Director of QA & Regulatory Affairs

About Us

We are seeking an experienced and highly qualified Director of Quality Assurance and Regulatory Affairs to lead quality systems and ensure compliance with all applicable regulatory requirements. This role will oversee quality assurance processes, regulatory submissions, and audits to maintain product integrity and adherence to industry standards.

Chromo Logic LLC () is a world-class innovation center with advanced scientific research and development in the medical, aerospace and security markets. Covisus Inc. () is a VC-funded spin-off from Chromo Logic that has developed an award-winning and industry-leading technology for tagless tracking of assets based on its vTag® technology.

• Develop and implement quality assurance strategies and regulatory compliance programs (FDA 510(k), PMA, IDE, drug approval, IND, pre-submission)
• Ensure adherence to FDA, ISO, and other relevant standards (IRBs, HRP, clinical study protocols, animal study protocols (IACUC, OLAW, ACURO))
• Oversee internal and external audits, inspections, and certifications
• Manage regulatory submissions and maintain documentation for compliance
• Collaborate with cross-functional teams to ensure quality throughout the product lifecycle
• Lead and mentor QA, regulatory, and safety teams to achieve organizational goals
• Monitor changes in regulations and update company policies accordingly
• Ability to obtain security clearance

• Bachelor’s or Master’s degree in engineering, life sciences, or related field
• 10+ years of experience in QA and regulatory roles
• 5+ years in leadership roles, with a proven track record of managing people and processes
• Excellent communication, leadership, and strategic skills

• Competitive salary and benefits package, including stock options
• Opportunities for professional growth and development
• A collaborative and inclusive work culture
• The chance to work on cutting-edge technology projects that make a real-world impact