Quality Deviation Specialist III

**Quality Deviation Specialist III**Quality AssuranceSpringfield, Missouri, US+ Added - 10/02/2026Pay 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.**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 staffINDBHWe 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.