QC Supervisor

This American pharmaceutical company is one of the largest organisations of its kind globally. Their products cover a range of areas including heart and lung health, care for women’s health, cancer treatment, infectious diseases and many more disease areas. They employ 70,000 employees worldwide- 2,300 of which are employed directly, 9,000 indirectly in Ireland. They operate across 8 sites in Ireland.

The Position

This QC Supervisor role will be responsible for the supervision and co-ordination of Quality laboratories and personnel activities and to ensure the timely and efficient testing and reporting of QC samples.

  • Co-ordination of area resources.
  • Ensure testing is completed within required time frames
  • Supervision of area personnel.
  • Training of area personnel.
  • Participate in corporate/regulatory audits.
  • Delivery of area performance to meet or exceed performance or quality goals.
  • Contribute to site management operational and strategic initiatives.
  • Liaising with external vendors.
  • Ensure compliance with cGMP and other business compliance regulations.
  • Lead, promote, participate and supervise the implementation and maintenance of the SHE programmes relevant to you.
  • Participate in risk assessments, inspections, audits, incident investigations, etc. and implement and follow-up CAPA’s assigned to you.

The Person

The successful QC Supervisor should have the following:

  • Degree in Biological Sciences, Biochemical engineering or related.
  • 3-5 years’ experience working within the Biopharmaceutical or Pharmaceutical industry sectors -preferably in a manufacturing setting.
  • Experienced in cGMP.
  • Report, standards, policy writing skills required.

To learn more apply on line or call Preneta Naidoo on +353 1 6321870.

Salary: On Application Location: Cork