Senior Technical Writer

🔥 0 minutes ago

🏄 California, Michigan, +1 more states – Remote

🏄 California – Remote 🚗 Michigan – Remote 🤠 Texas – Remote

💵 $66.5k - $132.3k / year

⏰ Full Time

🟠 Senior

🔏 Technical Writer

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Stryker

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1941

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Stryker is a global leader in medical technology, providing innovative products and services across the healthcare sector. With a presence in countries across the Americas, Asia Pacific, Europe, and the Middle East & Africa, Stryker offers a wide range of medical technologies, including orthopedic implants, surgical equipment, and advanced hospital devices. The company is committed to improving patient outcomes and healthcare efficiency. Stryker continues to expand its global reach, offering localized solutions to meet diverse healthcare needs worldwide.

📋 Description

• 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 • Author manuals and technical documentation and partner with label designers to ensure accurate and compliant product labels • Partner with cross-functional teams to define documentation strategies and deliver high-quality labeling solutions • Drive documentation and labeling activities through all phases of the product lifecycle • Perform labeling and documentation assessments for 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 • Utilize content management systems, structured authoring principles, and documentation best practices • Identify risks, resolve issues, and drive projects and assignments to completion

🎯 Requirements

• 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 • 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

🏖️ Benefits

• Remote or hybrid or onsite work flexibility • 10% travel percentage • Equal opportunity employment