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Quality Control Stability Jobs in Chicago, IL (NOW HIRING)

Supergut

Quality Control Manager

Chicago, IL · On-site +1

$110K - $120K/yr

SOPs and quality manuals * Maintain document control processes, revision tracking, and controlled ... Develop and maintain product-specific stability protocols * Establish and manage a long-term ...

Supergut

Quality Control Manager

Chicago, IL · Remote

$110K - $120K/yr

SOPs and quality manuals * Maintain document control processes, revision tracking, and controlled ... Develop and maintain product-specific stability protocols * Establish and manage a long-term ...

Stryker

Associate Quality Manager, Stability

Cary, IL · On-site

$112K - $188K/yr

Analyze stability data and trends to proactively identify risks, mitigate issues, and drive ... Minimum of 6+ years' experience - supporting Pharmaceutical Quality Control and Quality Assurance ...

Stryker

Associate Quality Manager, Stability

Cary, IL · On-site

$112K - $188K/yr

Analyze stability data and trends to proactively identify risks, mitigate issues, and drive ... Minimum of 6+ years' experience - supporting Pharmaceutical Quality Control and Quality Assurance ...

Stryker

Associate Quality Manager, Stability

Cary, IL · On-site

$188K/yr

Analyze stability data and trends to proactively identify risks, mitigate issues, and drive ... Minimum of 6+ years' experience - supporting Pharmaceutical Quality Control and Quality Assurance ...

NYCO PRODUCTS COMPANY

QC Chemist/Lab Tech

Countryside, IL · On-site

$21 - $23/hr

Perform stability testing on laboratory and manufacturing samples. * Communicate with outside ... Lab Technician/QC Chemist Qualifications: * Associate degree with an emphasis in Chemistry; or one ...

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All JobsQuality Control Stability JobsQuality Control Stability Jobs in Chicago, IL

Quality Control Stability information

See Chicago, IL salary details

$31.4K

$83.8K

$133.4K

How much do quality control stability jobs pay per year?

As of Aug 2, 2026, the average yearly pay for quality control stability in Chicago, IL is $83,775.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,300.00 and $103,000.00 per year, depending on experience, location, and employer.

What career paths are possible in QC?

Career paths in Quality Control (QC) include roles such as QC Technician, QC Analyst, Quality Assurance Specialist, and Quality Manager. Advancement often involves gaining experience, certifications like ASQ certifications, and developing skills in inspection, testing, and data analysis within manufacturing, pharmaceuticals, or food industries.

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

Which pays more, QA or QC?

In the field of Quality Control Stability, Quality Assurance (QA) roles generally offer higher salaries than Quality Control (QC) positions due to their broader responsibilities and focus on process improvement. QA jobs often require more experience and may involve certifications like Six Sigma or ISO standards, which can also influence pay. However, salaries vary based on industry, location, and level of experience.

What are some common challenges faced in a Quality Control Stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What are the key skills and qualifications needed to thrive as a Quality Control Stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What is a Quality Control Stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

Is QC analyst a stressful job?

A QC analyst role involves inspecting and testing products to ensure quality standards are met, which can be demanding during tight deadlines or when addressing product issues. The job often requires attention to detail, adherence to safety protocols, and sometimes working in environments with strict regulatory requirements, which can contribute to stress levels.

What is quality control salary?

The salary for a quality control stability role typically ranges from $40,000 to $70,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced professionals with certifications can earn higher wages. Salaries often include benefits such as health insurance and paid time off.
What are the most commonly searched types of Quality Control Stability jobs in Chicago, IL? The most popular types of Quality Control Stability jobs in Chicago, IL are:
What are popular job titles related to Quality Control Stability jobs in Chicago, IL? For Quality Control Stability jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability jobs in Chicago, IL look for? The top searched job categories for Quality Control Stability jobs in Chicago, IL are:
What cities near Chicago, IL are hiring for Quality Control Stability jobs? Cities near Chicago, IL with the most Quality Control Stability job openings:
Quality Control Stability jobs near you

Quality Control (QC) Analyst II

Kashiv Biosciences LLC

Chicago, IL • On-site

$24.75 - $33.25/hr

Full-time

Posted 27 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.

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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