Production

Bio-process Associate

  • Contract
  • West Dublin, County Dublin, Ireland
  • 42002153

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:

 

  • Minimum of Level 7 qualification in an Engineering/Science related discipline
  • Experience in a large-scale biopharmaceutical manufacturing facility
  • Competence with Delta V and MES or similar control and data acquisition systems would be required
  • Automation experience should include an ability to troubleshoot and run technical queries and reports in support of investigations and Data Integrity
  • Manufacturing and automation expertise and demonstrated ability to work independently and as part of a team.
  • Demonstrated problem-solving ability and the ability to work proactively to achieve demanding schedules
  • High proficiency in communication and collaborating at a variety of levels and the ability to work in a cross-functional and fast-paced team environment
  • Working flexibly to react to changing business needs.
  • Proven ability to support the close-out of complex investigations and good GMP awareness.
  • Proven ability to operate, maintain and troubleshoot bench analytical equipment supporting manufacturing processes

 

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***

By continuing to use the site, you agree to the use of cookies. More Information

The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.

Close