Quality Investigations Specialist III

Job overview

The Quality Investigations Specialist III role is onsite in Albuquerque, NM. Compensation is not specified. The position provides Quality Assurance oversight for Curia’s pharmaceutical manufacturing operations and supports product quality, patient safety, and regulatory compliance. The specialist leads and reviews investigations into deviations, non-conformances, complaints, and other quality issues. Through root-cause analysis, corrective and preventive actions, audit support, and process improvements, the role helps maintain compliant and robust manufacturing processes.

What you'll do

• Provide QA oversight and subject-matter expertise for GMP investigations
• support product complaints, deviations, and failure investigations
• review and close deviation investigations, CAPAs, and related change controls
• support root-cause analysis and corrective actions
• identify procedural deficiencies and propose solutions
• revise, review, and approve SOPs independently
• mentor team members
• support FDA and other agency inspections and customer and internal audits
• participate in site or global improvement projects as needed.

What we're looking for

Skills & competencies

quality investigations specialist iii

quality assurance

gmp investigations

root cause analysis

capa

pharmaceutical manufacturing

albuquerque nm

curia

fda inspections

sops

audit readiness

full-time

Work arrangement

• Weekend coverage required

Benefits & perks

• Benefit options from the first day of employment, paid training, vacation and holidays, career advancement opportunities, education reimbursement, 401(k) matching contributions, and a learning platform.

Why this role

Requires a bachelor’s degree in a relevant science field and at least five years of relevant pharmaceutical quality assurance and/or regulatory experience.

About the employer

Curia is hiring for this role. Industry: Pharmaceutical Preparation Manufacturing. Sector: 32.