Technical Writer (Pharma//Med Devices) (20-00098) – AZ – Tucson

The primary responsibility of this position is to act as the Technical Writer on project teams, attend meetings, maintain project schedule and update the Supervisor of the Technical Documentation Department. Involved in the creation, review, revision and approval and publication of documentation and labeling for all products. Assists in the coordination and maintenance of corporate standards and certificate library management activities.
Facilitates project activities and internal customer support.  
Provides guidance and direction to technical teams as needed.  
Serves as a primary interface between project teams and Technical Documentation Department, acts as liaison to project leader, conducts formal meetings, track project status and resolves any communication barriers.  
Facilitates the timely development, change, review and approval of documentation according to project schedules, including the resolution of resource issues relative
to processing of such documentation.
Designs, develops, tests, and maintains documentation for products associated with the design, manufacture, test, release, installation, and distribution within established -schedule and budget targets.  
Creates, writes and edits high quality text and graphics, using easy-to-understand grammar, excellent writing structure and good punctuation.  
Uses desktop publishing tools skillfully to produce efficient and accurate documentation.  
Communicates affectively with interdepartmental teams and external vendors/customers.  
Assists in ancillary services and interdepartmental activities or applications required for publication, preparation, storage and delivery of documentation.  


  Bachelor's Degree in a scientific discipline or business administration or other related technical field.


  5 years direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry.
  Authoritative knowledge of current US and International regulations as it pertains to documentation (e.g., FDA, ISO, IVDD and 21 CFR 11), and control of electronic records.
  Demonstrable record of working on project teams while working on multiple projects.
  Experience with international regulatory requirements preferred.

Source: Job Diva – Job Listing

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