AIS R&D Technical Communications Intern at Boston Scientific Corporation Malaysia

Arden Hills, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Jan, 26

Salary

0.0

Posted On

07 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Technical Writing, Content Management Systems, XML-Based Authoring, AI-Assisted Writing Tools, Medical Terminology, Documentation Planning, Project Tracking, Attention to Detail, Effective Communication, Collaboration, Content Reuse, User Manuals, Engineering Reports, Product Labels, Regulatory Compliance, Quality Standards

Industry

Medical Equipment Manufacturing

Description

This role follows a hybrid work model, requiring employees to be in our local office at least three days per week. Corporate housing and relocation are available for those who are eligible. Your responsibilities will include: Create and maintain technical documentation including user manuals, product labels, engineering reports, and supporting materials for implantable medical devices. Translate complex engineering and clinical concepts into clear, structured content tailored to diverse audiences across R&D, regulatory, and quality teams. Utilize content management systems (CMS) and desktop publishing tools to organize, version, and publish documentation in compliance with internal standards and regulatory requirements. Apply single-source authoring strategies to streamline content reuse across product families and documentation types. Author and edit structured content using XML-based tools, ensuring consistency, modularity, and compatibility with downstream publishing workflows. Collaborate with engineers and subject matter experts to ensure accurate use of medical terminology and alignment with device-specific language Review and revise documentation for clarity, tone, and adherence to company style guides and quality standards. Support integration of AI-assisted writing tools to enhance efficiency, terminology alignment, and content validation. Contribute to documentation planning and project tracking, ensuring timely delivery of materials for product development milestones and regulatory submissions. Must be a rising senior (grad dates between Fall 2026 - Spring 2027) Pursuing a Bachelors degree in Technical Writing or a writing-related major with technical writing work experience Academic project or work experience with technical writing Must be able to start internship on May 18th or 26th, 2026 and work for 12 weeks Must have reliable transportation to/from work. Experience with single-source authoring tools. Experinece with Content Management Systems (CMS). Experience with XML-based authoring. Experience with AI-assisted writing tools. Has taken a medical termonology course or has medical industry writing experience. Ability to understand and convey complex technical information clearly and concisely. Ability to communicate effectively with diverse, cross-functional teams. Strong written and verbal communication skills. Attention to detail and ability to work independently. Interest in the medical device industry and regulatory environment.

Responsibilities

The intern will create and maintain technical documentation for implantable medical devices, translating complex concepts into clear content for various audiences. They will collaborate with engineers and subject matter experts to ensure accuracy and compliance with internal standards.