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Quality Control Biotechnology Jobs in Chicago, IL

bioMerieux

QC Technician II - Accellix.

Lombard, IL · On-site

$25.50 - $36.90/hr

Bachelor's degree in biotechnology, biology, chemistry, or a related scientific field * Experience with assay-based workflows, sample preparation, staining, or titration activities. * Experience ...

Actalent

Lab Technician 1

Franklin Park, IL

$20 - $24.75/hr

... quality control, biotechnology, food safety, or a regulated environment. * Strong understanding of microbiological techniques and laboratory practices. * Excellent organizational, documentation, and ...

New

ProPharma Group

Senior QC Editor

Western Springs, IL · On-site

Performs detailed QC review of clinical and regulatory documents, tables, publications, annual ... Pharmaceutical and/or Biotech background strongly preferred. * Strong copyediting, data integrity ...

ProPharma Group

QA Support

Western Springs, IL · On-site

... biotech, med device, and pharmaceutical organizations of all sizes to confidently advance ... The QA for QC Representatives will focus on approval of lab associated methods. The QA for QC ...

SNAP Diagnostics

RA QA SPECIALIST

Vernon Hills, IL · On-site

Take ownership of quality control activities related to: * Service Processes * Testing and ... Experience in medical device, pharmaceutical, biotech, or healthcare environments * Familiarity ...

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Quality Control Biotechnology information

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How much do quality control biotechnology jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for quality control biotechnology in Chicago, IL is $21.60, according to ZipRecruiter salary data. Most workers in this role earn between $18.56 and $23.75 per hour, depending on experience, location, and employer.

What is a quality control biotechnology job?

Quality Control Biotechnology jobs involve ensuring that biotechnological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet required quality and safety standards. Professionals in this field design and perform tests, analyze data, and document results to verify that products comply with regulatory guidelines. They often work in laboratories, using specialized equipment to detect contaminants or inconsistencies. These roles are crucial for maintaining product integrity and protecting public health.

What are the key skills and qualifications needed to thrive as a quality control biotechnology professional?

To thrive as a Quality Control professional in Biotechnology, you need a solid background in biology or chemistry, attention to detail, and knowledge of regulatory standards, often supported by a relevant degree. Familiarity with laboratory equipment, analytical techniques (like HPLC, PCR), and quality management systems such as GMP or ISO 9001 is typically required. Strong problem-solving skills, teamwork, and clear communication help you excel in ensuring product integrity and compliance. These skills are crucial for maintaining high product standards, meeting regulatory requirements, and ensuring the safety and efficacy of biotechnological products.

What are typical challenges faced by professionals in quality control biotechnology, and how can they be addressed?

Professionals in Quality Control Biotechnology often encounter challenges such as maintaining compliance with stringent regulatory standards, managing tight deadlines for product release, and adapting to rapidly evolving technologies. To address these issues, staying updated on regulatory changes, implementing robust documentation practices, and participating in ongoing training are essential. Collaboration with cross-functional teams, such as Research & Development and Manufacturing, also helps ensure that quality standards are integrated throughout the production process.

What is the difference between Quality Control Biotechnology vs Quality Assurance Biotechnology?

AspectQuality Control BiotechnologyQuality Assurance Biotechnology
Primary FocusTesting and inspecting biotech products to ensure they meet standardsDeveloping and implementing processes to prevent defects and ensure quality
Work EnvironmentLaboratories, testing facilitiesOffice settings, compliance departments
CertificationsGMP, GLP, laboratory certificationsGMP, ISO, audit-related certifications

While both roles aim to ensure biotech product quality, Quality Control Biotechnology focuses on testing and inspection, whereas Quality Assurance Biotechnology emphasizes process development and compliance to prevent issues. Both are essential for product integrity in the biotech industry.

How to become a quality control biotechnology specialist?

To become a quality control biotechnology specialist, candidates typically need a bachelor's degree in biotechnology, biology, or a related field. Gaining experience with laboratory techniques, quality assurance protocols, and regulatory standards such as GMP or ISO is important, and certifications like ASQ's Certified Quality Auditor can enhance prospects. Strong attention to detail, analytical skills, and familiarity with laboratory equipment are also essential for success in this role.

What does quality control biotechnology do in biotech?

Quality Control Biotechnology professionals are responsible for testing and analyzing biological products to ensure they meet safety, quality, and regulatory standards. They perform assays, validate processes, and document results using laboratory instruments and techniques, often working under Good Manufacturing Practice (GMP) guidelines. Their work helps ensure the integrity and compliance of biotech products before they reach the market.

What are popular job titles related to Quality Control Biotechnology jobs in Chicago, IL?

For Quality Control Biotechnology jobs in Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Quality Control Biotechnology jobs in Chicago, IL look for?

The top searched job categories for Quality Control Biotechnology jobs in Chicago, IL are:

Quality Control Biotechnology jobs near you
Infographic showing various Quality Control Biotechnology job openings in Chicago, IL as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $44,926 per year, or $21.6 per hour.

Quality Control (QC) Analyst II

Chicago, IL

Kashiv BioSciences, LLC
Manufacturing • 201 - 500 employees
Learn more about Kashiv BioSciences, LLCexternal

$24.75 - $33.25/hr

Full-time

Re-posted 21 days ago

Job description

Description

Position Summary


The Quality Control Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial biosimilar products in cGMP-compliant laboratories and will also be expected to be engaged in continuous improvement initiatives to drive efficiency and effectiveness of Kashiv's Quality Systems. 


A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required.


Essential Duties & Responsibilities

  • Analytical testing to support product in-process, release, and stability programs.
  • Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance.
  • Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans.
  • Work with cross-functional teams to advance projects, maintain equipment, and authoring of documents and reports.
  • Train other analysts to perform laboratory procedures and assays. Participate in internal assessments and audits as and when required.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards

Requirements

Minimum Qualifications:


Education:

  • Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 5 years of experience in a pharmaceutical/biotech QC laboratory. 
  • Alternatively, Master's degree in above areas with 3 years of experience in a pharmaceutical/biotech QC laboratory or PhD in above areas with a minimum of 2 years of experience. 

Preferred Qualifications: 


Experience:

  • Previous experience in a cGMP laboratory.
  • Strong background in protein chemistry and experience troubleshooting analytical results.
  • Demonstrated success at writing, revising, and complying with SOPs, protocols/reports, and QC methods.

Special Skills:

  • Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. 
  • Previous experience supporting regulatory inspections (e.g. PAI).
  • Familiarity with preparing regulatory dossiers and data packages for interactions between Kashiv and regulatory agencies.

Work Environment & Physical Demands:

  • Some time spent in an office doing office work (reading, writing, reviewing, and editing documents).
  • Significant amount of time spent in the laboratory.
  • Must be able to work extended hours or weekend hours as requested.
  • Must be able to lift at least 25 lbs.
  • Ability to work under pressure and meet deadlines. 
  • High-paced environment structured to meet ambitious project goals
  • Some travel may be required

Supervisory Responsibility, if any: No


This position description is not a complete list of all responsibilities, duties, or skills required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.


Kashiv BioSciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Kashiv BioSciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

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