Regulatory Affairs Specialist

CorDx is a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2000 employees across the world, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious diseases such as COVID-19, pregnancy, drug abuse, biomarkers, and more. The company is at the cutting edge of technology, artificial intelligence, and data science, aiming to deliver diagnostic solutions to critical healthcare challenges.

About the role

The Regulatory Affairs Specialist will support the preparation, review, and submission of regulatory documentation for medical device/IVD products, ensuring compliance with applicable regulatory requirements including FDA, ISO 13485, and other global standards. This role focuses on preparing submitted documents to secure timely product approvals and regulatory clearances.

Responsibilities

• Prepare, review, and coordinate the submission of regulatory documents including 510(k), technical files, and other filings to regulatory agencies.
• Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards.
• Collaborate with product development teams on analytical performance tests to draft documentation.
• Perform regulatory assessments for product changes and propose appropriate regulatory pathways.
• Maintain documentation and records of all regulatory submissions and correspondence.
• Support the preparation for regulatory agency meetings, audits, and inspections.

Requirements

• Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field.
• 2-3 years of regulatory affairs experience within the medical device or IVD industry.
• Working knowledge of 510(k) submissions and regulatory documentation processes.
• Experience interacting with FDA and other regulatory agencies preferred.
• Proficiency in English; Mandarin preferred.

Skills & Competencies

• Solid understanding of FDA regulations and guidance (510k, PMA, De novo).
• Strong organizational and project management skills with the ability to manage multiple projects and priorities.
• Excellent communication, problem-solving, and attention to detail.
• Ability to work collaboratively in cross-functional teams and manage document workflows.

Benefits

• Comprehensive medical insurance.
• 401(k) plan with company contributions.
• Flexible paid time off (PTO) policy.