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Job Description
QC Analyst sought to prepare laboratory procedures, perform testing and investigations, and support laboratory governance in a pharmaceutical manufacturing environment.
Our Pharmaceutical Manufacturing company in Cashel, Co Tipperary, is 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.
- Manages Laboratory consumables ordering and tracking.
- Assists in Equipment Qualification activities, ordering and tracking as required.
- Supports Laboratory colleagues on a day-to-day basis.
- Prepares for regulatory audits/visits and maintains ongoing audit readiness.
- Supports development of QC Testing processes.
- Reports problems with quality, processes and materials to the HOD.
- Works closely with support staff such as technicians, Engineering, Operations Head/designee, Materials/Warehouse.
- Follows documented policies and procedures as designated by the company's Quality Management System.
- Completes 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.