Make an impact that reaches healthcare professionals and patients around the world. In this role, you will shape clear, compliant, and user‑friendly instructional content that supports safe and effective use of innovative medical technologies. You’ll join a driven, collaborative team where your expertise directly influences product success, global usability, and regulatory readiness.
This role is remote and can be based in any US location.
What You Will DoDevelop product instructions for use and customer‑facing documentation that is accurate, compliant, and translation‑ready for global users.
Plan, write, and deliver labeling content using technical publishing tools while managing project timelines and deliverables.
Drive labeling activities as an active project team member, ensuring documentation meets medical device regulations and internal quality system requirements.
Coordinate cross‑functional input from engineers, clinicians, and subject matter experts to create technically sound and user‑centered content.
Evaluate and improve documentation quality by interpreting procedures, incorporating labeling standards, and applying topic‑based authoring strategies.
Perform Labeling Specification, Verification, and Global Impact Assessment reviews, applying critical thinking to assess cross‑functional effects of changes.
Manage multiple concurrent projects, escalating issues when needed to maintain compliance and readiness.
Contribute to process improvements, product transfers, and quality system integration efforts, and mentor less experienced writers when appropriate.
Required Qualifications
Bachelor’s degree in Technical Writing, Technical Communications, or related field.
Minimum 2 years of work experience in technical writing or a related discipline.
Preferred Qualifications
Experience working in a regulated industry (minimum 2 years preferred).
Experience with topic based authoring or DITA.
Experience using enterprise content management systems.
Experience with product lifecycle management systems.
Experience with Adobe Creative Suite and Microsoft Office tools.
$66,500 - $132,300 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.Similar Jobs
What We Do
Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.
