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
| Location | Sheboygan, WI |
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