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Bioprocess Associate Downstream

  1. Dublin
County Dublin
  1. Contract
Competitive
  1. CAPEX Projects
34619

This vacancy has now expired

Bioprocess Associate Downstream - Dublin, Ireland - 12-Month Contract 

One of the top 10 best companies to work in Ireland is looking for more engineers for their large-scale new facility north of 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.


Key duties: 
  • Working with the manufacturing operations group, project design team, the CQV team, & the Automation/CSV reps to facilitate the implementation of the project design and validation of the MPCC manufacturing facility.
  • Creation of operating procedures & other relevant documentation for large scale manufacturing
  • Execution of commercial manufacturing processes according to established work instructions.
  • Adheres to Good Manufacturing Practices and Standard Operating Procedures.
  • Takes part in investigations and optimisation's of processes using scientific, engineering and lean principles
  • Operates all production equipment within the assigned functional area
  • Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.).
  • Assists with reviewing batch and exception reports for each manufacturing lot in conjunction with Quality representative and provide input to related investigations and QA audit activities.
  • Engages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and safe work environment.

Qualifications, skills, and knowledge: 
  • 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.

If this role is of interest to you, please apply now! 
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