Position Summary

The position of Regulatory Affairs Specialist is responsible for preparing regulatory submissions (IDEs and PMAs) for North America as well as assisting in the implementation of the company's quality goals and objectives. This position will be remote.

Other responsibilities include assisting with compliance activities related to GMP and ISO regulations and associated standards, as well as, assist in the performance of internal quality and regulatory compliance audits.

This role will report directly to the VP of Regulatory Affairs and Quality, North America and will also work closely with the Regulatory Affairs Manager located in the UK.

Listed below are the major responsibilities of the role and a brief description of some of the key tasks to be performed. This list is not totally inclusive, and the person will be expected to complete tasks reasonably requested by the VP of Regulatory Affairs and Quality, North America.

Requirements

Major Responsibilities

Under direction from the Director, Regulatory Affairs, the Sr. Regulatory Affairs Specialist will be responsible for:
• Preparing regulatory submissions (IDE; IDE Supplements; PMA; PMA Supplements, etc.) for submission to the FDA and Health Canada
• Interfacing with the FDA and Health Canada on assigned projects
• Responding to FDA and Health Canada requests for additional information
• Interacting with FDA, Health Canada and/or Notified Body during quality inspections. Responsible for responding to requests for special reports during inspections
• Keeping abreast of changes to US and Canada regulatory requirements and International Standards related to OrganOx products and processes
• Formally communicating regulatory initiatives or changes in the applicable medical device law with company personnel, customers, subcontractors, regulatory agency representatives, and third party organizations
• Reviewing regulatory guidances for assigned projects to ensure compliance with regulations and determining whether regulatory submissions are required
• Prepare visualizations and conclusions for presentation to upper management
• Working with key stakeholders in relation to Regulatory and Quality topic
• This role will require that you work at the Giralda office in Madison NJ for approximately 2 days per week, subject to your manager's direction. This role will require some travel within the US and at times to the UK.

Qualifications
• Working knowledge of FDA processes for medical device compliance
• The ability to write clear regulatory strategies and submissions
• A good understanding of GMP compliance requirements in Quality Control
• Experience in cross-functional collaboration with Manufacturing, Quality, R&D, Clinical and Marketing departments
• Computer proficiency in MS Office (i.e., Word, Excel, PowerPoint)
• Excellent verbal and technical writing skills
• Ability to work independently
• A BS degree in an engineering, life science, or related area
• At least 3 years' regulatory submission experience for Class II/III medical devices

A job description does not imply that the duties stated are the only ones to be performed by the job holder. Job holder will be required to follow any other job-related instruction as reasonably requested by their line manager or their designate.

Benefits

We offer competitive compensation and comprehensive benefits available from day one, including health, dental, vision, disability coverage, and flexible spending accounts. Additionally, we offer a 401(k)-retirement plan with company matching after 90 days, paid time off, holidays, and additional leave benefits, as well as employee discounts and access to our onsite wellness facility. OrganOx supports work-life balance and provides opportunities for ongoing professional development.