The Opportunity

We are looking for a QA Document Coordinator, working in the Pharmaceuticals & Medical Products industry in Cambridge, Massachusetts, United States.

Job description:
  • Maintains metrics for periodic review.
  • Makes updates in Veeva based on doc owner response
  • Communicates with and assist end users understanding process and holding accountable to committed target dates.
Details

The pay range we are offering is 35 to 41 per hour. This position may present an opportunity to go permanent.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success
Requirements:
  • Technical writing skills
  • SOP writing
  • Training materials creation and delivery experience
  • eDMS use and administrative experience
  • Project management skills
  • Ability to work independently with minimal supervision
  • Able to shift priorities and manage more than one project at a time
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.

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