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Quality Associate I

Round Lake, ILRandstad LifeSciences

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Job Title:  Quality Associate I

Position Description

  • Processing complaint files and/or MDRs.
  • Managing a complaint file and/or MDR workflow, which includes performing the daily tasks associated with processing these files.
  • Participate in continuous improvement efforts and projects.
  • Assist in developing plans to investigate identified risks.

Position Responsibilities

  • Interpersonal skills
  • Ability to prioritize and multitask
  • Collaboration and Teamwork
  • Detail Oriented
  • Proficient with computers
  • Customer Focus

Position Requirements

  • Minimum of an Associate’s Degree required in nursing, pharmacy, medical technology, engineering or scientific background (MLT, LPN, RN) or equivalent experience (defined as a minimum of 3 years of medical products industry experience).
  • Bachelor degree and/or clinical certification (MT, RN) preferred.
  • 0-3 years work experience in a cGMP related industry or in a clinical setting
  • Project Management experience and/or certification preferred.


  • Medical, Dental, and Vision Insurance
  • 401K Plan with Company Match
  • Flexible Spending Account
  • Life and AD&D Insurance

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