Stryker is hiring a Senior Technical Writer to join our Technical Publications team supporting the Endoscopy Business Unit. In this role, you will independently lead technical documentation and labeling activities for new product development and sustaining projects. The Senior Technical Writer partners with cross-functional teams to develop compliant, high-quality labeling and technical documentation while driving project execution, process improvement, and labeling strategy. This position serves as a key contributor to divisional objectives by balancing functional expertise, regulatory compliance, and business needs to deliver efficient and effective labeling solutions.
What You Will Do
Lead technical documentation and labeling deliverables for new product development, sustaining, quality, regulatory, and business integration initiatives.
Develop and maintain compliant labeling solutions in accordance with regulatory requirements and quality system procedures.
Manage labeling requirements and content across labeling systems, authoring manuals and technical documentation, and partnering with label designers to ensure accurate and compliant execution of product labels.
Partner with cross-functional teams to define documentation strategies and deliver high-quality labeling solutions that support business objectives.
Drive documentation and labeling activities through all phases of the product lifecycle, balancing quality, compliance, schedule, and business needs.
Perform labeling and documentation assessments to support new product launches, product changes, quality initiatives, and regulatory compliance activities.
Contribute to engineering change requests, product transfers, remediations, NC/CAPA, and continuous improvement initiatives involving technical documentation and labeling.
Utilize content management systems, structured authoring principles, and documentation best practices to improve efficiency, consistency, and scalability.
Identify risks, resolve issues, and proactively drive projects and assignments to successful completion.
What You Will Need
Required
Bachelor’s degree in Technical Writing, Communications, or related field
Minimum of 2+ years of experience in technical writing within the medical device industry
Proficiency in DITA XML authoring and structured content development within content management systems.
Preferred
Experience utilizing technical documentation platforms and product lifecycle management (PLM) tools, such as Arbortext and Windchill
Understanding of translation workflows and global documentation standards for regulatory compliance
Experience working in cross-functional project teams, partnering with subject matter experts (SMEs) to gather, analyze, and incorporate technical requirements and input.
United States of America Pay Ranges:
- USN: $66,500 - $101,800 USD Annual
- US5: $69,800 - $106,900 USD Annual
- US10: $73,200 - $112,000 USD Annual
- US15: $76,500 - $117,100 USD Annual
- US20: $79,800 - $122,200 USD Annual
- US30: $86,500 - $132,300 USD Annual
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.
Skills Required
- Bachelor's degree in Technical Writing, Communications, or a related field
- At least 2 years of technical writing experience within the medical device industry
- Proficiency in DITA XML authoring and structured content development within content management systems
- Experience with technical documentation platforms and product lifecycle management tools such as Arbortext and Windchill
- Understanding of translation workflows and global documentation standards for regulatory compliance
- Experience working in cross-functional project teams and incorporating technical requirements from subject matter experts
Inari Medical Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.
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Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
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Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
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Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.
Inari Medical Insights
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.
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