Quality Assurance Specialist - Springfield, MO
Listed on 2025-10-31
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Quality Assurance - QA/QC
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Healthcare
Data Scientist
Overview
Quality Assurance Specialist I - Springfield, MO
Join to apply for the Quality Assurance Specialist I - Springfield, MO role Description available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. This role is On-Site at the location detailed in the job post. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies.
Quality Assurance Specialist I in Springfield, MO. Build your future at Curia, where our work has the power to save lives.
Responsibilities- Maintain Quality databases including Archival and scanning of cGMP documents and records, Departures, media fill programs, and training files
- Represent Curia Quality Assurance when managing issues that require immediate corrective action. Ensure such action taken is appropriate and correctly documented
- Solicit feedback from various departments for operational improvement
- Author, review, and/or approve Quality Management System documents, including, but not limited to, change controls, SOPs, deviations, CAPAs, etc.
- Assist in performing investigations
- Perform and/or assist with internal audits, weekly walkthroughs, and/or external audits
- Perform QA visual inspection activities associated with clinical and commercial drug product
- With supervision, may respond or manage responses to clients regarding manufacturing and/or documentation issues
- Develop and/or maintain Quality System metrics for management review
- Assist in tracking and follow-up on Deviations, Change Controls, Investigations, and CAPAs
- Minimum
Education Required:
High School/GED - Additional Qualifications/Responsibilities:
Bachelor’s degree in Life Science or related field. Directly related experience in a GMP environment may augment degree requirements. - Minimum 0-3 years’ experience in a cGMP and FDA-regulated industry
- Prior Experience In a GMP Regulated Environment Preferred
- Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
- Supervisory responsibilities:
This position does not have supervisory responsibilities.
- City:
Springfield - State:
Missouri - Job Code:
Manufacturing Manufacturing - Affiliate Sponsor:
Curia
- Generous benefit options (eligible first day of employment)
- Paid training, vacation and holidays (vacation accrual begins on first day of employment)
- Career advancement opportunities
- Education reimbursement
- 401K program with matching contributions
- Learning platform
- And more!
- Seniority level:
Entry level - Employment type:
Full-time - Job function:
Quality Assurance
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