QA Specialist II - cGMP & Data Integrity

Curia Aalborg ApS; Springfield (AL); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Generous benefits (eligible first day)

Paid training

Vacation and holidays

Career advancement opportunities

Education reimbursement

401K with matching

Learning platform

Job summary

Curia is seeking a Quality Assurance Specialist II to provide on-the-floor QA oversight in Springfield, MO. You will review data and documentation, support investigations, and ensure adherence to cGMP and data integrity standards across manufacturing and lab operations.

Ideal candidates have 3–6 years of QA or related FDA-regulated experience, strong analytical and communication skills, and proficiency with electronic quality systems and Microsoft Office.

Qualifications

• Bachelor’s degree in Life Science, Chemistry, Biology, or related field.
• 3–6 years of QA/QC or FDA-regulated experience.
• Experience reviewing cGMP documentation and analytical data.
• Knowledge of FDA regulations, cGMP, and ALCOA+.
• Ability to identify and escalate compliance concerns.
• Strong written and verbal communication and teamwork.
• Proficiency with Microsoft Office and electronic quality systems.

Responsibilities

• Provide on-the-floor QA oversight to manufacturing operations and document deviations.
• Review QC data, batch records, and cGMP documents for accuracy and completeness.
• Support investigations, CAPAs, and change controls with rigorous data review.
• Collaborate across functions to ensure real-time compliance and quality events resolution.
• Participate in internal and client audits and regulatory inspections.
• Maintain quality system records and training documentation.

Skills

Quality Assurance

cGMP

Data integrity

Analytical thinking

Documentation

Communication

Education

Bachelor’s degree in Life Science, Chemistry, Biology, or related field

Tools

Microsoft Office

LIMS/ELN systems

Job description

Curia is seeking a Quality Assurance Specialist II to provide on-the-floor QA oversight in Springfield, MO. You will review data and documentation, support investigations, and ensure adherence to cGMP and data integrity standards across manufacturing and lab operations.

Ideal candidates have 3–6 years of QA or related FDA-regulated experience, strong analytical and communication skills, and proficiency with electronic quality systems and Microsoft Office.