Boston Scientific Sr Technical Writer HEREDIA 

Costa Rica, Heredia 

649925427

Costa Rica-Heredia

Hybrid Roles:

About the role

Maintain and ensure document integrity, readability and consistency, and provide information and challenge current systems to best utilize document/written communication technologies.

Your responsibilities include:

• Author physician and patient medical device product literature deliverables using Adobe InDesign.

• Manage, organize, and communicate project information and project activities cross-functionally.

• Represent the Technical Communications function within project core teams.

• Apply corporate and regulatory medical device Labeling requirements as it pertains to device product literature.

• Work with other technical communicators to organizing Instructions For Use (IFU) and related product literature for to support regulatory submissions, market expansion, and product commercialization targets.

• Interface cross-functionally within the product development teams to acquire source material for documents and to develop an understanding of BSC Neuromodulation device hardware and software products.

• Interface with, and participate in the management of, third party translation suppliers to ensure that global product literature content is translated accurate per schedule.

Required Qualifications:

• University bachelor’s degree in Scientific and Technical Communications or similar

• 5+ years of experience working as a technical communicator creating product labeling literature (IFUs) within the medical device or pharmaceutical industry.
• Proficient in the use of Adobe InDesign and ability to demonstrate such proficiency.
• Demonstrated knowledge of Technical Writing principles and ability to demonstrate such proficiency.

• Demonstrated ability working under the guidance of standard operating procedures governing the development of medical device product labeling.
• Please submit Resume in English

Preferred Qualifications

• Advanced degree in a health science or a scientific field of study
• Demonstrated knowledge of the FDA code of federal regulations 21CFR parts 820 and 801, as well as the EU MDR regulations governing medical device labeling.
• Experience working with medical device labeling translation suppliers, including authoring content for translatability.