Quality Assurance Specialist in Pharmaceuticals

Elevate product integrity as a Quality Assurance Specialist in the pharmaceutical industry. Review and release goods while ensuring compliance with regulations and specifications.

This position involves critical tasks for the Quality Assurance team, including reviewing bulk materials, initiating deviation investigations, and supporting internal audits. The role requires a strong understanding of cGMP, FDA regulations, and quality monitoring processes to ensure continuous improvement and compliance.

Key Responsibilities:

• Review and release bulk and finished goods for compliance

• Initiate and investigate deviations and corrective actions

• Monitor process performance to drive improvements

• Review specifications and formulas in LIMS

• Support quality audits and complete APQR reports

Requirements:

• Bachelor’s degree in Microbiology, Biology, or Chemistry

• 3-5 years in QA within pharmaceuticals or dietary supplements

• Knowledge of FDA
21CF
R111 and USP regulations

• Hands-on experience in manufacturing environments

• Proficiency in MS Office and data entry

Bring your QA expertise and regulatory knowledge to maintain high quality standards in the pharmaceutical industry.
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