Quality Assurance Associate

We are seeking a detail-oriented QA Associate to support quality assurance activities in a regulated pharmaceutical environment. The role ensures compliance with GMP standards and product quality across manufacturing and documentation processes.

Key Responsibilities:

Review batch records, SOPs, and quality documentation for compliance with GMP guidelines Perform in-process and final product quality checks Support deviation, CAPA, and change control processes Assist in internal and external audits (FDA, WHO, etc.) Ensure adherence to regulatory and company quality standards Maintain accurate QA records and reports Collaborate with production, QC, and regulatory teams

Requirements:

Bachelor's degree in Pharmacy, Chemistry, Life Sciences, or related field Basic understanding of GMP, GDP, and pharmaceutical regulations Strong attention to detail and documentation skills Good communication and analytical abilities Ability to work in a regulated, compliance-driven environment

Preferred Skills:

Exposure to pharmaceutical manufacturing or QC/QA environment (internship/trainee experience preferred) Knowledge of regulatory guidelines (FDA, WHO, ICH) Familiarity with documentation systems and audit processes

Pay:

$20.00 - $30.00 per hour

Benefits:

Health insurance Paid time off Vision insurance

Work Location:

In person