Shape the future of quality assurance at Encoded Therapeutics as the Site Quality Head in Research Triangle Park. Your vision for CGMP compliance and risk management will ensure the safety and efficacy of gene therapies. This role involves leading all Site Quality Operations, from mentoring QA teams to ensuring compliance with regulatory standards.

Leverage your extensive knowledge in biotechnology to drive operational strategies that align with global regulatory expectations, oversee critical quality metrics, and maintain documentation integrity. Help pave the way for cutting-edge solutions in the treatment of genetic disorders. Key Responsibilities:
Lead Site Quality Operations and CGMP compliance
Manage and mentor a dedicated QA team




Author and review relevant regulatory documentation
Provide oversight for clinical manufacturing and supply chain quality
Support and conduct regulatory body inspections Requirements:
Minimum of 12 years in Quality Assurance within biotech
5+ years in senior management roles
Solid background in Gene Therapy, AAV preferred
Solid knowledge of regulatory guidelines (21 CFR, USP)
Bachelor’s or Master’s degree in Life Sciences Elevate quality and compliance standards in gene therapy at Encoded Therapeutics!

📌 Site Quality Head At Encoded Therapeutics Morrisville
🏢 Encoded Therapeutics
📍 Morrisville