At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Careers That Change Lives

As a Technical Writer, you will support the production of customer facing product documentation, including but not limited to : user's guides, service manuals, and instructions for use (IFUs). This includes labeling for both clinicians and patients that accompany medical device products that conform to the Medtronic documentation and quality assurance standards . Projects include R&D new product development as well as sustaining activities/legacy document maintenance f o r various products produced by the Medtronic Neuroscience portfolio . You will c o llect inputs from cross-functional technical staff to gather data for documentation , as well as r esearch and translate technical information into manu als and/or web-based documents for nontechnical and technical users. Responsible for s upporting documentation to the customer-facing literature which may include labeling design plans, trace documents , technical reviews and verification deliverables. You will support product documentation updates to comply with EUMDR , FDA and other regulatory body requirements by incorporating customer inputs and ensur ing standardization of document development to comply with Medtronic d esign standards.

A Day in the Life

• Manage all aspects of document development and assist in production release , including draft reviews and formal label ing approvals, coordination of translations, and initiating CO /CA release.

• Revise, edit, and format legacy product documentation as required, including but not limited to user's guides, service manuals, instructions for providers (IFPs), and instructions for use (IFUs).

• Ensure compliance of labeling with all applicable regulatory/QSR requirements.

• Create, edit, and format documentation as part of the compliance with requirements from the European Union (EU Medical Device Regulation) .

• Deliver supporting documentation to the labeling product, including labeling design plans, trace documents, technical reviews and verification deliverables.

• Effectively manage multiple projects, changes in project scope, and shifting priorities to maintain project requirements and ensure deadlines are met.

• Collaborate with departmental and cross-functional peers to ensure proper resolution to questions and issues during the document development process.

• Continually review the document development process to ensure quality in labeling output.

Must Have: Minimum Requirements

To be considered for this role, please ensure the minimum requirements are evident on your resume.

• Bachel o r ' s degree required and 2 years of technical writing experience

or

• A dvanced degree with 0 years of technical writing experience

Nice to Have

• Advanced writing/editing skills

• Self-directed and highly organized

• Ability to manage multiple priorities

• Excellent communication skills

• Cross-functional collaborative nature

• Product Lifecycle Management software experience

• Working in a federally regulated environment (FDA)

• European Union Medical Device Regulation (EUMDR)

• Medical terminology experience

• Familiar with the p rincipals of neuromodulation

• Product development w orkflow

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD):$71,200.00 - $106,800.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

Medtronic benefits and compensation plans

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 90,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here .

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

At Medtronic, most positions are posted on our career site for 3-7 days.