1

Biotech Manufacturing Jobs in Chicago, IL (NOW HIRING)

Manufacturing System Engineer

Lombard, IL · On-site

$104K - $129K/yr

Description Manufacturing Systems Engineer Position Summary The Manufacturing Systems Engineer is ... Experience working in GMP-regulated industries (medical devices, pharmaceuticals, biotechnology ...

Manufacturing System Engineer

Lombard, IL · On-site

$104K - $129K/yr

Manufacturing Systems Engineer Position Summary The Manufacturing Systems Engineer is responsible ... Experience working in GMP-regulated industries (medical devices, pharmaceuticals, biotechnology ...

Be Seen First

Previous experience in pharmaceutical, biotech, chemical, food, or other regulated manufacturing environments. * Familiarity with cGMP manufacturing practices. * Experience weighing, measuring ...

New

Manufacturing System Engineer

Lombard, IL · On-site

$104K - $129K/yr

Description Manufacturing Systems Engineer Position Summary The Manufacturing Systems Engineer is ... Experience working in GMP-regulated industries (medical devices, pharmaceuticals, biotechnology ...

Project Architect - Life Sciences

Chicago, IL · On-site

$85K - $114K/yr

Lead the architectural design and technical execution of life sciences manufacturing projects, including pharmaceutical and biotechnology facilities. * Translate client operational workflows ...

Project Architect - Life Sciences

Chicago, IL · On-site

$85K - $114K/yr

Lead the architectural design and technical execution of life sciences manufacturing projects, including pharmaceutical and biotechnology facilities. * Translate client operational workflows ...

next page

Showing results 1-20

Biotech Manufacturing information

See Chicago, IL salary details

$12

$21

$34

How much do biotech manufacturing jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for biotech manufacturing in Chicago, IL is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $16.88 and $24.04 per hour, depending on experience, location, and employer.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.

What are the key skills and qualifications needed to thrive in biotech manufacturing?

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are popular job titles related to Biotech Manufacturing jobs in Chicago, IL?

For Biotech Manufacturing jobs in Chicago, IL, the most frequently searched job titles are:

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

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

Infographic showing various Biotech Manufacturing job openings in Chicago, IL as of August 2026, with employment types broken down into 89% Full Time, 6% Part Time, 3% Contract, and 2% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $44,683 per year, or $21.5 per hour.

Manufacturing Associate I (DS) - Chicago, IL

Unicon Pharma Inc.

Chicago, IL • On-site

Contractor

Re-posted 13 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.