Description
Global healthcare company is seeking a QP to join their team within their North Dublin site.Day to Day:
- To release product manufactured to market as required under the EU Directive /EC
- To assist in the coordination of the QA duties relating to the dispatch of goods.
- To review all relevant documentation relating to product released to the market.
- To highlight deviations, non-conformance issues and request follow up.
- To ensure release procedures comply with regulatory and company requirements
- To act as change agents by gaining support for and driving sustainable improvements to ways of work
- Technical Transfer and Process Validation Support
- Liaise with Clinical, Third Party Release and Re-packaging agents as required.
Requires:
- Third level qualification in a science related discipline
- Qualified Person qualification Strong organizational skills with the ability to multitask and prioritise workload
- Minimum of two year's experience in a QP role, listed on a MA
- Experience in Sterile and/or Biologics pharmaceutical manufacturing an advantage
If you are interested in this great opportunity and have the appropriate skill set and experience please contact me Anna Mooney or apply below with an up to date CV.