Technical Communication Specialist & Labeling Designer - Medical Devices

Regulatory Jobs; Irvine (CA); On-site; USD 68,000 - 102,000; Full time

Benefits offered by this job

Health, Dental and Vision insurance

401(k) plan with employer contribution

Tuition assistance/reimbursement

Job summary

Medtronic seeks a Tech comm Specialist/Writer to develop regulatory labeling and related documentation for Neurovascular products. You will collaborate with product development and cross-functional partners to define labeling strategy and release plans while ensuring compliance with US/EU regulations.

The role requires 2+ years in regulatory labeling or technical writing for medical devices, proficiency in InDesign, CMS, and translation management, and occasional domestic/international travel.

Qualifications

• Requires a Baccalaureate degree.
• Minimum of 2 years of regulatory/product compliance, labeling, technical writing, or technical editing experience in the medical devices industry.
• Advanced experience with structured authoring using XML and CMS; proficiency with Adobe Acrobat and Photoshop; HTML experience; experience writing for a global audience.

Responsibilities

• Develop regulatory tech comm and labeling strategy; create plans to support document release activities.
• Identify IFU/labeling requirements and obtain content information from various sources.
• Learn and understand the design and behavior of the company’s products.
• Design, develop, and maintain IFU/labeling using Adobe InDesign; control versions and archives.
• Identify translation requirements and manage translation projects to completion.
• Manage change control and administrative documentation in the PLM system.
• Apply US/EU regulations and guidance (21 CFR, EU MDR, ISO standards) and related quality systems.
• Perform quality checks and proofreading of artworks; complete projects independently.

Skills

Regulatory knowledge

Technical writing

Technical editing

Labeling compliance

Education

Baccalaureate degree

Tools

Adobe InDesign

Adobe Acrobat

Photoshop

HTML

CMS

XML

Job description

We anticipate the application window for this opening will close on - 24 Oct 2026

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

Across our global Neuroscience organization, we advance care for some of medicine’s most complex neurological and spinal conditions. By combining innovative technology, data-driven insights, and deep clinical expertise, we partner with physicians and health systems to improve how patients are treated and supported throughout their care journey.

Our Neurovascular operating unit advances treatment of stroke, brain aneurysms, and vascular disorders through innovative endovascular technologies. With devices designed for revascularization, embolization, and precise intervention, we support clinicians in deliveringtimely, effective care for complex neurovascular conditions.

Check us out on LinkedIn: Medtronic Neurovascular

Responsible for developing, maintaining, and releasing labeling and technical documentation for Neurovascular products, including all preprinted labeling, Instructions for Use, user guides, system manuals, quick reference guides, package inserts, label stocks, and other related technical literature. Collaborates with product development and cross-functional partners to define labeling strategy, gather labeling requirements, communicate complex information clearly, create plans to support document release activities, and coordinate translation projects.

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross‑functional collaboration as we work together to engineer the extraordinary.

Responsibilities may include the following and other duties may be assigned.

• The Tech comm Specialist/ Writer responsible for developing regulatory tech comm and labeling strategy. Create plans to support document release activities from start to end.
• Identify IFU/labeling requirements and obtain necessary content information from various sources.
• Learn and understand the design and behavior of the company’s products.
• Design, develop, and maintain IFU/labeling using Adobe InDesign and other software applications. Control IFU/labeling versioning and maintain the IFU archives.
• Identify IFU/labeling translation requirements, prepare and manage translation projects to completion.
• Manage change control and perform the administrative documentation tasks required to establish and track IFU/labeling in a Product Lifecycle Management system.
• Understands and applies relevant US and EU regulations, standards, and guidance documents (e.g., 21 CFR, EU MDR, IMDRF, ISO20417, ISO15223, and ISO 10555), as well as Medical Device Quality Systems (e.g., ISO 13485) and Risk tools (e.g., ISO 14971)
• Continuously evaluate business processes, identify improvement opportunities, and implement improvements.
• Perform quality checks and proofread the artworks.
• The Tech comm Specialist/ Writer is expected to complete projects independently, manage their own priorities, apply company procedures to resolve issues, identify and pursue improvement projects, and may be required to manage the user documentation pool for a specific business segment or segments.
• The Tech comm Specialist/ Writer is expected to manage within a matrixed environment, where direction, prioritization of work, and other daily activities may be established via an indirect reporting relationship.
• Occasional domestic and international travel may be required.
• All activities must be performed in compliance with the Quality System.
• Performs duties in compliance with environmental, health, and safety‑related site rules and policies.
• All other duties as assigned.
• Travel requirement: Less than 10%

Required Knowledge and Experience:

• Requires a Baccalaureate degree
• Minimum of 2 years of regulatory/product compliance, labeling, technical writing, or technical editing experience in the medical devices industry.

Nice to Have:

• Advanced experience with Structured Authoring using XML and content management solutions(CMS).
• Advanced Experience with Adobe Acrobat® and PhotoShop® software, vector graphics software (e.g. Adobe Illustrator®) and HTML.
• Experience writing for a global audience.
• Experience with CMS

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

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.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

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):$68,000.00 - $102,000.00This 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 applies solely to candidates hired within the United States (local-market compensation and benefits will apply to others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, andSimple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees: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 (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

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.

If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.