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Quality Assurance Risk Manager Jobs in Springfield, MO

Partner with Manufacturing, Quality Assurance, Engineering, Maintenance, and other teams to resolve ... Risk of electrical shock may be present. The employee will help manage handling of hazardous waste ...

Partner with Manufacturing, Quality Assurance, Engineering, Maintenance, and other teams to resolve ... Risk of electrical shock may be present. The employee will help manage handling of hazardous waste ...

Showing results 41-60

Quality Assurance Risk Manager information

See Springfield, MO salary details

$34.6K

$107.4K

$162.8K

How much do quality assurance risk manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for quality assurance risk manager in Springfield, MO is $107,403.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $131,400.00 per year, depending on experience, location, and employer.

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

AspectQuality Assurance Risk ManagerQuality Control Specialist
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentRisk assessment, process improvement, complianceProduct inspection, testing, defect identification
Industry UsageManufacturing, healthcare, aerospaceManufacturing, food production, electronics

The Quality Assurance Risk Manager focuses on identifying and mitigating risks in processes to ensure quality standards are met, often involving risk assessments and compliance. In contrast, the Quality Control Specialist primarily conducts product inspections and tests to detect defects. Both roles require similar certifications and are integral to quality management but differ in scope and focus.

What is quality assurance in risk management?

In the context of a Quality Assurance Risk Manager, quality assurance in risk management involves systematically identifying, assessing, and mitigating potential risks that could impact product quality or operational processes. It includes implementing standards, conducting audits, and using tools like risk assessments to ensure compliance and reduce errors, thereby maintaining product integrity and customer satisfaction.

What cities near Springfield, MO are hiring for Quality Assurance Risk Manager jobs?

Cities near Springfield, MO with the most Quality Assurance Risk Manager job openings:

QC Deviation Specialist III

Astrix Technology

Springfield, MO

$45 - $47/hr

Contractor

Posted 20 days ago


Job description

QC Deviation Specialist III

Quality Control

Springfield, Missouri, US

  • Added - 12/11/2025

Our client, a leading global CDMO, is looking to hire a QC Deviation Specialist III to join their growing team in Greene County, Missouri!

Pay rate: $45 -$47/hr.

Location: Greene County, Missouri

Job type : 4-month contract (possibility of extension)

Position Summary

The QC Deviation Specialist III will be responsible for leading and executing quality investigations, including deviations and OOS events, within Manufacturing and QC departments. This role ensures compliance with internal procedures, regulatory requirements, and industry best practices while driving continuous improvement through effective root cause analysis (RCA) and implementation of corrective and preventive actions (CAPAs).

Key Responsibilities

  • Perform and document Deviation Investigations for Manufacturing and Quality Control operations.
  • Conduct Root Cause Analyses (RCA) and determine appropriate Corrective and Preventive Actions (CAPAs) to address identified issues.
  • Partner with Manufacturing, QC, and Quality Assurance teams to support investigations and ensure timely and compliant closure.
  • Provide coaching and training to staff on deviation investigations, RCA methodologies, and investigator qualification.
  • Perform and draft Out-of-Specification (OOS) investigations in accordance with internal policies and regulatory standards.
  • Review and analyze data to identify trends, recurring issues, and opportunities for process improvement.
  • Support continuous improvement initiatives within the Quality Management System (QMS).
  • Ensure all activities comply with applicable GMP, ISO, and regulatory requirements.

Qualifications

  • Minimum 10 years of relevant experience in Quality Systems Management, with direct experience in manufacturing and quality control deviation management.
  • Strong knowledge of Root Cause Analysis (RCA) and CAPA development and implementation.
  • Proven experience writing and managing quality investigations in a regulated industry (e.g., pharmaceutical, biotechnology, medical device, or similar).
  • Bachelor's degree preferred in a scientific, engineering, or related technical discipline.
  • Excellent analytical, problem-solving, and communication skills.
  • Ability to work independently and collaboratively in a cross-functional team environment.

Preferred Qualifications

  • Familiarity with Good Manufacturing Practices (GMP) and regulatory guidance (e.g., FDA, EMA, ICH).
  • Experience using electronic quality systems (e.g., TrackWise, Veeva Vault, or similar).
  • Prior experience mentoring or training personnel on deviation and CAPA processes.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.