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QC Supervisor

Job description

Do you have 4+ years of QC supervisory experience? Would you like to make a positive impact on people's lives?

Job Responsibilities

  • Supervise the analyses of raw materials, bulk product & finished products
  • Coordinate activity of technicians & supervise the work performed
  • Ensure training of QC employees is carried out & adapted accordingly
  • Manage QC projects as required
  • Participate in recruitment activities & performance appraisals of employees
  • Review analytical data & approve & release materials
  • Organize necessary validations in compliance with national & international requirements
  • Participate in achievement of QC objectives & development plans, audits, and inspections
  • Report management- monthly, quarterly, KPI, etc
  • Develop technical specification & project justification as required
  • Manage project schedule & key milestones
  • Delegate for QC Managers, as required

Job Requirements

  • 3-5 years’ supervisory experience in a QC laboratory within a Pharmaceutical environment
  • Ability to provide direction, motivate others, management control, concern for excellence
  • Knowledge of QC Regulations & EU & FDA Regulations
  • Knowledge of FLI manufacturing processes & practices is an advantage
  • Experience using ERP computerized solutions

For a confidential discussion on this or any other current job opportunity please contact Meggan on 021 235 9144 / mtully@sigmar.ie

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