Quality Deviation Specialist III

Quality Deviation Specialist III

Quality Assurance

Springfield, Missouri, US

Pay Rate Low: 45 | Pay Rate High: 47

QC/QA 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.

• 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

• 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

• Hands‑on experience with GMP regulations and FDA / ICH guidance
• Experience with electronic quality systems (Track Wise, Veeva Vault, or similar)
• Prior experience training or mentoring investigators or quality staff

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.