QC Analyst

On behalf of our Pharmaceutical Manufacturing company in Cashel, Co Tipperary, we are recruiting for a QC Analyst to join their Team.

Job Responsibilities:

• Prepares Laboratory procedures, specifications, protocols & reports as required

• Performs Laboratory testing and investigations per SOP, applicable regulations and cGMP

• Performs peer review of documentation as required

• Performs Analytical method verification, validation and technical transfer as required

• Supports Laboratory/Site EHS governance

• Performs management of Laboratory consumables ordering and tracking

• Assists in Equipment Qualification activities, ordering and tracking as required

• Supports Laboratory colleagues on a day to day basis

• Supports preparation for regulatory audits/visits ad ongoing audit readiness

• Supports development of QC Testing processes

• Report problems with quality, processes and materials to the HOD.

• Work closely with support staff such as technicians, Engineering, Operations Head/designee, Materials/Warehouse.

• Follow documented policies and procedures as designated by the company’s Quality Management System.

• Complete required documentation relating to business and regulatory requirements and as per Good Documentation Practice procedures.

• Performs analytical balance calibrations, as and when required, as defined in relevant QC SOPs, once compliance to any training criteria set out in SOP QC046 (Analyst Qualification in the QC/ARD Laboratory) are met.

If you have the above experience working in a similar role, please contact catriona.duggan@cpl.ie or Tele: 087 2419644

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