Join Encoded Therapeutics as the Director of Quality Assurance in Research Triangle Park and champion quality compliance for clinical manufacturing in gene therapy. Lead all site quality operations to ensure adherence to the highest standards.

As the Site Quality Head, your role is crucial in mentoring a dedicated QA team and navigating the complex landscape of regulatory compliance. Utilize your background in biotech and pharmaceutical quality assurance to influence and direct key quality decisions while ensuring product safety and efficacy. You will be a key player in energetic team collaborations.

Key Responsibilities:
• Drive risk-based quality decision-making processes
• Provide quality oversight of clinical manufacturing operations




• Author regulatory submissions and agency interaction documents
• Lead and support quality team in internal operations
• Manage quality compliance during site inspections

Requirements:
• Bachelor’s or Master’s degree in Life Sciences
• Minimum 12 years in Quality Assurance
• At least 5 years in a leadership position
• Strong understanding of GMP regulations
• Experience in Viral Vector or Gene Therapy products

This position relies on your vast experience to enhance quality assurance processes at Encoded.
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📌 Director of Quality Assurance - Encoded Therapeutics (Newfoundland and Labrador)
🏢 Encoded Therapeutics
📍 Newfoundland and Labrador