Demo

Regulatory Specialist

Exactech
Gainesville, FL Full Time
POSTED ON 1/22/2025
AVAILABLE BEFORE 4/21/2025

Regulatory Specialist

Department : Regulatory

Employment Type : Full Time

Location : Gainesville, FL

Reporting To : Sr. Manager, Regulatory Affairs

Description

The purpose of the Regulatory Specialist is to provide services to fulfill the regulatory requirements necessary to achieve global regulatory approvals / clearances and maintain overall regulatory compliance for the company.

Key Responsibilities

  • Preparing and maintaining FDA pre-market submissions, Canadian device license applications and international product registrations for medical devices.
  • Assist in preparing and submitting MDD Class III Design Dossiers for review by the Notified Body.
  • Providing regulatory support for new product development projects :

Design team participation

  • Design Control requirements
  • CE marking requirements / Technical File (STED) / Design Dossier compilation
  • Pre-market regulatory submissions
  • Canadian device license applications
  • International product registrations - STED File organization
  • Product labeling review and approval
  • Ensuring that company procedures, processes and documentation meet the required guidelines for maintaining FDA compliance and ISO / EC / CMDR certification, including the application of Design Control and Risk Management processes.
  • Participate as needed in the complaint handling, corrective and preventive action and internal quality audit processes.
  • Knowing and applying Exactech's Quality Management System and any appropriate federal and international standards.
  • Providing knowledge and support to the company's different business units to enable operation within company and regulatory guidelines.
  • Assisting and supporting other employees, teams, and sales personnel as necessary.
  • Practicing Exactech's Values.
  • Skills Knowledge and Expertise

    Education :

  • Bachelor's Degree from an accredited institution required.
  • Experience :

  • Minimum 2 years experience in FDA / ISO medical devices quality management system standards required
  • 2 years experience in FDA pre-market submissions (510(k) and / or PMA) and international product registrations preferred
  • Functional / Technical Knowledge, Skills and Abilities Required :

  • Technical writing skills required
  • Experience in Design Controls
  • Working knowledge of windows-based office productivity tools including word processor and spreadsheet
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