Senior QA Specialist III – On‑Floor Compliance & Data Integrity

Curia Aalborg ApS; Springfield (MO); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Career advancement

Education reimbursement

401K program

Learning platform

Paid training

Generous benefit options

Job summary

Curia is seeking a Quality Assurance Specialist II/III in Springfield, MO to serve as an embedded partner with manufacturing and laboratory operations, driving cGMP compliance and timely documentation.

You will lead deviation investigations, support audits, and maintain QA documentation, ensuring traceability and adherence to data integrity and cGMP standards. A bachelor's in Life Sciences and 3–8 years QA experience are required.

Qualifications

• Bachelor's degree required in Life Sciences or related field.
• 3–6 years (Level II) or 6–8 years (Level III) QA/QC/analytical lab or related quality experience in regulated industry.
• Experience reviewing analytical data in cGMP environments with data integrity and good documentation practices.

Responsibilities

• Provide on-floor QA oversight to manufacturing and laboratory operations to identify compliance risks.
• Lead or assist deviation and investigation processes with root cause analysis.
• Track Deviations, Change Controls, Investigations, and CAPAs for timely closure.
• Participate in audits and client communications; support QA in ensuring timelines.
• Maintain QA documentation and participate in training on cGMP and data integrity.

Skills

QA/compliance

cGMP

Data integrity

HPLC/GC

Documentation

Regulatory knowledge

Communication

Problem solving

MS Office

Education

Bachelor's degree in Life Sciences or related field

Tools

Microsoft Office

Job description

Curia is seeking a Quality Assurance Specialist II/III in Springfield, MO to serve as an embedded partner with manufacturing and laboratory operations, driving cGMP compliance and timely documentation.

You will lead deviation investigations, support audits, and maintain QA documentation, ensuring traceability and adherence to data integrity and cGMP standards. A bachelor's in Life Sciences and 3–8 years QA experience are required.