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REGULATORY DOCUMENT QUALITY ASSURANCE CONSULTANT
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REGULATORY DOCUMENT QUALITY ASSURANCE CONSULTANT

Job Description

REGULATORY DOCUMENT QUALITY ASSURANCE CONSULTANT, Mahwah, NJ
6+ Month Contract

Responsibilities:
  • Researches, prepares and edits complex technical documents.
  • Ensures documents meet editorial and customer specifications and adhere to standards for quality, graphics, format, and style.
  • Interfaces with writers, illustrators, word processors, and subject matter experts in coordinating and preparing the edited draft.
  • Participates in the publishing of formatted documentation in various media.
  • Maintains current knowledge of relevant technical subject matter as assigned.
  • Participates as member of project team.
  • Tracks project documentation through creation, approval, publication, and update lifecycle.


Job Requirements

Experience:
  • Must have Manufacturing background or knowledge.
  • Preferred Medical Device or Pharma environment
  • Electronic Management System Knowledge (Windchill)

Job Snapshot

Employment Type Contractor
Job Type Pharmaceutical, Consultant, Manufacturing
Education 4 Year Degree
Experience Not Specified
Manages Others No
Industry Pharmaceutical
Required Travel Not Specified
Job ID EB14-00229
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REGULATORY DOCUMENT QUALITY ASSURANCE CONSULTANT


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