About Sequel
Sequel Med Tech is an early-stage company developing the next generation of precision drug delivery devices.
Job Overview
Sequel Med Tech is seeking a CONTRACT Technical Writer to support our rapidly growing software product portfolio. Contract will be 3-6 months with possibility to extend. The successful candidate will utilize their strength as a communicator to serve as a technical translator, distilling engineering and healthcare concepts for a variety of technical and non-technical audiences. Working alongside the Product Managers, the Technical Writer will be responsible for capturing development team activities in the form of requirements, technical documentation, and Quality Management records. If you’ve been looking for a way to combine your technical acumen and liberal arts foundation into a role where you are making a meaningful impact for the world, come join us in defining the future of diabetes management.
Job Responsibilities and Essential Duties
- Responsible for designing, developing, and updating required technical documentation.
- Responsible for technical writing/editing for all types of documentation produced within a modern software development environment.
- Utilize knowledge of word processing software, strong writing and analytical skills to document software capabilities and functionality.
- Document programming standards and procedures. Track and review change control documentation.
- Assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.
- Review current documents- incorporate comments from Manager. Navigate through Veeva (Documentum) system utilizing current templates.
- Notify manager of workflow status and issues.
- Incorporate comments from team members and provide status to manager on review and approval workflow. Follow up with team members on comments.
Minimum Requirements
Education:
Bachelor's degree in a technology or communications field, or equivalent experience
Years of Experience:
1 - 3 Years of experience in technical writing in an FDA-regulated environment
Required Knowledge, Skills and Abilities
- Technical writing abilities and good time management.
- Strong root cause analysis skills with experience regarding quality standards.
- Be able to establish working relationships with other support and production areas in order to gather all the necessary information required.
- Working knowledge of Gitlab, Confluence, Loop, Veeva.
- Proficient in MS Word, Excel, PowerPoint and Outlook.
- Interact well with a diverse group of individuals.
- Self-motivated and willing to be proactive in resolving issues.
- Excellent Verbal and written communication skills.
- Experience collaborating with functional (Quality, Legal, Marketing, etc.) partners to navigate functional gatekeepers.
- Bias towards active collaboration over working in silos and throwing over the wall.
Environmental/Safety/Physical Work Conditions
- Ensures environmental consciousness and safe practices are exhibited in decisions
- Use of computer and telephone equipment and other related office accessories/devices to complete assignments
- May work extended hours during peak business cycles
- Physical requirements such as lifting specific weights
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What We Do
We’re Sequel — a driven team of innovators and problem solvers laser-focused on improving the health and lives of people with diabetes. We’re redefining what diabetes care looks like — so the next chapter is the best.
