LSC are currently looking for a C&Q Lead to work client side on a global engineering team for large projects for our Cork based multinational Biopharmaceuticals client on a large project.
The C&Q Lead will have a key role in the Global team which is currently executing significant biologics projects. The Lead will be a key member of the project management team on a large capital project. The Lead may also work on smaller projects as needed by the business.
C&Q Lead Responsibilities are:
oEnsure there is a strong safety culture and performance in the execution of C&Q deliverables projects and that appropriate stage gate controls are in place prior to the commencement of C&Q activities
oAttends field walk downs as client C&Q Representative to ensure that appropriate standards are being met with installations
oEnsures that EPCM has appropriate stage gate approach in place to ensure rigour in allowing systems pass from Construction Completion to Energisation
oCoordinate a commissioning and qualification programme, incorporating utilities, cleanroom, upstream and downstream manufacturing equipment
oRepresent the Client and Coordinate the efforts of EPCM C&Q Team
oAssist in the development of C&Q plans and successfully execute them according to established schedule, cost and performance standards.
Attends and provides inputs to Interactive Pull Planning Workshops with stakeholders to plan out commissioning & qualification activities in a schedule critical project
oProvide technical support to the EPCM commissioning team throughout the project life cycle
oOversee via the EPCM the generation, execution and approval of Commissioning & Qualification documentation
oAssistance with management of changes in C&Q Phase with inputs to HAZOP and design reviews of proposed changes. Manage project changes and ensure all are captured, documented and assessed for Quality / Safety / Cost or schedule impact
The requirements for the C&Q Lead are:
oThird level degree in a relevant discipline
oProven level of experience in delivering Commissioning, Qualification & Validation (CQV) activities within the pharmaceutical sector
oExperience of working in a project environment
oAbility to sequence critical activities in planning work for C&Q Phase
oExperience of CSV an Advantage
oSome Knowledge of Temp Mapping an Advantage
Please contact James on 021 4777329 for full details on this role or apply directly through this advert.