Quality Assurance Specialist II​/III

Build your future at Curia, where our work has the power to save lives

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life‑saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.

• 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!

The Quality Assurance Specialist II/III serves as an embedded quality partner to manufacturing and laboratory operations, providing on‑floor oversight and proactive compliance support. This role is focused on identifying and mitigating compliance risks before and during production execution, driving adherence to cGMPs and internal procedures, and ensuring that when deviations occur, corrective actions are appropriate, timely, and thoroughly documented.

This position maintains and supports Curia’s Quality Management System across a broad range of activities, from document authorship, analytical data review, and audit participation to deviation management and client communication. The QA Specialist III applies strong knowledge of cGMP requirements, data integrity principles, and analytical laboratory practices, including chromatography, to evaluate records and data for accuracy, completeness, compliance, and scientific soundness.

The QA Specialist III is a self‑directed contributor who works collaboratively across departments to keep quality systems inspection‑ready and client timelines on track.

• Provide on‑floor QA oversight to manufacturing and laboratory operations, proactively identifying compliance risks and coordinating day‑to‑day quality activities as needed.
• Represent Curia Quality Assurance when issues require immediate corrective action, ensuring actions taken are appropriate and correctly documented to support traceability and investigation substantiation.
• Assist in or lead deviation and investigation processes, including initiation, immediate corrective action, root cause evaluation, and resolution.
• Track and follow up on Deviations, Change Controls, Investigations, and CAPAs to ensure timely closure.
• Actively participate in quality improvement initiatives, including development and implementation.

• Author, revise, review, and approve Quality Management System documents, including SOPs, CAPAs, Deviations, Change Controls, test methods, protocols, validation documentation, certificates of analysis, and equipment qualification documentation.
• Support compilation and maintenance of quality documentation and systems to ensure inspection readiness for domestic and international regulatory bodies (ISO, FDA, QP, EMEA).
• Develop, support, and maintain Quality System metrics for management review.
• Assist in training personnel in cGMPs, data integrity expectations, and Curia’s quality system to ensure real‑time compliance.
• Perform or support QA review of analytical data and associated documentation to verify accuracy, completeness, traceability, compliance with approved methods and procedures, and adherence to cGMP and data integrity requirements.
• Review analytical data generated through chromatography and other laboratory techniques, including associated chromatograms, calculations, audit trails, and supporting documentation, as applicable to the assigned area.
• Evaluate analytical data and…