Quality Assurance Specialist: GMP & Documentation

ezlifepharma; Atlanta (GA); On-site; USD 50,000 - 70,000; Full time

Job summary

A reputable pharmaceutical company in Atlanta is seeking a meticulous Quality Assurance Associate to ensure products meet quality and regulatory standards. The successful candidate will review documentation, conduct inspections, and maintain GMP compliance, contributing significantly to quality assurance efforts. This role presents a great opportunity for individuals with a background in life sciences who aim to progress in a QA career.

Qualifications

• Bachelor’s Degree required in a related field.
• 1–3 years experience in QA preferred.
• Familiarity with GMP/ISO standards essential.

Responsibilities

• Review and approve production and QC documentation.
• Conduct quality checks on in-process and finished products.
• Coordinate product stability studies and oversee raw material verification.

Skills

Documentation

Analytical Skills

Knowledge of GMP/ISO Standards

Education

Bachelor’s Degree in Pharmacy, Chemistry, or Life Sciences

Tools

QA Software/Tools

Job description

A reputable pharmaceutical company in Atlanta is seeking a meticulous Quality Assurance Associate to ensure products meet quality and regulatory standards. The successful candidate will review documentation, conduct inspections, and maintain GMP compliance, contributing significantly to quality assurance efforts. This role presents a great opportunity for individuals with a background in life sciences who aim to progress in a QA career.