Technical Writer Job at PLASTIKON HEALTHCARE, LLC, Lawrence, KS

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  • PLASTIKON HEALTHCARE, LLC
  • Lawrence, KS

Job Description

Plastikon Healthcare is looking for a Technical Writer to review materials, such as SOPs, Specifications, and/or Standard Analytical Method documents, and work instructions for computerized systems. The ideal candidate will be responsible for creating clear and concise documentation that effectively communicates complex information to a variety of audiences. This role requires strong writing, editing, and proofreading skills, along with the ability to conduct thorough research and utilize various software tools.

Responsibilities

  • Collaborate with all departments to obtain an in-depth understanding of products as well as their corresponding documentation requirements.
  • Study drawings, specifications, mock-ups, and product samples to integrate and delineate technology, operating procedure, and detail.
  • Produce high-quality investigations for manufacturing, engineering and laboratory.
  • Product documentation for computerized system job aids, and training documents.
  • Revise existing documentation, ensuring that audiences always have access to accurate information.
  • Provide feedback to product teams to contribute to the continuous improvement of the user experience.
  • Edit, standardize, and make changes to material prepared by others.
  • Interview subject matter experts to plan, develop, organize, write and edit standard operating procedures, processes, policies, user guides, job aids, quick reference cards, data flow. documentation, technical drawings, frequently asked questions and other content.
  • Report on progress of work products and deliverables.
  • Assess, analyze, write, edit and manage end-user training and documentation for technology implementations and updates.
  • Analyze documents to maintain continuity of style of content.
  • Other duties as assigned.

Requirements

  • Bachelor’s degree, five years’ experience.
  • Knowledge of principles and methods for investigation writing and SOP writing with a strong background in pharmaceuticals and/or Medical Device regulations.
  • Proven experience in technical writing or a related field.
  • Strong communication skills with the ability to convey complex information clearly.
  • Proficiency in proofreading and editing technical documents.
  • Familiarity with word processing software and tools such as Microsoft Word and Visio.
  • Ability to conduct thorough research on technical topics.
  • Detail-oriented mindset with excellent organizational skills.

If you are passionate about creating high-quality technical documentation and thrive in a collaborative environment, we encourage you to apply for this exciting opportunity.

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