Quality Assurance Specialist II-III

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

Job Description
Quality Assurance Specialist III – Springfield, MO

Job Description
Quality Assurance Specialist III – Springfield, MO
Build your future at Curia, where our work has the power to save lives.

The Quality Assurance Specialist III serves as an embedded quality partner to manufacturing operations, providing on-the-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 and audit participation to deviation management and client communication. 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.

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.

We proudly offer

• 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!

Responsibilities

Floor Presence and Compliance

• Provide on-the-floor QA oversight to manufacturing 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, 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.

Quality Systems and Documentation

• 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 and Curia’s quality system to ensure real-time compliance.

Audits and Client Support

• Participate in and support internal and external audit programs, including planning, conducting audits, weekly walkthroughs, and preparing audit reports.
• Participate in regulatory, client, and external supplier qualification audits.
• With appropriate supervision, respond to or manage client communications regarding manufacturing, testing, and documentation issues.
• Support QA team members and internal project teams to ensure client timelines are on schedule, communicating proactively with customer contacts as needed.
• Report personnel performance observations to appropriate management, noting both areas for improvement and individuals exceeding expectations.

Good Manufacturing & Documentation Practices

Quality is something we take pride in together. You’ll perform your work in alignment with cGMP requirements and Curia’s standards to ensure our facilities support the safe and reliable manufacture of products for our customers.

• Perform all documentation in compliance with ALCOA++ principles and site SOPs.
• Adhere to applicable cGMP documents including SOPs, batch records, protocols, change controls, and controlled forms.
• Keep all required cGMP training current and escalate quality concerns along with proposed solutions to the Quality department.

Required

• Bachelor’s degree in Life Sciences or a related field; alternate fields of study may be considered in combination with significant industry experience
• Minimum 6–8 years of QA experience in pharmaceutical, biotechnology, medical device, or a cGMP FDA-regulated industry
• Strong familiarity with regulatory requirements including ICH Q7, Q9, Q10, and/or 21 CFR 210 and 211
• Excellent written and verbal communication skills, including the ability to present information clearly to management and peers
• Strong problem-solving and conflict resolution skills
• Ability to work independently and proactively while collaborating effectively across departments
• Detail-oriented, self-directed, and comfortable managing multiple priorities simultaneously
• Working knowledge of Microsoft Office or other relevant software

Preferred

• Experience working with third-party contract manufacturing in the pharmaceutical industry

Other Qualifications

• Must pass a background check
• Must pass a drug screen
• May be required to pass Occupational Health Screening
• May be required to obtain and maintain gowning certification
• May be required to obtain and maintain media qualification

Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.

All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.