Quality Assurance Associate (Pompano Beach, FL)

Client is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical manufacturing and drug development activities in a GMP-regulated environment. This is a great opportunity for individuals looking to begin their careers in biotech, particularly in quality and regulatory compliance.

Key Responsibilities :

• Receive and qualify incoming materials and reagents according to GMP requirements
• Review batch records, laboratory notebooks, and QC testing results for completeness and compliance
• Assist in deviation investigations and document change control processes
• Support the organization and maintenance of the electronic document control system
• Ensure compliance with internal SOPs and applicable cGMP regulations
• Participate in internal audits and prepare documentation for regulatory inspections
• Assist with data verification and archiving of quality-related records
• Contribute to creation and revisions of SOPs, forms, and controlled documents

Qualifications :