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Technical Writer Jobs

Company

Sterling Engineering

Address Salt Lake City Metropolitan Area, United States
Employment type FULL_TIME
Salary
Category Medical Equipment Manufacturing,Pharmaceutical Manufacturing
Expires 2023-11-06
Posted at 9 months ago
Job Description

We are seeking a talented and detail-oriented Technical Writer to join our team within the medical device industry. As a Technical Writer, you will play a critical role in creating clear and concise documentation for a variety of products, including medical devices, equipment, and related software systems. Your expertise in technical writing and understanding of regulatory requirements will ensure the production of high-quality documentation that meets industry standards.


Responsibilities

  • Work closely with cross-functional teams, including engineers, scientists, regulatory affairs, quality assurance, and marketing, to gather information and ensure accuracy in technical documentation.
  • Review, edit, and proofread technical documentation for accuracy, clarity, and consistency. Ensure that the content aligns with the target audience's needs and is presented in an organized and logical manner.
  • Create and maintain a range of technical documents, including user manuals, standard operating procedures (SOPs), work instructions, product specifications, installation guides, and other relevant technical documentation. Ensure that these documents are accurate, comprehensive, and easy to understand.
  • Stay updated with relevant regulations and standards within the medical device or pharmaceutical industry, such as FDA regulations, ISO standards, and Good Documentation Practices (GDP). Ensure that all documentation complies with these regulatory requirements.


Qualifications

  • Knowledge of medical device or pharmaceutical product development processes is highly desirable.
  • Familiarity with usability testing methodologies and experience conducting user testing on documentation.
  • Proven experience in technical writing within the medical device or pharmaceutical industry
  • Strong understanding of regulatory requirements and industry standards, such as FDA regulations, ISO standards, and GDP.