Ingersoll Randposted 22 days ago
Salt Lake City, UT
Machinery Manufacturing

About the position

The Technical Writer will work under general supervision to develop, create, and/or edit operational, instructional, maintenance, inspection, test procedures and other documentation in support of the development and manufacture of medical devices.

Responsibilities

  • Research and document engineering processes, validation documentation, and specifications.
  • Develop and update process documentation including assembly procedures, test procedures, BOMs, process flows, and process FMEAs.
  • Collaborate openly and effectively with Engineering, Operations, Quality, and Supply Chain, among others, to ensure accuracy and completeness of content.
  • Produce products that conform to the company documentation and Quality Management System (QMS) standards.
  • Recommend formats responsive to technical, operational, quality, and customer requirements.
  • Must possess strong written and verbal communication skills.
  • Ability to multitask and prioritize to meet timelines and milestones.
  • Be highly organized and attentive to details.
  • Maintain design and development documentation to support quality and regulatory process requirements.
  • Support and implement company goals and objectives, policies and procedures, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), FDA QSR and ISO regulations.

Requirements

  • Bachelor's degree in a technical area.
  • Experience in technical communications, writing/ composition, or similar related field.
  • Must be proficient in Microsoft Office Suite.
  • Experience working with cross-functional project teams.
Hard Skills
Technical Documentation
2
Good Manufacturing Practices
1
Medical Device Development
1
Microsoft Office
1
Product Testing
1
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