PE Global is currently recruiting for a Bioprocess for a leading multi-national Biotech client based in Dublin West.
This is an initial 12-month contract position working on a 4 cycle 12-hour shift pattern.
ROLE:
* Deliver expert level of execution in manufacturing-process unit operations according to established standard work instructions
* Expert in operation of manufacturing equipment and technology within the functional area
* Technical author and approver for operating procedures & documentation for large-scale manufacturing
* Deliver expertise in training, training content design combined with oversight and approval of Manufacturing Specialist’s on-the-job training and competency
* Driving Right-First-Time execution on shift & front-line support/resolution of manufacturing issues
* Expertise in the use of process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and supporting business systems (i.e. SAP. Trackwise, Maximo etc.)
* Lead shift-based Investigations in QMS and drive effective CAPA implementation
* Oversee real-time review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance team and provide support to QA audit readiness activities
* Driving and promoting Good Manufacturing Practices Good Documentation Practices and adherence with Standard Operating Procedures
* Operating to and maintaining dynamic schedules – in a fast-paced production environment
* Facilitate and support change control and project changes to operations in the MPCC manufacturing facility in collaboration with the Manufacturing Operations group, Technical Transfer Teams,
* Manufacturing Engineers & the Automation teams
* Support for NPI execution activities and non-routine protocol activities
* Role model and support a culture of continuous improvement and operational excellence
* Ownership and promotion of improvement projects for manufacturing work practices and a safe working environment by application of sound scientific, engineering and lean principles
* Role model of the Site behaviours and Safety culture
REQUIREMENTS:
* The successful candidate will ideally possess a minimum of Level 6 qualification in an Engineering/Science related discipline; however, relevant experience in a similar regulated industry will also be considered (e.g. cGMP, ISO or similar cleanroom industry experience strongly preferred)
* Ideally possess 1-3+ years’ working experience in a large-scale biopharmaceutical manufacturing facility
* Experience with Delta V and MES would be considered an advantage.
* The successful candidate must demonstrate an ability to work independently and also as part of a team.
* The successful candidate must demonstrate problem solving ability and to adhere to scheduled timelines.
* Excellent communication skills and the ability to work in a cross functional collaborative environment are required.
Interested candidates should submit an updated CV.
Please click the link below to apply, call Seán on +353 21 4297900 or alternatively send an up to date CV to sean.molloy@peglobal.net
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***
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