Sotera Health

Lab Analyst I

Itasca, IL · On-site

... biotechnology, or another science-related field * Associate degree or relevant laboratory coursework * Previous laboratory, manufacturing, quality, healthcare, or other regulated-industry experience

Amgen

Sr. Data Scientist - Process Modeling

Chicago, IL · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... These capabilities support drug substance development, technology transfer, manufacture, and life ...

New

Great Lakes Group

Be Seen First

Mechanical Automation Designer

Chicago, IL · On-site

$43 - $55/hr

... manufacturability, safety, and performance. Qualifications * Associate or bachelor's degree in ... Experience in the medical device , pharmaceutical, biotechnology, laboratory automation, or life ...

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All JobsBiotech Manufacturing Associate JobsBiotech Manufacturing Associate Jobs in Aurora, IL

Biotech Manufacturing Associate information

See Aurora, IL salary details

$12

$20

$33

How much do biotech manufacturing associate jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for biotech manufacturing associate in Aurora, IL is $20.81, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.27 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What job categories do people searching Biotech Manufacturing Associate jobs in Aurora, IL look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Aurora, IL are:

What cities near Aurora, IL are hiring for Biotech Manufacturing Associate jobs?

Cities near Aurora, IL with the most Biotech Manufacturing Associate job openings:

Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Aurora, IL as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 24% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $43,288 per year, or $20.8 per hour.

Manufacturing Associate I (DS) - Chicago, IL

Unicon Pharma Inc.

Chicago, IL • On-site

Contractor

Re-posted 19 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.