Regulatory Affairs Engineer/Specialist

American Orthodontics
  • Sheboygan, WI
    22 days ago

    Job Description

    Duties and Responsibilities

    • Support Engineering and Product Development teams to successfully complete and obtain product registrations

    • Determine the types of regulatory submissions or documentation required for projects with product design changes, manufacturing changes, or labeling changes

    • Advise project teams on subjects such as pre-market regulatory requirements, export and labeling requirements, and/or clinical study requirements

    • Communicate with customers and regulatory agencies to support product registrations

    • Create, manage, and organize technical documentation in a document control system for domestic and international registrations

    • Respond to questions from regulatory agencies and prepare additional documentation as requested

    • Manage projects related to maintaining product registrations in domestic and international markets

    • Support product vigilance activities through review of customer complaints, reportable incident databases, and clinical literature

    • Identify relevant guidance documents, international standards, or consensus standards and ensure these are communicated through corporate policies and procedures

    • Write and/or update Quality Management System procedures, standard operating procedures, and/or work instructions to align with domestic or international laws, guidelines, or standards

    • Maintain current knowledge base of relevant regulations, international standards, and/or guidance documents

    • Participate in internal and external audits

    • Perform additional responsibilities as requested to achieve business objectives

    • This position is 100% in-office in Sheboygan, WI

    Qualifications

    • Bachelor's degree in Biomedical Engineering, Biology, Chemistry, Technical Communication, or similar field from an accredited college or university desired
    • Experience with medical devices or other highly regulated industries/products desired
    • Experience with technical writing desired
    • Demonstrated ability to lead multiple activities simultaneously
    • Demonstrated thoroughness and attention to detail
    • Strong written and verbal communication skills

    Numbers & Facts

    LocationSheboygan, WI

    Skills

    • Biologyunmatched
    • Biomedical Engineeringunmatched
    • Chemistryunmatched
    • Clinical Dataunmatched
    • Clinical Trialunmatched
    • Communication Skillsunmatched
    • Control Systemsunmatched
    • Corporate Communicationsunmatched
    • Corporate Policiesunmatched
    • Detail Orientedunmatched
    • Document Controlunmatched
    • Documentationunmatched
    • Documentation Standardsunmatched
    • External Auditunmatched
    • Internal Auditunmatched
    • International Lawunmatched
    • Leadershipunmatched
    • Manufacturingunmatched
    • Medical Equipmentunmatched
    • Operations Processesunmatched
    • Presentation/Verbal Skillsunmatched
    • Product Designunmatched
    • Product Developmentunmatched
    • Product Supportunmatched
    • Project Designunmatched
    • Project/Program Managementunmatched
    • Quality Managementunmatched
    • Regulationsunmatched
    • Regulatory Requirementsunmatched
    • Regulatory Submissionsunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Systems Maintenanceunmatched
    • Technical Supportunmatched
    • Technical Writingunmatched
    • Writing Skillsunmatched

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