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Manager Quality Risk Jobs in Chicago, IL (NOW HIRING)

Assertio Therapeutics

Manager, QA

Lake Forest, IL · On-site

Perform risk analysis to assess inadvertent events that may impact product identity, strength, quality, purity. * Advise and/or manage risk management strategies. * Author quality agreements and ...

Assertio Therapeutics

Manager, QA

Lake Forest, IL · On-site

Perform risk analysis to assess inadvertent events that may impact product identity, strength, quality, purity. * Advise and/or manage risk management strategies. * Author quality agreements and ...

Assertio Therapeutics

Manager, QA

Lake Forest, IL · On-site

Perform risk analysis to assess inadvertent events that may impact product identity, strength, quality, purity. * Advise and/or manage risk management strategies. * Author quality agreements and ...

Jobtailor

Manager, QA Compliance

Melrose Park, IL · On-site

$125 - $150/hr

Perform or assist with supplier risk assessments for non-compliance inspection outcomes ... Coordinate and manage Global Procurement Quality Agreement database updates and reviews

New

Fresenius Kabi

Manager, QA Compliance

Melrose Park, IL · On-site

Job Summary The Manager, QA Compliance is responsible for supporting the company's short and ... Perform or assist with supplier risk assessment for non-compliance (i.e. FDA WL, etc.) inspection ...

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All JobsQuality Risk JobsManager Quality Risk JobsManager Quality Risk Jobs in Chicago, IL

Manager Quality Risk information

See Chicago, IL salary details

$24.7K

$88.8K

$162.8K

How much do manager quality risk jobs pay per year?

As of Sep 9, 2026, the average yearly pay for manager quality risk in Chicago, IL is $88,757.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,300.00 and $140,100.00 per year, depending on experience, location, and employer.

What is the difference between Manager Quality Risk vs Quality Assurance Manager?

AspectManager Quality RiskQuality Assurance Manager
Primary FocusIdentifying and mitigating quality risks across processesEnsuring products/services meet quality standards through testing and audits
CertificationsISO 9001, Six Sigma, Risk Management certificationsISO 9001, Six Sigma, Quality Management certifications
Work EnvironmentCross-departmental risk assessments, compliance teamsQuality labs, production lines, audit teams
Industry UsageManufacturing, healthcare, financeManufacturing, software, healthcare

While both roles focus on quality, the Manager Quality Risk primarily concentrates on identifying and managing potential risks to quality, whereas the Quality Assurance Manager ensures that products or services consistently meet quality standards through testing and process audits.

What does a Manager Quality Risk do?

A Manager of Quality Risk oversees the identification, assessment, and mitigation of risks related to product quality and compliance within an organization. They develop risk management strategies, ensure adherence to industry standards, and often utilize tools like risk assessment matrices and quality management systems. This role typically requires strong analytical skills, knowledge of regulatory requirements, and relevant certifications such as Six Sigma or ISO standards.
Manager Quality Risk jobs near you

Manager, Quality Operations

Portage, IN • On-site

Aquestive Therapeutics
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Aquestive Therapeuticsexternal

Full-time

Re-posted 5 hours ago

Job description

Job Summary:

Responsible for leading day-to-day quality oversight of manufacturing and operational activities to ensure compliance with cGMP, regulatory requirements, and company quality systems. Drives execution, inspection readiness, and continuous improvement across quality operations.

This position will be expected to work in a highly collaborative, cross functional team environment, and provide expert knowledge to risk identification/mitigation, strategy and execution. 

Responsibilities:
  • Daily GMP Oversight (Shop Floor + Operations), providing real-time QA oversight of manufacturing and packaging activities of a multi-site, multi-shift operation.
  • Manage the product quality release program, ensuring on-time results and adherence to internal procedures.
  • Provide quality risk assessment and decision support real-time, including containment correction measures.
  • Review and release of batch records.
  • Author, review and/or approve quality documentation related to manufacturing.
  • Ensure adherence to SOPs, batch records, and GMP requirements
  • Lead and/or oversee deviations, OOS, complaints, and investigations, ensuring robust root cause analysis and effective CAPAs.
  • Manage Quality Operations personnel, setting priorities, staffing plans and shift coverage.
  • Manage incoming materials quality review/approval to ensure materials are appropriately received, assessed, and released for use in accordance with applicable procedures.
  • Coach team on GMP decision-making, risk-based quality judgement and investigator rigor.
  • Monitor and report key quality metrics, including right first time.
  • Identify trends and drive process improvements and simplification.
  • Ensure continuous state of audit readiness, supporting health authority inspections and internal audits.
  • Act as a primary QA partner to Manufacturing, Quality Control and Supply Chain and Quality Systems.

Qualifications:

          • Education: Bachelor’s degree (Science, Engineering, or related)
          • Experience: ~7–10 years in GMP pharmaceutical manufacturing QA/QC
          • Leadership: Prior people management or strong informal leadership
          • Expertise:
            • cGMP regulations (FDA / EU)
            • Quality systems (CAPA, deviations, change control)
            • Manufacturing and/or QC operations
          • Excellent computer skills required (e.g., Microsoft Word, Excel, Access, PowerPoint, Visio).
          • Strong project management skills, strong organizational skills to maintain a high level of productivity, innovation, and priority-setting to complete assignments on time and on budget.
          • Strong business acumen surrounding pharmaceutical manufacturing.
          • Some travel required.

           

          The above statements are intended to describe the general nature and level of the work being performed by colleagues assigned to this position. This is not intended to be an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary.

          As part of Aquestive’s employment process, final candidate will be required to complete a drug test and background check prior to employment commencing.  Please Note:  Aquestive is a drug-free workplace and has a drug free workplace policy in place.

          Aquestive provides equal employment opportunities to all colleagues and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

          The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.

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