Role Responsibilities
- Manage small team of C&Q Engineers on a client site, on multiple concurrent minor/medium size projects, throughout the project lifecycle, as part of the Overall Engineering Service Provider Team.
- Produce estimates for C&Q activities for each project and ensuring adherence to these estimates
- Strong experience with Validation Master Plan, Commissioning Planning, project procedures and commissioning and qualification
- Design Review (DR) process and GMP Risk Assessment experience
- Identify the appropriate Commissioning and Qualification strategy to apply on specific projects and define the list of activities required
- Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirements
- Investigate and resolve technical issues with assistance from our client’s engineers and/or suppliers
- Ensure site project execution is undertaken in compliance with site procedures and safety standards
- Be familiar with Mechanical/E&I Completion procedure and Construction scopes of work
- Schedule preparation and progress review
- Organize and review daily activities of other CQV Engineers assigned to the projects
- Project management principles to coordinate CQV activities and reporting to our client
- Change Management activities during project lifecycle
- Production and execution of all types of CQV documents
- Final Handover reports
- Hands on approach required
Role Requirements
- Degree or equivalent in an engineering related discipline
- Experience in commissioning and qualification activities for pharmaceutical facilities/projects
- Strong leadership and team player ability, liaising directly with client and other project key functions
- Previous experience as manager/leader of C&Q team preferred
- Strong knowledge of ISPE and ASTM E2500
- Mentor for junior staff members
- Eligibility to work in Ireland
What’s in it for you?
- Competitive hourly rates
- Stable contract duration