Technical Writer 76 views2 applications
- Salary Offer As per standards
- Total Years Experience 5+ years of experience in particular field
- Dress Code Casual
- Working Hours REMOTE JOB 8 hours
Candidates with exposure in GE/ Siemens/ Philips/ Storz/ Carl Zeiss/ Skanray/ Stryker… with 5+ years’ experience are welcome!
RESPONSIBILITIES & DUTIES
Content Creation and Editing
For new products and software, responsible for production of full set of technical
documents, including IFUs, QRGs, Specifications Sheets and Service Manuals.
For all existing products and software in the KUBTEC portfolio, responsible for managing
requested edits and proactively ensuring all technical documents are kept up-to-date.
Coordinates and administers language translations of technical documents and other
product collateral as needed.
Directly updates documents, including minor design changes. Partners with Graphic Design
team only when extensive design or layout changes required.
Gathers key technical input from cross-functional experts, such as engineers, product
managers, service and quality assurance.
Endeavors to understand the target audience to tailor documentation to their knowledge
level and needs.
Maintains a technical document list showing current revision levels for product
Maintains a list of technical documents in development or under revision, with anticipated
completion dates. Communicates dates to cross-functional leaders.
Leads the cross-functional review and approval process, ensuring timely inputs from all
stakeholders, and overall on-time delivery of documentation.
Presents new innovative approaches to improve technical writing process to best perform
the tasks of the department and serve the needs of the company.
EDUCATION AND EXPERIENCE
Bachelor’s degree required, ideally in technical/scientific subject. Advanced degree (Master’s,
10+ years or more work experience. At least 5 years of experience working on technical
documents, preferably in the medical device / medtech industry.
Familiarity with regulatory requirements, such as FDA guidelines for medical device
Excellent organizational and project management skills; ability to work both independently and
in a team, managing multiple tasks and deadlines.
Excellent written and verbal communication skills.
Detail-oriented with a focus on accuracy and precision.
Ability to anticipate and proactively address potential issues and ask the right questions.
A team player with a positive attitude and great ability to build and maintain relationships.
Willing to personally roll up sleeves and get the job done. Self-motivated with strong work ethic.
Proficiency in using documentation tools and software (e.g., Microsoft Office Suite, Adobe
Familiarity with InDesign and AutoCAD drawing software.
Knowledge of human factors principles for optimized IFU design a plus.