Regulatory Affairs Engineer/Specialist
American Orthodontics
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- Location
- Sheboygan, WI
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 13
- 7 days ago
Career path
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About the company
American Orthodontics
Medical devices · 501 to 1,000 employees
What you'll do
- Support product registrations and regulatory submissions; advise project teams on regulatory requirements.
- Manage regulatory documentation, agency communications, product vigilance, procedures, and audits.
What you need
- A bachelor’s degree in Biomedical Engineering, Biology, Chemistry, Technical Communication, or a similar field is desired.
- Experience with medical devices or other highly regulated products and technical writing is desired; strong communication, thoroughness, and ability to lead multiple activities are expected.
- Education: a bachelor's degree
Key skills
Technical writingLead multiple activitiesAttention to detailWritten and verbal communication
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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