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Process Design Leads - Drug substance start up


Summary Sheet: Science & Technology

    
Advertiser NameQuanta Consultancy ServicesAdvertiser Type:Agency
Classification:Science & TechnologySubclassification:
Country:IrelandLocation:Ireland
Language:English - United Kingdom (en-GB) Contact Name:>Jenny Latham
Employment Type:ContractWorkhours:Not Specified



Position: Process Design Leads - Drug substance start up


Description: One of the top 10 best companies to work in Ireland is looking for more engineers for their large-scale new facility in Dublin. Is this you?

Process Leads are is required to join a Global Pharmaceutical company located in Dublin.


This is an exciting project, there are lots of opportunities to learn new technology and develop current skills within a fast paced €700 million project. This fantastic client offers the opportunity to work within a large-scale environment with cutting-edge technology.

Responsibilities:


  • Support client side design team in its efforts associated with the new build Facility.

  • Support the client side design reviews in the area of Purification, cell culture or process support equipment with particular responsibility for Upstream and OR Downstream operations.

  • Support client side design reviews in the area of support operations.

  • Participate in cross-functional package, area, or overall design teams as required in support of the client's overall design goals and expectations.

  • Participate in design reviews, model reviews, etc., and to input on design technical elements.

  • Execute P&ID, URS, Specification and other reviews associated with the operations.

  • Provide input and assistance to both Automation and CQV in relation to operations.

  • Act as a secondary back-up to a colleague Process Engineering Area Lead.

  • Participate in the design reviews and specifications review of any Vendor Package Equipment in respective work streams.

  • Provide assistance for FAT's/SAT/CQV activities at various locations as required.

Requirements:


  • Extensive experience in GMP pharmaceutical design/build/commission/start-up with direct responsibility for Engineering Documentation, Project Execution or Facility Design.

  • Experience with design, construction or commissioning of a drug substance, drug product or finished product facility.

  • Direct experience in a similar scale project of Purification Operations.

  • Experience of Validation/Verification of GMP equipment or processes would be beneficial.

  • Demonstrated ability to organize and lead a multifunctional team in support of defined objectives.

  • Ability to constructively challenge, defend and present technical aspects of design and commissioning.

Please follow the links and apply for more information.






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