Agenus

Technical Writer (Temp)

US-MA-Lexington
Job ID
2017-1273
Category
Research

Overview

We are looking for Candidates to assist with writing Batch Records and SOPs for a biopharmaceutical manufacturing facility.

Responsibilities

  • Paper batch record authoring/revision/template creation
  • CAPA execution/follow-up for document revisions
  • SOP revisions/authoring
  • Update/create training documents w/ training specialist

Qualifications

Skills:

  • Strong technical writing skills
  • Experience authoring and revising cGMP documentation for commercial operations
  • Advanced proficiency in MS word
  • Working knowledge of cGMP document control systems
  • Intermediate knowledge of biopharmaceutical operations preferred
  • Excellent verbal and writing communication skills 
  • Ability to handle multiple tasks independently and manage competing priorities 
  • Excellent collaboration skills with focus on timely delivery 

 

Education:

  • Bachelors degree in a Scientific discipline
  • Technical writing certification preferred
  • >2 years relevant experience in the pharmaceutical, biotech, medical device, or other regulated environment

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