Reference Code
CK1140

Scheduler required for large contract at client site

Due to our continued success securing large scale projects, we wish to appoint a Lead Commissioning & Qualification (CQV) Scheduler for a large Bio-Pharmaceutical client project located in Cork. The Lead CQV Scheduler is a site based role for an estimated duration of 14 months with potential future opportunities thereafter.

Role and Responsibilities

  • Ensuring full and robust integration CQV schedule phase
  • On-going review and implementation of CQV schedule strategy as determined by CQV management
  • Liaise and work with CM Schedule teams
  • Ensuring on-time delivery of schedule deliverables
  • Planning, preparation and facilitation of key schedule workshops and communications
  • Compilation and issue of weekly and monthly schedule progress reports & graphics
  • Management of progress updating interface with CQV team weekly and monthly
  • On-going liaison with CQV team regarding schedule issues
  • Attendance and input at CQV progress meetings

Qualifications/Experience:

  • Minimum of a third level degree in a relevant discipline
  • 8 years’ experience In Planning / Scheduling with at least 3 years’ experience on Bio-Pharmaceutical projects (ideally in a Commissioning phase role)
  • Proficient in the use of Primavera P6, Microsoft Excel and Microsoft PowerPoint
  • Good communication & people skills
  • Good time management skills
  • Self-starter and decision maker

This is an urgent requirement and we would be delighted to hear from anyone who has large-scale scheduling experience.

Please Note

All CV’s are treated in the strictest confidence.
Recruitment agencies need not apply.

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Lead CQV Scheduler (CK1141) - CK1140

Cork Ireland

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