What are the responsibilities and job description for the Technical Writer position at AltimateMedical?
Brief Description
We are seeking a skilled and detail-oriented Technical Writer to join our team in the Durable Medical Equipment (DME) and Patient Positioning Industries. As a Technical Writer, you will be responsible for creating, editing, and maintaining a wide range of technical documentation for our medical devices and equipment. You will work closely with engineers, product managers, and regulatory specialists to ensure that documentation complies with industry standards and provides clear, accurate, and user-friendly information.
Essential Functions
Collaboration & Coordination: Regulatory Compliance: Quality Assurance & Testing: Continuous Improvement:
EDUCATION AND/OR EXPERIENCE
Beyond pay, our market-leading benefits are designed to support your wellbeing. These include medical, dental, vision, and life insurance, as well as short- and long-term disability coverage. We also provide a health savings account with company match, a retirement plan with employer contributions through Vanguard, and access to the Granite Assistance Fund for support when it’s needed most. We value time for rest and personal growth, offering generous paid time off, including volunteer time off and paid holidays.
We are seeking a skilled and detail-oriented Technical Writer to join our team in the Durable Medical Equipment (DME) and Patient Positioning Industries. As a Technical Writer, you will be responsible for creating, editing, and maintaining a wide range of technical documentation for our medical devices and equipment. You will work closely with engineers, product managers, and regulatory specialists to ensure that documentation complies with industry standards and provides clear, accurate, and user-friendly information.
Essential Functions
- Document Creation & Maintenance:
- Develop, write, and maintain user manuals, installation guides, operation instructions, and maintenance procedures for products.
- Create and update product documentation such as Design History Files (DHF) to ensure accuracy, clarity, and compliance with regulatory requirements (e.g., ISO, FDA).
- Write standard operating procedures (SOPs), work instructions, and training materials for internal teams and end-users.
- Collaborate with product development, engineering, and regulatory teams to gather technical information and ensure correct and consistent product details.
- Review and edit technical content from subject matter experts to ensure clarity and alignment with brand and regulatory guidelines.
- Work with the marketing, engineering, and quality teams to integrate relevant compliance language and product features into the documentation.
- Ensure all documentation adheres to relevant industry regulations (e.g., 21 CFR Part 820, ISO 13485, IEC 60601).
- Review and proofread technical documents for accuracy, grammar, and consistency.
- Assist with Verification and Validation Testing and work closely with the product team to ensure the documentation complies with regulatory standards.
- Stay updated on industry trends, regulatory changes, and advancements in medical equipment to continuously improve documentation practices.
- Provide feedback and recommendations for improving product manuals and documentation processes.
- General Requirements:
- Follows safety procedures and maintains a clean and safe work environment.
- Utilizes appropriate personal protective equipment where/when necessary.
- Contributes to a respectful, non-hostile, non-violent work environment.
- Understands the purpose, value, and impact work has on product customers and users.
- Other duties as assigned.
EDUCATION AND/OR EXPERIENCE
- Bachelor's degree in Technical Writing, Communications, Engineering, or a related field preferred.
- 3 years of experience in technical writing, ideally in the medical device, healthcare, or DME industry.
- Familiarity and ability to understand medical device regulations, including FDA requirements and ISO 13485 standards.
- Strong writing, editing, and proofreading skills with a keen eye for detail.
- Ability to translate complex technical concepts into clear, user-friendly language.
- Mechanical aptitude to be able to simply explain functionality of products and mechanisms.
- Experience working with content management systems (CMS), documentation tools and version control systems (e.g., GrandAvenue, MS Word, MS Excel).
- Strong organizational skills and the ability to manage multiple documentation projects simultaneously.
- Excellent communication and interpersonal skills for collaborating with cross-functional teams.
- Lift up to 25 pounds.
- Ability to work in an office environment or remotely.
- Travel to manufacturing or product testing sites as needed (up to 25% of the time).
Beyond pay, our market-leading benefits are designed to support your wellbeing. These include medical, dental, vision, and life insurance, as well as short- and long-term disability coverage. We also provide a health savings account with company match, a retirement plan with employer contributions through Vanguard, and access to the Granite Assistance Fund for support when it’s needed most. We value time for rest and personal growth, offering generous paid time off, including volunteer time off and paid holidays.