Quality Assurance Specialist

Quality Assurance Specialist / QA Specialist

Location: Sanford, FL

Step into a pivotal role where your work directly safeguards product quality and patient safety. As a key contributor within my client’s Quality team, you’ll drive compliance, elevate quality systems, and ensure operational excellence across critical pharmaceutical processes. This is your opportunity to make a measurable impact in a highly regulated, mission-driven environment.

Why You Should Apply

• Competitive salary range
• High-impact role supporting core quality systems and compliance initiatives
• Opportunity to collaborate with senior leadership and influence decision-making
• Exposure to diverse QA programs including audits, investigations, and vendor quality
• Dynamic, fast-paced pharmaceutical environment with meaningful work
  
  

What You’ll Be Doing

• Review batch records, SOPs, protocols, and validation documents for compliance
• Lead and support QA/QC projects to ensure timely execution
• Coordinate QA meetings and document key outcomes and action items
• Analyze and present quality metrics for product reviews
• Support deviation investigations, CAPAs, and root cause analysis
• Manage quality systems such as change control, audits, and complaints
  
  

About You

• Bachelor’s degree in a scientific discipline (Chemistry, Biology, or related)
• Strong knowledge of cGMP and pharmaceutical quality systems
• Experience with document review, deviations, and change control
• Proficiency with eQMS and documentation systems
• Excellent communication and organizational skills
  
  

How To Apply

We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to tomt@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19808.