US Compounding
  • Conway, AR, USA
  • Hourly
  • Full Time

medical, life, 401k, disability, vision, dental


  • Perform quality control activities ensuring adherence to company policies and procedures.



  • Perform all environmental and personnel monitoring in the sterile suite
  • Read sampling results & notify appropriate personnel of excursions
  • Assist with environmental monitoring investigations, data entry, and trending analyses
  • Understand overall Quality Management System and promote a culture of quality and continuous improvement as a member of the Quality Team.
  • Review and approval of environmental trending data.
  • Author revise and train on SOP's, protocols and reports.
  • Monitor that equipment PM's and calibrations are completed within required timeframes.
  • Other duties as requested by supervisor.

MINIMUM QUALIFICATIONS (applicants who do not meet these will not be considered)

  • Bachelor's Degree in a scientific field or Technical College Degree in a related area of expertise with at least 2 years' experience in cGMP manufacturing, quality assurance or quality control role.
  • Quality experience, knowledge of good documentation practices, and basics understanding of cGMP compliance required.


  • Attention to detail and the ability to assess, review and approve generated data, batch records and SOP's
  • Ability to work independently, open to seeking guidance when necessary and the ability to be a self- starter.
  • Ability to manage multiple complex and varied tasks with enthusiasm
  • Flexible attitude, capable of training, mentoring quality staff and others to promote Quality
  • Previous experience with electronic QMS including controlled documents and training.
  • Capable of communicating and negotiating to meet the required quality requirements
  • Possess the ability to work individual and in team environment to meet Quality objectives
US Compounding
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