Technical Writer

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  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
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Technical Writer

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    Technical Writer
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DAVIS Companies has partnered with a leader in Biomedical manufacturing to identify a Technical Writer to join their team! Local candidates to Miami area only please. 

Responsibilities of the Technical Writer:

  •  Develops technical training programs and support materials for chemistry and immunoassay automation
  • Utilize principles of instructional design in course development projects
  • Apply different adult learning styles and modalities to e-Learning instruction
  • Compliance with all safety, quality and regulatory requirements such as: ISO, GMP and FDA
  • Deliver training to internal employees and customers for set up, operation, calibration, quality control, maintenance, and troubleshooting

Course Curriculum Development

  • Use development content tools (Articulate, Camtasia, Storyline) to create effective and engaging e-learning
  • Analyze and synthesize information from multiple sources to prepare a variety of e-learning training content
  • Design and develop training materials including: storyboards, participant and instructor guides. All materials will be based on content and specifications provided by subject matter experts.
  • Recommend appropriate and innovative solutions, and complete the design and development of all web-based, virtual, on-the-job and classroom materials.
  • Build a plan into each learning project for evaluating the successful achievement of training outcomes.


  • 2+  Years in Medical Device, Chemistry or Immunoassay technical writing experience
  • 5+ years experience developing technical training programs for medical device companies (work or school experience would apply in total years)
  • Bachelor's degree in Clinical Laboratory Science, Biomedical Engineering or related field with 2+ years of experience OR Master’s degree in field with 0-2 years of experience
  • Previous experience in the Biotechnology/Life Sciences industry or in a Clinical laboratory is preferred 




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