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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and maintaining technical documentation for regulated medical devices, utilizing tools such as Adobe FrameMaker and structured authoring methodologies. Capable of managing document version control and supporting cross-functional teams to ensure compliance and clarity in documentation.
Highest-signal resume keywords
Technical WritingAdobe FrameMakerStructured AuthoringDocument Version ControlTechnical Documentation Development
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Technical WritingTechnical EditingDocument PublishingXMLContent Management SystemsAdobe AcrobatAdobe PhotoshopHTMLVector Graphics SoftwareRegulated Environment Experience
Soft Skills
MentoringCollaborationAttention to DetailCommunication
Tools & Technologies
Adobe FrameMakerContent Management SystemsDocument Lifecycle Management SystemsTranslation Project Management Tools
Industry Keywords
Medical DevicesTechnical PublicationsRegulatory ComplianceInstructions for UseProduct Lifecycle Management
About the role
Key responsibilities & impact- Develop, update, and maintain IFUs, manuals, quick reference guides, package inserts, technical bulletins, and other product documentation
- Gather technical content from Product Development, Marketing, Regulatory Affairs, and subject matter experts
- Create documentation using Adobe FrameMaker and structured authoring tools for regulated medical devices
- Manage document version control, archival activities, and release processes in Product Lifecycle Management systems
- Coordinate translation projects, including preparation, tracking, review, and finalization of multilingual documentation
- Review and edit documentation for accuracy, clarity, consistency, and compliance
- Support continuous improvement initiatives for documentation processes, workflows, and content management
- Provide documentation guidance to cross-functional stakeholders and mentor less experienced writers as needed
- Develop and maintain Instructions for Use and related product documentation throughout the medical-device product lifecycle
- Support global availability of compliant documentation
Requirements
What you’ll need- Bachelor's degree in Technical Science, English, Journalism, or related writing discipline
- 2+ years of technical writing or technical editing experience
- Experience developing technical documentation in a technical publications or regulated environment
- Advanced experience with Adobe FrameMaker
- Experience with Structured Authoring, XML, and content management systems
- Experience with Adobe Acrobat, Adobe Photoshop, vector graphics software, HTML, and document publishing tools
- For Baccalaureate degrees earned outside of the United States, a degree satisfying 8 C.F.R. § 214.2(h)(4)(iii)(A) is required
- Unrestricted U.S. work authorization required at hire and throughout employment; sponsorship is not offered for roles below Principal level
Benefits
Comp & perks- Health, dental and vision insurance
- Health Savings Account
- Healthcare Flexible Spending Account
- Life insurance
- Long-term disability leave
- Dependent daycare spending account
- Tuition assistance/reimbursement
- Simple Steps global well-being program
- Incentive plans
- 401(k) plan plus employer contribution and match
- Short-term disability
- Paid time off
- Paid holidays
- Employee Stock Purchase Plan
- Employee Assistance Program
- Non-qualified Retirement Plan Supplement
- Capital Accumulation Plan for eligible employees
- Temporary employees: paid sick time as required by applicable state law
- Employee Stock Purchase Plan for temporary employees
- Short-term incentive through the Medtronic Incentive Plan (MIP)