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
Location
Sheboygan, 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
Knowledge Baseunmatched
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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