Project Engineer

Quanta part of QCS Staffing
Maryland
Temporary

Project Engineer - Pharmaceuticals - Maryland - 12-Month Contract

This is a fantastic opportunity for a Project Engineer to join our major, global pharmaceutical client on their latest new-build project based in Maryland, this is a large-scale greenfield capital project and investing more than $1bn.

Responsibilities :

  • Collaborate with project stakeholders to define project requirements, objectives, and deliverables.
  • Manage the day-to-day activities of the construction site, ensuring adherence to safety, quality, and regulatory standards.
  • Coordinate with contractors, vendors, and subcontractors to ensure timely delivery of materials and services.
  • Monitor project progress, identify potential risks or issues, and implement corrective actions as necessary.
  • Review and approve construction plans, drawings, and specifications to ensure compliance with project requirements.
  • Prepare and maintain project documentation, including progress reports, meeting minutes, and change orders.
  • Participate in regular meetings with project team members to provide updates on project status, milestones, and issue resolution.
  • Assist in the evaluation and selection of contractors and suppliers, ensuring alignment with project objectives and budgetary constraints.
  • Support commissioning and startup activities, including equipment testing, validation, and qualification.

Qualifications :

  • Must have experience working for a general contractor or construction management company.
  • Must have 5 years of experience in construction or CAPEX projects, preferably within the pharmaceutical, oil and gas, or chemical industries.
  • Proven track record of successfully managing construction projects from conception to completion.
  • Strong understanding of construction processes, techniques, and best practices.
  • Ideally has experience with estimating.
  • Bachelor's degree in Engineering, Construction Management, or a related field.
  • Familiarity with regulatory requirements and standards applicable to pharmaceutical manufacturing facilities (e.g., FDA, cGMP).
  • Excellent communication, leadership, and interpersonal skills.
  • Ability to work effectively in a fast-paced, dynamic environment.
  • Willingness to be site-based in Lebanon, Indiana, for the duration of the project.

If this role is of interest to you, please apply now!

LI-AN1

30+ days ago
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