Exactech
Regulatory Specialist
Exactech, Gainesville, Florida, us, 32635
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 ResponsibilitiesPreparing 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 participationDesign Control requirementsCE marking requirements / Technical File (STED) / Design Dossier compilationPre-market regulatory submissionsCanadian device license applicationsInternational product registrations - STED File organizationProduct 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 required2 years experience in FDA pre-market submissions (510(k) and/or PMA) and international product registrations preferredFunctional/Technical Knowledge, Skills and Abilities Required:
Technical writing skills requiredExperience in Design ControlsWorking knowledge of windows-based office productivity tools including word processor and spreadsheet
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 ResponsibilitiesPreparing 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 participationDesign Control requirementsCE marking requirements / Technical File (STED) / Design Dossier compilationPre-market regulatory submissionsCanadian device license applicationsInternational product registrations - STED File organizationProduct 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 required2 years experience in FDA pre-market submissions (510(k) and/or PMA) and international product registrations preferredFunctional/Technical Knowledge, Skills and Abilities Required:
Technical writing skills requiredExperience in Design ControlsWorking knowledge of windows-based office productivity tools including word processor and spreadsheet