Senior QA Specialist — cGMP Compliance

Curia Global, Inc.; Camarillo, Northern (CA, KY); Hybrid; USD 91,000 - 114,000; Full time

Benefits offered by this job

Generous benefit options

Paid training

Career advancement opportunities

Education reimbursement

401K program with matching

Learning platform

And more!

Job summary

Curia Global, Inc. in Camarillo, CA seeks a Quality Assurance (QA) Specialist III to uphold quality systems in cGMP production. You will review records, manage deviations, CAPAs, and change controls while coordinating with multiple functions to ensure timely, compliant execution.

The role emphasizes training, SOP authoring, and supporting regulatory audits. A Bachelor’s degree with 5+ years of GMP/QA experience in FDA-regulated pharma is required.

Qualifications

• Bachelor’s Degree with a minimum of 5 years’ GMP and QA experience in an FDA-regulated environment.
• Experience reviewing batch records, deviation investigations, CAPAs, and change controls.
• Ability to develop and deliver training and author SOPs.

Responsibilities

• Work cross-functionally with Manufacturing, Process Engineering and Technical Operations to support Right First-Time execution.
• Review batch records, QC data, and environmental monitoring for compliance and disposition.
• Review and approve procedural changes and validation documentation.
• Attend client meetings and manage responses to manufacturing or documentation issues.
• Develop metrics for Management Review and assist audits for ISO, FDA and other bodies.

Skills

QA experience

GMP experience

FDA regulation knowledge

Quality Systems

Communication skills

Education

Bachelor's Degree

Job description

Curia Global, Inc. in Camarillo, CA seeks a Quality Assurance (QA) Specialist III to uphold quality systems in cGMP production. You will review records, manage deviations, CAPAs, and change controls while coordinating with multiple functions to ensure timely, compliant execution.

The role emphasizes training, SOP authoring, and supporting regulatory audits. A Bachelor’s degree with 5+ years of GMP/QA experience in FDA-regulated pharma is required.