On-the-Floor QA Lead: Compliance & CAPA Expert

Curia; Springfield (MO); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Generous benefits

Paid training

Career advancement

Education reimbursement

401K with match

Learning platform

Job summary

Curia is seeking a Quality Assurance Specialist III in Springfield, MO to serve as an embedded quality partner on the manufacturing floor. You will provide on-the-floor QA oversight, drive compliance with cGMPs, and coordinate deviation investigations and CAPAs to ensure timely, well-documented actions.

Ideal candidates have a life sciences degree and 6–8 years of QA experience in regulated environments, with strong communication skills and experience with ICH/Q7-Q10 and 21 CFR.

Qualifications

• Bachelor's degree in Life Sciences or related field; industry experience may compensate in combination.
• 6–8 years QA experience in pharma/biotech/cGMP FDA-regulated industry.
• Strong familiarity with regulatory requirements (ICH Q7/9/10 or 21 CFR 210/211).

Responsibilities

• Provide on-the-floor QA oversight to manufacturing operations and identify compliance risks.
• Represent QA for immediate corrective actions with proper documentation for traceability.
• Lead or assist in deviation/investigation processes and CAPA tracking.

Skills

QA experience

Regulatory compliance

cGMP

Problem-solving

Communication skills

Education

Bachelor's degree in Life Sciences

Job description

Curia is seeking a Quality Assurance Specialist III in Springfield, MO to serve as an embedded quality partner on the manufacturing floor. You will provide on-the-floor QA oversight, drive compliance with cGMPs, and coordinate deviation investigations and CAPAs to ensure timely, well-documented actions.

Ideal candidates have a life sciences degree and 6–8 years of QA experience in regulated environments, with strong communication skills and experience with ICH/Q7-Q10 and 21 CFR.