Project Controls Lead
- North America, East Coast
- Contract
- Life Sciences, CAPEX Projects
This is a fantastic opportunity for a Project Controls Lead to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn.
Requirements:
- Establishing a One Team environment characterized by open, effective communication, collaboration, and respect for diverse experiences and ideas.
- Specifications for schedule certainty, specifically with the contractors that will deliver the work.
- Specifications for cost certainty, cost reduction, and cost controls
- Change control during design development to maintain target cost.
- Risk management for the lifecycle of the program.
- Processes for monitoring progress and/or earned value.
- Processes for effect invoice and payment application validation.
- Defining an effective program controls strategy and organization for the full project.
- Standardising data and reporting metrics using data visualization tools.
- Governance to ensure downstream project controls providers are delivering quality.
- Prepare schedule baseline based on various stages of basic and detailed design in Primavera P6.
- Develop and maintain master schedule, cost loading of the schedule in accordance with contractual requirements and ensures project updates reflect actual site conditions.
- Define, develop and document multiple dependent or independent budgets; work breakdown (WBS) and cost coding structures; approved changes to baselines for new forecast dates and performances.
- Monitor end-to-end longest path of all disciplines to make sure the critical tasks are following the logic and flow chart.
- Prepare bi-weekly and monthly progress reports, schedule deviations, and mitigation plan, look ahead, resources, monitor and track any critical and high-risk activities.
- Extensive project management experience within pharmaceutical, biotech, or life sciences environments
- Proficiency in Primavera P6 for project scheduling and resource planning
- Strong understanding of cGMP regulations, validation processes, and FDA regulatory requirements
- Experience managing capital projects, construction, and commissioning in a pharmaceutical manufacturing setting
- Proven ability to lead cross-functional teams and manage budgets, timelines, and project deliverables
- Strong written and verbal communication skills for interfacing with stakeholders, contractors, and site teams
- PMP certification or similar is preferred
#LI-KS1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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