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Quality Control Production Associate Jobs in Elmhurst, IL

Ametek

Production Associate

Mount Prospect, IL

$15 - $19/hr

This position plays a critical role in ensuring product quality and operational efficiency while ... Production associates may be exposed to varying noise levels and moving equipment typical of a ...

Virtucom, Inc.

Technical Production Associate

Chicago, IL · On-site

$16 - $19.23/hr

Technical Production Associate - Naperville Facility We are seeking detail-oriented and motivated ... Follow established workflows, processes, and quality control standards. * Collaborate with team ...

Virtucom, Inc.

Technical Production Associate

Chicago, IL · On-site

$16 - $19.23/hr

Technical Production Associate - Naperville Facility We are seeking detail-oriented and motivated ... Follow established workflows, processes, and quality control standards. * Collaborate with team ...

Adecco

Quality Control Technician

Aurora, IL

$24/hr

Review, verify and test products across the three stages of production (incoming, in-process, and ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Virtucom Inc

Technical Production Associate

Chicago, IL · On-site

$16 - $19.23/hr

Technical Production Associate - Naperville Facility We are seeking detail-oriented and motivated ... Follow established workflows, processes, and quality control standards. * Collaborate with team ...

Integrity Trade Services

Quality Control

Chicago, IL

$20.50/hr

Integrity Trade Services is hiring a Quality Assurance Technicianfor our Food Manufacturing client ... Inspect product for proper color, texture, size, thickness, hardness, moisture, weight, etc.

ATMI PRECAST

QC Engineer

Aurora, IL · On-site

As a Quality Control Engineer, you will play a key role in ensuring that our products meet both company and industry standards. This position gives you exposure to every stage of production, from pre ...

ATMI PRECAST

QC Engineer

Aurora, IL · On-site

As a Quality Control Engineer, you will play a key role in ensuring that our products meet both company and industry standards. This position gives you exposure to every stage of production, from pre ...

ATMI Precast

QC Engineer

Aurora, IL · On-site

As a Quality Control Engineer, you will play a key role in ensuring that our products meet both company and industry standards. This position gives you exposure to every stage of production, from pre ...

Total Talent

Production Associate

Elk Grove Village, IL · On-site

$18/hr

Production Associate Location: Elk Grove Village, IL Pay Rate: $18.00/hour Shift: 1st Shift We are ... Perform quality checks on finished parts * Package and label completed products for shipment

Ionbond USA

Quality Control Inspector

West Chicago, IL · On-site

$18 - $20/hr

... audits, product audits, 5S, HSE, QMS self-assessment and customer supplied audit forms · ... Associate Degree preferred. 2+ years' experience in a manufacturing environment completing QC ...

METRAFLEX COMPANY INC

QC Analyst

Mccook, IL · On-site

$23.50 - $31.50/hr

Metraflex is a manufacturer that has been supplying piping-specialty products to the commercial HVA ... The Sales QC Analyst is responsible for conducting audits and inspections to ensure products meet ...

LabPersonnel

Be Seen First

Quality Control Technician

Elgin, IL · On-site

$50K/yr

Determine proper adjustments needed to production batches to be approved. * Write Technical Service Reports. Education & Experience background. * Science degree (Chemistry, Biology) 1(+) year of QC ...

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All JobsQuality Control Production Associate JobsQuality Control Production Associate Jobs in Elmhurst, IL

Quality Control Production Associate information

See Elmhurst, IL salary details

$11

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$38

How much do quality control production associate jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for quality control production associate in Elmhurst, IL is $25.36, according to ZipRecruiter salary data. Most workers in this role earn between $18.41 and $30.87 per hour, depending on experience, location, and employer.

What does a quality control production associate do?

A Quality Control Production Associate is responsible for inspecting products during and after the manufacturing process to ensure they meet specific standards and quality guidelines. They perform tests, record data, and identify any defects or inconsistencies in materials or finished goods. Additionally, they may work with production teams to recommend improvements and help maintain compliance with safety and regulatory requirements. Their role is essential for ensuring that only products meeting quality standards reach customers.

What are the key skills and qualifications needed to thrive as a quality control production associate?

To thrive as a Quality Control Production Associate, you need a solid understanding of quality assurance processes, attention to detail, and usually a background in manufacturing or laboratory environments. Familiarity with statistical process control (SPC) tools, laboratory testing equipment, and quality management systems like ISO standards is often required. Strong problem-solving abilities, teamwork, and effective communication skills set top performers apart in this role. These competencies ensure that products consistently meet regulatory and company standards, which is essential for maintaining safety, compliance, and customer satisfaction.

What are some typical challenges faced by quality control production associates and how can they be effectively managed?

Quality Control Production Associates often encounter challenges such as meeting tight production deadlines while maintaining high standards of accuracy and compliance. Handling repetitive tasks without losing attention to detail and navigating communication between production and quality teams are also common. To manage these challenges, associates can focus on developing strong organizational skills, staying up to date with standard operating procedures, and actively participating in cross-team meetings to clarify expectations and streamline processes.

What is the difference between Quality Control Production Associate vs Quality Assurance Technician?

AspectQuality Control Production AssociateQuality Assurance Technician
CertificationsOften requires basic quality control or manufacturing certificationsMay require certifications like ASQ CQE or ISO auditor
Work EnvironmentWorks directly on production lines, inspecting products during manufacturingWorks in labs or office settings, reviewing processes and documentation
Industry UsageCommonly employed in manufacturing, food production, and pharmaceuticalsUsed across manufacturing, food, and healthcare industries for process verification

The main difference is that a Quality Control Production Associate focuses on inspecting and testing products during manufacturing, while a Quality Assurance Technician emphasizes reviewing processes and ensuring compliance to prevent defects. Both roles require quality-related certifications and are integral to maintaining product standards in manufacturing environments.

What is the role of a quality control production associate?

A quality control production associate is responsible for inspecting products during manufacturing to ensure they meet quality standards and specifications. They perform tests, document findings, and identify defects, often using tools like calipers or microscopes, to maintain product consistency and safety.

What cities near Elmhurst, IL are hiring for Quality Control Production Associate jobs?

Cities near Elmhurst, IL with the most Quality Control Production Associate job openings:

Quality Control Production Associate jobs near you

Quality Control (QC) Analyst II

Chicago, IL • On-site

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

$24.75 - $33.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 6 days ago

Job description

Job Type
Full-time
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.

Compensation:
  • Quality Control (QC) Analyst II - Base Salary Range and Yearly Bonus (0-2 years or more of manufacturing biologics/biosimilars Quality Control experience) - $65,000 to $70,000 (dependent on years of experience and fit for the position) with up to an 8% yearly (discretionary) cash bonus

Benefits/Perks:
  • Medical Insurance - Aetna
    • Prescription Drug Converge Rx
    • Virtual Visits - Aetna/Teladoc
    • Health Savings Accounts (HSA)
    • Flexible Spending Accounts (FSA)
  • Dental Insurance - Aetna
  • Vision Insurance - VSP
  • Life and AD&D Insurance
  • Disability Benefits
  • Supplemental Benefits
    • Legal Services
    • ID Theft Protection
    • Travel Assistance
  • Value Added Benefits & Services
    • Health Advocate
    • Life Assistance Program (LAP)
    • Student Loan Assistance Program
  • 401K
  • Monthly Cell Phone Allowance
  • Free Parking (Company Paid)
  • Conveniently located next to the Metra, Green and Red Line
  • One block east of the Chicago White Sox Stadium
  • Less than 10 minutes away from Downtown Chicago

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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