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CIP C&Q Lead

  1. Dublin
County Dublin
  1. Contract
Competitive
  1. CAPEX Projects
34432

This vacancy has now expired

CIP C&Q Lead - Pharmaceuticals - Dublin, Ireland - 12-Month Contract 
 
Do you want to work with an exciting company who are an established market leader within their niche field? We have a fantastic opportunity for a CIP C&Q Lead to work on an exciting CapEx project in Ireland on an initial 12-month contract.


Essential Duties and Responsibilities:
  • Plan and lead team of engineers in commissioning and qualification CIP systems.
  • Plan and lead team of engineers in completing hydraulic balancing of CIP.
  • Liaise and coordinate CIP testing activities with other system owners to ensure CIP testing meets schedule requirements.
  • Participate in design document reviews and ensure that quality aspects are included in design.
  • Attend FAT and execution of agreed testing protocols and sign off on permission to ship forms.
  • Generate CQV documents at project level and for specific equipment/systems. Liaising with Quality, Engineering and CQV to align on Critical parameters and document content.
  • Work with the automation teams, ensure that process descriptions are provided, and Functional Specs are reviewed and approved to ensure that the automation element of the project meets schedule.
  • Track and confirm closure of actions items identified through FAT, HAZOP, Design Qualification and other reviews.
  • Maintain a strong interface with the Automation and Engineering teams to ensure that the information flow meets the needs of the Automation and Engineering teams, resolving issues as they arise.
  • Participate in construction system completion walkdowns.
  • Coordinate and lead team of shift C&Q engineers in the execution of commissioning, cycle development and shakedown activities.
  • Perform shakedown and commissioning and qualification of systems.
  • Introduce caustic to CIP skids and oversee safe use of caustic in cleaning cycle development.
  • Oversee cycle development of cleaning cycles to reduce caustic concentration to acceptable levels.

Requirements:
  • B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
  • Extensive experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
  • Experienced in commissioning and qualifying CIP systems.
  • Experienced in leading teams of engineers.
  • Demonstrated ability to work on own initiative and proactively respond to business needs.
  • Excellent interpersonal and communication skills.
  • Familiar with Delta-V & Navis Works an advantage.

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

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