Lab Supervisor at Symphony Spine and Pain – Ormond Beach, Florida

The Lab QA Supervisor oversees quality assurance operations within a toxicology laboratory, ensuring compliance with regulatory standards, accuracy of test results, and continuous improvement of laboratory processes. This role supports both scientific integrity and regulatory readiness.

1. Quality Assurance Oversight

• Develop, implement, and maintain QA programs for toxicology testing.
• Ensure compliance with standards such as GLP (Good Laboratory Practice), CLIA, CAP, and FDA regulations.
• Monitor laboratory processes to ensure data integrity and reliability.

2. Audits & Compliance

• Conduct internal audits and inspections.
• Prepare for external audits by regulatory agencies and accrediting bodies.
• Investigate deviations, non-conformances, and implement corrective/preventive actions (CAPA).

3. Documentation & Reporting

• Review and approve SOPs (Standard Operating Procedures), protocols, and reports.
• Maintain QA records, audit trails, and validation documentation.
• Ensure proper documentation of toxicology test results and procedures.

4. Method Validation & Data Review

• Oversee validation and verification of toxicology testing methods (e.g., drug screening, LC-MS/MS).
• Review analytical data for accuracy, precision, and compliance.

5. Staff Supervision & Training

• Supervise QA staff and support laboratory personnel on QA practices.
• Conduct training on quality systems, regulatory requirements, and documentation standards.
• Evaluate staff performance related to QA compliance.

6. Continuous Improvement

• Identify areas for process improvement and implement quality initiatives.
• Track quality metrics (e.g., error rates, turnaround times).
• Promote a culture of quality and regulatory compliance.

Education

• Bachelor’s or Master’s degree in Chemistry, Biology, Toxicology, or related field.

Experience

• 3–7+ years in a toxicology or clinical laboratory.
• Experience in QA/QC and regulatory compliance.

Skills

• Strong knowledge of GLP, CLIA, CAP, and FDA guidelines.
• Experience with toxicology instrumentation (e.g., GC-MS, LC-MS/MS).
• Excellent analytical, organizational, and leadership skills.
• Attention to detail and problem-solving ability.

• Laboratory setting with exposure to biological samples and chemicals.
• May require occasional extended hours during audits or investigations.

• Leadership and team management
• Regulatory expertise
• Critical thinking
• Communication and documentation
• Ethical judgment and integrity