Job Details

Regulatory Affairs Manager - IVD and 510K

Regulatory Affairs Manager - IVD and 510K

15 hours ago Be among the first 25 applicants

This range is provided by CorDx. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$90,000.00/yr - $150,000.00/yr

Who is CorDx?

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 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 disease such as COVID-19, pregnancy, drugs of 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.

Job Description

We are seeking a highly motivated and experienced Regulatory Specialist to join our Regulatory Affairs team. The ideal candidate will have a strong background in IVD (In Vitro Diagnostics) and experience with 510(k) preparation and submissions to ensure compliance with FDA and other regulatory body requirements.

Responsibilities

· Prepare and submit 510(k) applications for IVD products to ensure timely market entry.

· Manage all aspects of regulatory submission processes, including documentation, timelines, and communication with regulatory bodies, as needed.

· Conduct regulatory risk assessments and develop mitigation strategies for IVD products.

· Stay updated with regulatory changes and ensure all IVD products comply with current regulations.

· Liaise with internal departments (R&D, Quality, Manufacturing) to gather necessary documentation and data for regulatory submissions.

· Provide regulatory guidance on product development projects to ensure compliance from concept to commercialization.

· Review and provide input on product labeling, promotional materials, and change controls to ensure regulatory compliance.

· Assist in the development and implementation of regulatory strategies and update stakeholders on regulatory developments affecting the company's products.

Requirements

• Bachelor's degree in Life Sciences, Biotechnology, Regulatory Affairs, or a related field.
• Minimum of 5 years of experience in relevant industry with min or 3 year hands on experience in 510(k) preparations and submissions.
• Strong understanding of FDA regulations, guidance documents, and processes related to IVD products.
• 10 year work experience;
• More than 5 years team management experience;
• Manage team subordinates more than 5;
• The average job tenure is 30 months;
• Life Science industry,IVD prefer;
• Less 7 companies, no consulting
• Extensive knowledge of FDA regulations, ISO 13485, and other relevant standards.
• Certification in quality management (e.g.,RAC ASQ CQE, CQA) is a plus.
• Experience in medical device IVD Quality Assurance is a plus.
• Health Care Plan (Medical)
• 401K
• Paid Time Off and Paid Sick Leave
• Training & Development

We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Management

Referrals increase your chances of interviewing at CorDx by 2x

Inferred from the description for this job

Medical insurance

401(k)

Get notified about new Regulatory Affairs Manager jobs in San Diego, CA

Program Administrator (Healthcare referral capture) - Fully Remote

Director of Regulatory Affairs AND Manager/Sr. Manager of RA(In Vitro Diagnostics Experience Required)

Security Officer - Third Shift (Night Shift)

San Diego Metropolitan Area $130,000.00-$190,000.00 5 days ago

Staff Specialist Regulatory Affairs (Hybrid)

FBI Special Agent: JD/Law/Legal Expertise

Senior Legal Assistant (Civil Litigation Option)

Director, Pharmacovigilance Safety Operations

Quality Assurance Manager, Calibration Laboratory (Depot)

Multiple Positions at Mitchell International, Inc

Contract Specialist - Managed Care Payor Contracting

We're unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

J-18808-Ljbffr