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Regulatory Affairs Engineer/Specialist

United StatesUnited States·Sheboyganmid
Legal & ComplianceRegulatory
3 views0 saves0 applied

Quick Summary

Technical Tools
Legal & ComplianceRegulatory

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

Location & Eligibility

Where is the job
Sheboygan, United States
On-site at the office
Who can apply
US

About this job

Who can apply
United States
Posted
20 days ago
Employer
has 8 open jobs on Jobera.

Listing Details

Posted
October 13, 2026
First seen
October 13, 2026
Last seen
November 2, 2026

Posting Health

Days active
19
Repost count
1
Trust Level
18%
Scored at
November 2, 2026

Signal breakdown

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Regulatory Affairs Engineer/Specialist