Job Description:
Working in a busy manufacturing environment your duties will include;
To release product manufactured along with third party manufacturing sites to market as required under the EU Directive 2001/83/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
Computer System Validation experience from Quality viewpoint is desirable
Skills / Experience:
Third level qualification in a science related discipline
Qualified Person qualification for solid dose
An understanding of, or exposure to Lean Manufacturing tools and techniques would be a distinct advantage
Strong organizational skills with the ability to multitask and prioritise workload
At least 2 years experience in Oral Solid Dosage pharmaceutical manufacturing
Please contact
tmurphy@brunel.ie or call 01-4485622