Quality Manager (2nd Shift & 3rd Shift) - Farmington, CT

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Job Description

Position Summary:

The Quality Manager will be responsible for the day to day operational function of the quality control process. The Quality Manager demonstrates a commitment to cGMP, SOP’s, quality and GDP to ensure conformance to standard practices.

Key Activities:

  • Provide overall supervision during 2nd shift operations.
  • Covers Quality Supervisor and Tech job functions in their absence.
  • Must be hands on.
  • Experienced reading and writing SOP’s
  • Ability to make systematic changes on our processes
  • Directs and trains QC techs engaged in inspections and sampling activities.
  • Plans, promotes and organizes training activities related to product quality and reliability.
  • Respond to, research and provide corrective actions to customer complaints regarding quality.
  • Ensure Quality Tech in process paperwork are accurate
  • Supervise, train and assign work to Quality Control.
  • Assist in the training activities related to product quality and reliability.
  • Responsible for hiring and discipline all employees
  • Instill quality standards set forth in SOPs and cGMP.
  • Review batch records in process for accuracy. Close out batch records with 24 hours of receipt.
  • Check in batch folders for accuracy.
  • Interact and provide quality control guidance to the production workforce.
  • Review and performs audits
  • Release Finished Product and Raw Material Releases.
  • Ability to work independent and communicated well with other.
  • Other job duties as required         
Required Qualifications:
  • Bachelor’s Degree or higher or commensurate experience (minimum 3 years).
  • At least 3-year experience with a Quality Team in the Dietary Supplement, Pharmaceutical, Food or closely related industry.
  • Previous experience in an FDA inspection facility is desirable.
  • Applicable experience and knowledge of cGMP and FDA regulations under 21 CFR 111.
  • Prior management experience is advantageous.
  • Ability to analyze records with a high level of accuracy.
  • Working knowledge of MS Office and Outlook.
  • Experience in a production environment strongly recommended.

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Details

Posted: Sep 06, 2018

Type: Full Time

Category: Quality Quality Manager Assurance GMP FDA