Real-Time QA Specialist – GMP & Compliance

August Bioservices; Tennessee; On-site; USD 65,000 - 95,000; Full time

Job summary

August Bioservices seeks a proactive QA Specialist to provide real‑time quality oversight across manufacturing, packaging, inspection, and warehouse operations in Nashville, TN. The ideal candidate ensures cGMP compliance, supports production activities, and guides operators to uphold quality standards.

With 2–5 years in a GMP environment and strong documentation practices, you will help maintain inspection readiness, facilitate deviations investigations, and support regulatory compliance.

Qualifications

• Bachelor's degree in a scientific discipline or equivalent experience.
• 2–5 years in a GMP-regulated environment with on‑the‑floor QA support.
• Knowledge of cGMPs, FDA/ICH regulations, and QA documentation practices.
• Familiarity with Master Control or electronic quality systems.

Responsibilities

• Provide real‑time QA support on the production floor and guide operators.
• Ensure adherence to batch records, SOPs, and validated procedures during manufacturing.
• Perform QA line clearances, in‑process checks, and AQL inspections.
• Assist in deviations, investigations, and CAPA processes as needed.

Skills

cGMP knowledge

FDA/ICH knowledge

QA documentation practices

Communication skills

GMP manufacturing presence

Education

Bachelor’s degree in a scientific discipline

Tools

Master Control

Job description

August Bioservices seeks a proactive QA Specialist to provide real‑time quality oversight across manufacturing, packaging, inspection, and warehouse operations in Nashville, TN. The ideal candidate ensures cGMP compliance, supports production activities, and guides operators to uphold quality standards.

With 2–5 years in a GMP environment and strong documentation practices, you will help maintain inspection readiness, facilitate deviations investigations, and support regulatory compliance.