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Quality Control Investigator Jobs in Springfield, MO

Astrix Inc

QC Deviation Specialist III

Springfield, MO · On-site

$45 - $47/hr

Perform and document Deviation Investigations for Manufacturing and Quality Control operations. * Conduct Root Cause Analyses (RCA) and determine appropriate Corrective and Preventive Actions (CAPAs ...

Astrix Inc

QA Specialist III

Springfield, MO · On-site

$45 - $47/hr

Perform and document Deviation Investigations for Manufacturing and Quality Control operations. * Conduct Root Cause Analyses (RCA) and determine appropriate Corrective and Preventive Actions (CAPAs ...

AllSTEM Connections

Quality Specialist

Springfield, MO · On-site

$93K/yr

Lead and draft comprehensive investigations for deviations occurring within both Manufacturing and Quality Control (QC) departments. Root Cause & CAPA: Utilize structured methodologies to perform ...

OWN, Inc.

Team Leader - Field Services

Springfield, MO · On-site

$13.50 - $17.75/hr

Implement and enforce company standards, QA/QC procedures, and quality control processes on all ... geotechnical investigations, materials testing procedures, environmental assessments, and/or ...

QPS

Clinical Pharmacist

Springfield, MO · On-site

$107K - $128K/yr

... Investigator. * Execute clinical trials in compliance with study protocols, Good Clinical Practice (GCP), FDA regulations, QA/QC procedures, OSHA guidelines, and applicable state and local ...

QPS, LLC

Clinical Pharmacist

Springfield, MO · On-site

$111K - $133K/yr

... Investigator. * Execute clinical trials in compliance with study protocols, Good Clinical Practice (GCP), FDA regulations, QA/QC procedures, OSHA guidelines, and applicable state and local ...

Luxus

Senior Structural Project Manager

Springfield, MO

$85K - $116K/yr

Conduct site investigations, condition assessments, and construction observations. * Serve as ... Manage multiple projects simultaneously, including scope, schedule, budget, and quality control.

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Quality Control Investigator information

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How much do quality control investigator jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for quality control investigator in Springfield, MO is $19.53, according to ZipRecruiter salary data. Most workers in this role earn between $15.72 and $21.88 per hour, depending on experience, location, and employer.

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

To thrive as a Quality Control Investigator, you need expertise in quality assurance processes, attention to detail, and a background in science or engineering, often supported by relevant certifications such as Six Sigma or ISO compliance. Familiarity with laboratory equipment, statistical analysis software, and quality management systems is typically required. Strong analytical thinking, problem-solving abilities, and effective communication are essential soft skills in this role. These competencies ensure that products and processes consistently meet regulatory standards and company expectations, minimizing errors and maintaining organizational integrity.

What are some common challenges faced by quality control investigators, and how can they be addressed?

Quality Control Investigators often encounter challenges such as managing tight deadlines for investigating quality deviations, ensuring thorough documentation, and coordinating with multiple departments to collect necessary information. To address these, it's important to develop strong organizational skills, maintain clear communication channels, and stay current with regulatory requirements. Proactively collaborating with production, QA, and regulatory teams can help streamline investigations and lead to more effective root cause analysis and corrective actions.

What is the difference between Quality Control Investigator vs Quality Assurance Specialist?

AspectQuality Control InvestigatorQuality Assurance Specialist
CertificationsOften requires GMP, GLP, or ISO certificationsSimilar certifications, with additional focus on auditing
Work EnvironmentLaboratory, manufacturing, or production settingsOffice, laboratory, or production environments
Primary FocusInvestigating quality issues, deviations, and non-conformancesDeveloping and implementing quality systems and procedures
Employer & Industry UsagePharmaceutical, biotech, manufacturingPharmaceutical, biotech, manufacturing

Both roles are vital in quality management, but the Quality Control Investigator primarily focuses on identifying and resolving quality issues through investigations, while the Quality Assurance Specialist develops systems to prevent issues. They often work together to ensure product quality and compliance.

What is a quality control investigator?

Quality Control Investigators are professionals responsible for ensuring that products or services meet established quality standards and regulatory requirements. They inspect processes, materials, and finished goods, investigate quality issues, and recommend corrective actions to prevent recurrence. Their work is crucial in maintaining product safety, consistency, and compliance across various industries, such as manufacturing, pharmaceuticals, and food processing.
What are popular job titles related to Quality Control Investigator jobs in Springfield, MO? For Quality Control Investigator jobs in Springfield, MO, the most frequently searched job titles are:
Quality Control Investigator jobs near you
Infographic showing various Quality Control Investigator job openings in Springfield, MO as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $40,631 per year, or $19.5 per hour.

QC Deviation Specialist III

Astrix Inc

Springfield, MO • On-site

$45 - $47/hr

Contractor

Re-posted 26 days ago

Job description

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.

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