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.
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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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