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QC Deviation Specialist III
Job in
Springfield, Greene County, Missouri, 65897, USA
Listed on 2026-02-15
Listing for:
Astrix
Full Time
position Listed on 2026-02-15
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst
Job Description & How to Apply Below
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
- 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
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