Technical Writer



The goal for this role is to develop and improve biotechnology technical documentation.


Job duties:

  • Revises existing or develops new policies, SOPs, WIs in support of the business process to ensure compliance with applicable regulatory requirements (GxP, HIPAA, HITECH, HITRUST, etc.)
  • Research, evaluate, and recommend tools and methods to improve documentation development efforts
  • Research and document new and emerging biological technologies
  • Ensures quality control of all documents, maintaining continuity of style and content



  • B.S. or M.S. in biological science, clinical laboratory science, medical technology, technical writing or other relevant field
  • 5+ years of technical documentation experience preferably in a regulated biotechnology/healthcare environment
  • Ability to translate complex technical information into easily understandable documentation
  • Must have excellent English grammar, spelling, punctuation, and sentence structure abilities in order to write clear and accurate documents
  • Excellent attention to detail, strong organization skills, plus ability to prioritize and multi-task
  • Proficiency in Microsoft Office, Word, Excel and PowerPoint
  • Prior experience in oncology specific sample sourcing and/or academic collaborations highly preferred


The company offers:

  • Part time job (10 hours a week) primarily remotely¬†
  • Opportunity to join the fast growing business of biotechnology


Qualified candidates interested in this position should send their resume via email to Natalia Sobetska-Koloda, HR Generalist ([email protected])