About this opportunity
Astrix lists this QC Deviation Specialist III opportunity in springfield, Missouri. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Pay Rate Low: 45 | Pay Rate High: 47
QC Deviation Specialist III (Contract)
Location: Onsite | Springfield, MO (Greene County)
Pay: $45–$47/hour
Terms: Project-Based Contract (3–6+ months, with potential extension)
Our client, a leading global CDMO , is seeking an experienced QC Deviation Specialist III to support a high-impact quality initiative at their Springfield, Missouri site. This is a project-based, onsite contract role focused on leading and executing complex deviation and OOS investigations across Manufacturing and Quality Control.
If you’re a seasoned quality professional who thrives in regulated environments, enjoys digging into root cause, and can confidently guide others through investigations — this role is built for you.
What You’ll Be Doing
Lead and author Manufacturing and QC deviation investigations, ensuring thorough, compliant, and timely documentation
Perform root cause analyses (RCA) and define effective corrective and preventive actions (CAPAs)
Execute and draft Out-of-Specification (OOS) investigations in alignment with GMP and regulatory standards
Partner closely with Manufacturing, QC, and Quality Assurance teams to support investigations and drive closure
Provide coaching, mentoring, and guidance to investigators, including investigator qualification support
Review investigation data to identify trends, recurring issues, and continuous improvement opportunities
Support and strengthen the site’s Quality Management System (QMS)
Ensure all work complies with GMP, ISO, and applicable regulatory requirements
What We’re Looking For
10+ years of experience in Quality Systems Management with direct involvement in deviation and OOS investigations
Strong expertise in RCA methodologies and CAPA development and execution
Proven experience authoring high-quality investigations in a regulated manufacturing environment (pharma, biotech, medical device, CDMO, etc.)
Ability to work independently while collaborating cross-functionally
Excellent analytical, documentation, and communication skills
Bachelor’s degree in a scientific, engineering, or technical discipline preferred
Nice to Have
Hands-on experience with GMP regulations and FDA / ICH guidance
Experience with electronic quality systems (TrackWise, Veeva Vault, or similar)
Prior experience training or mentoring investigators or quality staff
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Worksite address
springfield, MO, 65897, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.