Description
My client is a global Bio-tech company based in Waterford is seeking a QA Specialist.Working as part of the Quality Assurance team you will be involved in supporting the day to day activities in Quality Assurance Department ensuring compliance in accordance with cGMP.
Some of the accountabilities:
- Perform critical / constructive review of documentation and practices.
- Effective coordination and communication of adherence to schedules
- Critical and constructive review of investigation reports
- Co - ordinate and participate in internal audits and key quality initiatives as appropriate.
- Work with relevant departments to ensure timely closure of quality actions / findings.
- Measure and report RFT data and work with departments to resolve recurring issues.
- Actively contribute to continuous improvement initiatives.
Experience
- Minimum of 3-6 years experience in a similar role.
- Experience working in a GMP environment is required.
- Technical writing and proven experience in report writing is required
- Problem solving skill desirable
- Third Level qualification (degree in science or related discipline preferred).
If you are interested in this great opportunity please contact me Anna Mooney or apply below in an up to date CV.