Project Controls Engineer III

This is a fully remote position, open to applicants in North Carolina.

📋 Description

• Provide support for biomanufacturing initiatives throughout all stages of the engineering lifecycle.

• Create and uphold project timelines while tracking overall project performance.

• Collaborate with project management, client representatives, and onsite personnel to formulate detailed integrated schedules.

• Produce project controls deliverables such as project plans, milestone reports, execution schedules, activity tracking, variance reports, budget estimates, cost reports, forecast trend analyses, issue/risk/scenario analyses, scope and change impact assessments, and monthly project status updates.

• Examine intricate project data and convey clear, succinct information to facilitate decision-making.

• Coordinate with various client departments, including Design, Construction, Validation, Manufacturing, Quality, Supply Chain, and Engineering.

• Relay project information internally and communicate in-field project decisions and their downstream effects.

• Offer hands-on assistance and troubleshooting for engineering lifecycle equipment and manufacturing processes.

• Maintain site dashboards, comprehensive schedules, and deliverable trackers.

• Conduct due diligence and quality checks to produce high-caliber project deliverables.

• Identify and escalate obstacles while devising innovative solutions.

• Assist in achieving forecasted billables and monthly billing objectives.

• Cultivate technical knowledge in life-science project controls, including CAPEX facility constructions, shutdowns/turnarounds, technology transfers, enterprise system integrations, validation lifecycles, quality/regulatory/compliance, GxP automated systems, quality control, and operational readiness.

⛳️ Requirements

• The ideal candidate should reside within 50 miles of Raleigh, NC.

• A Bachelor's Degree (or Master's) in Technical Sciences, Engineering, Regulatory, or a related field OR a combination of equivalent experience in project controls, general construction, cGMP facility start-up, project management, and/or relevant military experience.

• 2-4 years of required experience.

• Proficient in advanced Microsoft Excel.

• Willingness to travel as necessary for client project assignments.

• Background in the pharmaceutical and/or general construction industry.

• Applicants must be legally authorized to work in the United States on a full-time basis.

• The employer will not sponsor current or future work visas.

• Employment is not possible for individuals with an invalid driver's license.

🏝️ Benefits

• Competitive salary and performance-based incentives.

• Comprehensive health, dental, and vision insurance.

• Retirement savings plan with company matching.

• Opportunities for professional development and career advancement.

• Flexible work arrangements to promote work-life balance.