This is a critical role required to support an expansion project within a well-known Bio-facility in Cork.
You will need significant experience of Process Design through to Commissioning OQ Complete phase gained at Project co-ordination level on big CAPEX Projects within Drug Substance, API Single use environment.
This role is 100% on site which may require some EU/US travel (minimal).
Role:
* Responsible for the Process design and commissioning & qualification of a significant expansion to an existing bulk vaccine processing facility.
* Equipment package design, factory acceptance testing, installation and commissioning.
Packages may include Product Vessels, Single Use Mixers, Single Use UFDF skids & CIP/SIP skids.
* Lead cross-functional project teams to ensure project and site stakeholder inputs and requirements are clear and reflected in C&Q deliverables.
Education:
* Minimum qualification B.Sc. or M.Sc./M.Eng Degree in Chemical or Biochemical Engineering or equivalent discipline; equivalent is defined as a Biotechnology or Industrial Chemistry Degree with basic elements of chemical/biochemical engineering fundamentals as applied to biotechnology/bioprocessing.
* Minimum of 8 years post-academic process engineering experience in relevant biopharmaceutical processing design, construction & start-up environment.
* Demonstrated ability to lead/influence teams in a matrix team environment.
* Excellent communication/presentation/organizational skills.
* In-depth understanding of process engineering and technologies pertinent to unit process and utility operations for a bulk vaccine/biologics processing facility.
* Knowledge on the application of single-use technologies.
* Knowledge of DCS/PLC process control platforms and industry SDLC methodology such as Delta V.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Engineering, Design, and Manufacturing
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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