Global GMP Compliance Auditor - Audit CAPA & Readiness

Efficientauditing; Chicago (IL); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Professional development opportunities

Supportive team culture

High-impact projects

Job summary

A regulatory compliance firm is seeking a GMP Compliance Auditor in Chicago, IL, to evaluate and ensure adherence to Good Manufacturing Practices across various life-science sectors. The ideal candidate will possess 3-7 years of extensive auditing experience and a relevant degree. Responsibilities include conducting audits, assessing regulatory compliance, and providing CAPA guidance. Join our collaborative team to work on impactful projects enhancing product quality and patient safety.

Qualifications

• 3–7 years of experience in GMP auditing, compliance, or quality assurance.
• Strong understanding of pharmaceutical manufacturing requirements and quality systems.
• Excellent report writing and communication skills.

Responsibilities

• Conduct GMP audits for clients including facility and documentation evaluations.
• Assess compliance with FDA, EMA, WHO regulations.
• Identify non-conformities and improvement opportunities.

Skills

GMP auditing

Regulatory compliance

Analytical skills

Report writing

Communication skills

Education

Bachelor’s or Master’s degree in Pharmacy, Biotechnology, Life Sciences, Engineering

Job description

A regulatory compliance firm is seeking a GMP Compliance Auditor in Chicago, IL, to evaluate and ensure adherence to Good Manufacturing Practices across various life-science sectors. The ideal candidate will possess 3-7 years of extensive auditing experience and a relevant degree. Responsibilities include conducting audits, assessing regulatory compliance, and providing CAPA guidance. Join our collaborative team to work on impactful projects enhancing product quality and patient safety.