Boston Scientific Technical Writer - III 

El Salvador, La Libertad, Lourdes 

959458340

Costa Rica-Heredia

Hybrid Roles:

About the role:

Support engineering with the generation, update and maintenance of technical documents.

Responsibilities:

• physician and patient medical device product literature deliverables using Adobe InDesign.
• Manage, organize, and communicate project information and project activitiescross-functionally.
• Represent the Technical Communications function within project core teams.
• Apply corporate and regulatory medical deviceLabeling requirements as it pertains to device product literature.
• Work with other technical communicators to organize Instructions For Use (IFU) and related product literature to support regulatory submissions, market expansion, and product commercialization targets.
• Interface cross-functionally within the product development teams to acquire source material forproduct literature, 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.

Requirements:

• 3+ years of experience working as a technical writer creating procedural-based instruction manuals.
• Demonstrated knowledge of Technical Writing principles and ability to demonstrate such proficiency.

• Demonstrated ability working under the guidance of standard operating procedures.
• Demonstrated ability to understand complex information and explain it in a simplified manner.

Preferred Qualifications:

• Bachelor degree in Scientific and Technical Communications or similar
• Familiarity with the use of Adobe InDesign and ability to demonstrate basic proficiency.
• Advanced degree in a health sciences 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.