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Quality Control Stability Jobs in Illinois (NOW HIRING)

NOW Health Group

QC LAB TECH II - 1ST SHIFT

Bloomingdale, IL · On-site

$20 - $25.25/hr

... products, prepackaged items, stability samples and other laboratory samples. * Performs ... PERFORMANCE ABILITY Demonstrated ability to perform all of the duties of the Quality Control Lab ...

NOW Health Group

QC LAB TECH II - 3rd shift

Bloomingdale, IL · On-site

$20 - $25.25/hr

... products, prepackaged items, stability samples and other laboratory samples. * Performs ... PERFORMANCE ABILITY Demonstrated ability to perform all of the duties of the Quality Control Lab ...

BISCO Dental Products

Quality Systems Manager

Schaumburg, IL · On-site

$110 - $129/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Oversee QC laboratory and receiving inspection activities, including raw material inspection, work‑in‑process inspection, stability monitoring, equipment, and related product trend analysis.

BISCO, Inc.

Quality Systems Manager

Schaumburg, IL · On-site

$110K - $129K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Oversee QC laboratory and receiving inspection activities, including raw material inspection, work-in-process inspection, stability monitoring, equipment, and related product trend analysis. * Lead ...

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All JobsQuality Control Stability JobsQuality Control Stability Jobs in Illinois

Quality Control Stability information

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.

Is quality control stability a good career path?

Quality control stability involves ensuring products meet quality standards over time, often requiring attention to detail and knowledge of testing procedures. It can offer steady employment and opportunities for advancement in manufacturing, pharmaceuticals, or food industries, especially for those with relevant certifications or experience. The role typically involves working in controlled environments and may require familiarity with quality management systems and inspection tools.

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.

What are the most commonly searched types of Quality Control Stability jobs in Illinois?

The most popular types of Quality Control Stability jobs in Illinois are:

What are popular job titles related to Quality Control Stability jobs in Illinois?

For Quality Control Stability jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Quality Control Stability jobs in Illinois look for?

The top searched job categories for Quality Control Stability jobs in Illinois are:

What cities in Illinois are hiring for Quality Control Stability jobs?

Cities in Illinois with the most Quality Control Stability job openings:

Quality Control Stability jobs near you

QC REVIEW SPECIALIST II

NOW Health Group

Bloomingdale, IL • On-site

Full-time

Re-posted 15 days ago

Job description

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
  • Performs detailed review of analytical and ICP test results generated by QC department for compliance with cGMP, internal SOPs and specifications to support production, stability studies, method development, QA, R&D and lab operation.
  • Performs detailed data review for analytical test results generated by contract testing labs to assure correctness and accuracy.
  • Coordinates with Method Development and/or Lab Management for resolution of any deviations from methods, discrepancies with specifications.
  • Reviews data and reports associated with method transfers and method validation.
  • Coordinates with multiple departments to obtain information for accurate sample review, such as product safety review and material qualification.
  • Provides information for investigative steps of laboratory non-conformances investigations and escalates any issues noted to management.
  • Communicates with management for timely resolution of invalid or problematic testing.
  • Performs and/or facilitates SOP review, revising and training.
  • Creates and/or reviews procedural SOP.
  • Initiates change process for any erroneous methods or specifications.
  • Updates spreadsheets to reflect status of reviewed data and metrics of errors, investigations and invalid runs; communicates status of priority runs in a timely manner.
  • Initiates and participates in process improvement activities.
  • Any special projects assigned by management.
  • Complies with all safety and GMP requirements.

SAFETY STATEMENT RESPONSIBILITY
Supports a culture of safe laboratory and production operations; follows all safety rules and procedures. Actively participates in the safety program by: engaging in training activities to learn what constitutes a safety hazard; reporting safety concerns to management or safety teams, submitting safety suggestions, and correcting or reporting to the appropriate people when the employee sees a workplace health or safety hazard, until it is resolved. Assists with communicating safety information to new employees. Fulfills responsibilities as outlined in the company safety management plan.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE
  • Bachelor's degree (B.S.) or equivalent from four-year College or technical school in a laboratory science such as Chemistry, Biology or related field.
  • At least four years of laboratory and/or QA/Regulatory compliance experience.
  • At least two year of instrumentation troubleshooting and/or training experience.
  • At least two years of data acquisition, interpretation and/or reporting experience.
  • Excellent computer skills required, including Microsoft Word, Access and Excel.
  • Experience with database management systems such as Oracle and LIMS are desired.
  • Strong working knowledge and application of cGMP regulations.

LANGUAGE SKILLS
  • Must be able to read and interpret documents such as complex analytical data, product specifications, departmental instructions, and procedure manuals.
  • Must be able to communicate and work with peers and management in a transparent and professional manner.

MATHEMATICAL SKILLS
  • Ability to apply concepts such as fractions, percentages, averages, ratios, proportions, and the metric system to practical situations.

REASONING ABILITY
  • Must be able to compare results obtained to specifications to determine if result meets requirements.
  • Must be able to gather, generate and interpret data and a variety of instructions.

OTHER SKILLS AND ABILITIES
  • Knowledge of industry quality control procedures, chemical laboratory instrumentation, standard operating procedures and compliance experience required.
  • Excellent time management, meeting deadlines, attention to detail, verbal and written communication skills, listening, decision-making, troubleshooting/problem solving and organization skills required.
  • Must be a self-starter and able to handle multiple tasks.

PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to sit/stand, write, type, talk and hear. The employee frequently is required to stand, walk, and reach with hands and arms. The employee is required to regularly use a telephone, a computer and analytical instrumentation and devices. The employee must frequently lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
The employee is frequently exposed to vapors and/or herbal aromas. The noise level in the work environment is usually moderate. The employee may be exposed to potentially hazardous chemicals and biological materials. Safety training and personal protective equipment are available and required.
2025 BENEFITS AT A GLANCE
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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