Manufacturing Scientist - Ireland, Dublin - 12 Month Contract
One of the top 10 best companies to work in Ireland is looking for aManufacturing Scientist for their large-scale new facility in Dublin. Is this you?
An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.
Responsibilities include:
* Contributes to cross functional team (Manufacturing, Engineering, QA, QC, Regulatory, Supply Chain, etc.) for process improvement implementations, new product start-ups or other process changes.
* Support new product introduction risk assessments to ensure the appropriate controls are in place to enable manufacturing
* Support product change over protocols to allow a smooth transition from sustaining to new product manufacturing
* Represent the Manufacturing at meeting to ensure the end user requirements are represented
* Supports process technology transfer, and the preparation of manufacturing documentation for development, engineering and PPQ batches.
* Identify process improvement projects for New Product Introduction and support projects to completion.
* Work with sustaining team to understanding current issues and ensure impact of new products are defined, agreed and understood
* Write process impact assessments to support new product introduction
* Provide SME input into cross-functional teams investigating & optimising new manufacturing processes, procedures and documentation.
* Provide training to BPAs on new procedures.
* Support external and internal audits.
* Work with cross-functional teams on the introduction of consumables and raw materials to support New Product Introduction .
* Work to implement a “Right-First Time Culture” and provide leadership in the use of OE principles.
* Support the disposition process when required
* Carry out organisational activities such as purchasing & co-coordinating communication information.
* Own & drive change controls, CAPA’s, investigations, improvement projects and operational safety.
Key requirements include:
* Ability to demonstrate proficiency communicating and collaborating at a variety of levels, coupled with excellent organisation and planning skills.
* In addition, must have proven success working in a team environment, as well as strong leadership & influencing skills, with flexibility to react to changing business needs.
* Problem solving and project management ability, as well as lean manufacturing experience is essential.
* Currently completing a Bachelors/Masters in Science, Engineering, or a related subject.
* In-depth theoretical knowledge of GMP biologics manufacturing equipment and process automation.
* Proven ability to support the closeout of complex technical investigations.
* Strong working knowledge of systems such as Delta V, MES Syncade and SAP.
If this role is of interest, please apply now!
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