Quality Assurance Specialist – Tipperary/ Hybrid – Contract
Do you want to be part of one of the top 10 best pharmaceutical companies to work for in Ireland? We have a superb opportunity for a Quality Assurance Specialist to join our pharmaceutical partner, working at their facility in Co. Tipperary.
As a Quality Assurance Specialist, you will be involved with supporting all GMP Quality activities on site. This is a hybrid opportunity with a minimum of 1 day per week working on site.
Responsibilities as a Quality Assurance Specialist:
1. Review and approve production and analytical documentation accompanying the release of drug substance, drug product and packaged finished goods to ensure conformance to appropriate SOPs, GMP and regulatory requirements.
2. Perform and review complaints and deviation investigations, change controls and CAPA's.
3. Create and maintain assigned SOPs.
4. Compile data for reports and presentations, provide data interpretation and draw conclusions.
5. Complete audits.
6. Support product recalls and stock recoveries as appropriate.
Requirements for this Quality Assurance Specialist position:
1. A degree in a Science or Engineering discipline plus some industrial experience.
2. Alternatively, considerable industrial experience within Quality Assurance.
3. Batch record review experience and QMS experience is advantageous.
If this Quality Assurance Specialist position is of interest to you, please apply now
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