Regulatory Affairs Specialist
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Before you apply
LocationAlpharetta, Georgia, United States
Typefull-time
SeniorityMid
Experience2–3 yrs
DepartmentRegulatory Affairs
Company size1,001–5,000 people
PostedNov 18, 2025 · 11mo ago
Verified live20h ago
May no longer be actively hiring
Posted by the company on Nov 18, 202595% of this company's open roles have been listed for 90+ days
At a glanceSummarised by Seekless from the posting.
Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field
English
2-3 years of regulatory affairs experience within the medical device or IVD industry
Working knowledge of 510(k) submissions and regulatory documentation processes
Solid understanding of FDA regulations and Guidance (510k, PMA, De novo)
Strong organizational and project management skills
Excellent communication, problem-solving, and attention to detail
Ability to work collaboratively in cross-functional teams and manage document workflows
Mandarin
Experience interacting with FDA and other regulatory agencies
Benefits
Health insurance
401(k)
Unlimited PTO
About Us
CorDx, a multi-national biotech organization, focused on pushing the limits of innovation and supply in global health. With over 2000 employees across the world serving millions of users in over 100 countries, 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. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.
Position Summary
The Regulatory Affairs Specialist will support the preparation, review, and submission of regulatory documentation for medical device/IVDs products, ensuring compliance with applicable regulatory requirements including FDA, ISO 13485, and other global standards. This position focus on submitted documents preparing, helping to secure timely product approvals and regulatory clearances.
Key Responsibilities
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Prepare, review, and coordinate the submission of regulatory documents including 510(k), technical files, and other filings to regulatory agencies
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Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards
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Working on analytical performance test with product development teams to draft documentation.
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Perform regulatory assessments for product changes and propose appropriate regulatory pathways
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Maintain documentation and records of all regulatory submissions and correspondence
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Support the preparation for regulatory agency meetings, audits, and inspections
Requirements
Education:
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Bachelor’s degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required
Language:
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English
•
Mandarin Preferred
Professional Experience:
•
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
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.