Step into a leadership role as the Site Quality Head at Encoded Therapeutics in Research Triangle Park. Oversee quality assurance operations to ensure compliance with CGMP standards and regulatory guidelines.

As the Associate Director/Director, you'll drive quality excellence within the clinical manufacturing setting, focusing on risk assessment, documentation integrity, and continuous improvement initiatives. Your expertise in gene therapy and robust quality assurance will guide compliance efforts that profoundly affect patient safety and product reliability.

Key Responsibilities:
• Maintain current GMP regulatory knowledge
• Mentor QA personnel and lead performance improvement
• Provide operational oversight for batch disposition




• Review production documentation for compliance
• Conduct root-cause analysis for quality incidents

Requirements:
• Education in Life Sciences; Bachelor’s or Master’s
• At least 12 years in Quality Assurance
• 5 years in a senior management role
• Comprehensive understanding of 21 CFR and ICH regulatory requirements
• Experience in Advanced Therapy Medicinal Products

Bring your leadership skills to advance quality assurance in the biotech sector at Encoded Therapeutics.
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📌 Site Quality Head - Encoded Therapeutics (Newfoundland and Labrador)
🏢 Encoded Therapeutics
📍 Newfoundland and Labrador