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BioProcess Associate

  1. Ireland, Dublin
Dublin
  1. Contract
Competitive
  1. Life Sciences
36205
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BioProcess Associate - Dublin - 12 Months

One of the top 10 best companies to work in Ireland is looking for BioProcess Associate 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:
  • Execution of commercial manufacturing processes according to established work instructions
  • Creation of operating procedures & other relevant documentation for large scale manufacturing
  • Operating production equipment within the assigned functional area
  • Adhering to Good Manufacturing Practices and Standard Operating Procedures
  • Taking part in investigations and optimisation of processes using scientific, engineering and lean principles
  • Proficient use of process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.)
  • Assisting with review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative and provide input to related investigations and QA audit activities
  • Working with the manufacturing operations group, the project design team, the CQV team, & the Automation/Computer Systems Validation teams to facilitate the implementation of the project design, validation and operation of the MPCC manufacturing facility
  • Engages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and a safe working environment
Key requirements include:
  • 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)
  • Working experience in a large-scale biopharmaceutical manufacturing facility would be a distinct advantage
  • Experience with Delta V and MES or similar control and data acquisition systems would be desirable
  • The candidate must demonstrate an ability to work independently and also as part of a team.
  • A successful candidate will have a demonstrated problem-solving ability and the ability to adhere to scheduled timelines
  • Excellent communication skills and the ability to work in a cross-functional, collaborative and fast-paced environment are essential

If this role is of interest, please apply now!

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