Description
A Global generic pharmaceutical company based in Dublin is seek a QP to join their team.Working in a busy environment for Qualified Person role your duties will include;
- To release clinical trials and finished product manufactured to the clinic / 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, nonconformance issues and request follow up.
- To perform risk assessments where required with respect to use of Clinical Trial Material.
- 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.
- Some travel will be expected as part of this role.
Here are the qualifications required for this position:
- Third level qualification in a science related discipline
- Qualified Person qualification for Biologics / Injectables
- Strong organizational skills with the ability to multitask and prioritise workload
- At least 5 years' experience in Biologics / Injectables pharmaceutical manufacturing
If you are interested in this exciting opportunity please contact me Anna Mooney or apply below with an up to date CV.