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Experis

Quality Documentation Associate (Pharma/Device)

Post Date:Jan 02, 2018Type:Full-Time
Start Date:1/2/2018Salary:
Location:US-IL-Northbrook Job Reference:FOX_11288273
Skills:
 

Job Description:

Quality Documentation Associate

Pharmaceutical / Medical Device Industry

Primary Responsibilities:

The Quality Documentation Associate will support change control documentation for pharmaceutical & medical device products in accordance with company policy and procedures. Individual will be working cross-functionally with Regulatory, Documentation, Labeling, Scientist, and Validation groups.

Qualifications:

  • Experience within the pharmaceutical or medical device industries is required.
  • Bachelor's degree in life science or related field preferred.
  • Prior work experience managing QA Documentation.
  • Prior experiencing working in a GMP environment.
  • Experience with Electronic Document Management systems.

Experis is an Equal Opportunity Employer (EOE/AA)





Contact Information
Experis
Name: Experis


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