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PerkinElmer

Project Controls Engineer III

PerkinElmer

. Support biomanufacturing projects across the entire engineering lifecycle .

Posted 11/10/2026full-timeRemote • North Carolina • United StatesJuniorMid-Level💰 $74,000 - $95,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in biomanufacturing project controls, including project scheduling, performance monitoring, and data analysis. Proficient in cross-functional collaboration and delivering high-quality project deliverables within the life sciences and construction industries.

Highest-signal resume keywords
Project ControlsBiomanufacturingMicrosoft ExcelCGMP Facility Start-UpData Analysis

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project SchedulingPerformance MonitoringVariance ReportingBudget EstimationForecast Trend AnalysisQuality ControlRisk AnalysisChange Impact AnalysisActivity TrackingTechnical Aptitude
Soft Skills
CommunicationProblem-SolvingClient SupportCollaborationCreative Solutions
Tools & Technologies
Project Management SoftwareEnterprise SystemsGxP Automated SystemsDashboardsDeliverable Trackers
Industry Keywords
PharmaGeneral ConstructionRegulatory ComplianceQuality AssuranceEngineering Lifecycle

About the role

Key responsibilities & impact
  • Support biomanufacturing projects across the entire engineering lifecycle
  • Develop and maintain project schedules and monitor project performance
  • Interface with project management, client management, and site personnel to develop detailed integrated schedules
  • Deliver project controls outputs including project plans, milestone reports, execution schedules, activity tracking and variance reports, budget estimates, cost reports, forecast trend analysis, issue/risk/scenario analysis, scope and change impact analysis, and monthly project status reports
  • Analyze complex project data and deliver clear, concise messages to support decision-making
  • Align with cross-functional client departments including Design, Construction, Validation, Manufacturing, Quality, Supply Chain, and Engineering
  • Communicate project information internally and relay in-field project decisions and downstream impacts
  • Provide hands-on client support and troubleshooting for engineering lifecycle equipment and manufacturing processes
  • Maintain site dashboards, detailed schedules, and deliverable trackers
  • Perform due diligence and quality checks to generate high-quality project deliverables
  • Identify and escalate roadblocks and develop creative solutions
  • Support forecasted billables and monthly billable targets
  • Develop technical aptitude in life-science project controls, including CAPEX facility builds, shutdowns/turnarounds, technology transfers, enterprise system integrations, validation lifecycles, quality/regulatory/compliance, GxP automated systems, quality control, and operational readiness

Requirements

What you’ll need
  • Successful candidate will reside within 50 miles of Raleigh, NC
  • Bachelor’s Degree (and/or Masters) in technical Sciences, Engineering, Regulatory or related discipline OR a combination of equivalent experience in project controls, general construction, cGMP facility start-up, project management and/or comparable military experience
  • 2-4 years of experience required
  • Advanced experience with Microsoft Excel
  • Willingness to travel as required for client project assignments
  • Pharma and/or general construction industry alignment
  • Applicants must be authorized to work in the United States on a full-time basis
  • Employer will not sponsor current or future work visas
  • Cannot employ anyone with an invalid driver's license