As the Technical Publications Specialist, you will play a key role in ensuring our medical device labeling is clear, compliant, and accessible, supporting safe and effective use across global markets. You'll collaborate with cross-functional teams and external partners to deliver high-quality documentation that meets global regulatory standards and enhances patient safety. This is a hybrid position. You will need to live within commuting distance to our Weston, Florida or Mahwah, New Jersey offices. You will be expected to work onsite 2 days per week and may work remotely on the remaining days.
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Job Type
Full-time
Career Level
Entry Level
Industry
Miscellaneous Manufacturing
Education Level
Bachelor's degree
Number of Employees
5,001-10,000 employees