Structural Engineer

We are seeking an experienced and detail-oriented Structural Engineer to join our team for a pharmaceutical manufacturing facility build project. The ideal candidate will have a solid background in structural engineering, particularly in the design and construction of industrial or pharmaceutical facilities. You will be responsible for ensuring the structural integrity, safety, and compliance of all construction activities, working closely with multidisciplinary teams to deliver a highly regulated, GMP-compliant environment.

Key Responsibilities

  • Design and Analysis:
    • Perform structural analysis and design for foundations, steel, and concrete structures specific to pharmaceutical manufacturing facilities.
    • Design structural systems to support mechanical, electrical, and process equipment, ensuring compliance with all relevant codes and standards (e.g., ASCE, AISC, ACI, IBC).
    • Evaluate load-bearing structures, including seismic, wind, and vibration analysis, ensuring the facility meets stringent operational and safety requirements.
    • Collaborate with architectural, mechanical, and process teams to integrate structural designs with overall facility plans.
  • Project Coordination:
    • Work closely with project managers, architects, and other engineering disciplines (mechanical, electrical, process, HVAC) to ensure seamless integration of structural elements into the overall project design.
    • Coordinate with external consultants, contractors, and vendors to ensure alignment with project goals and timelines.
  • Construction Oversight:
    • Oversee and inspect construction activities to ensure structural systems are built according to the approved designs, specifications, and regulations.
    • Provide technical guidance and troubleshooting during construction, addressing site issues and ensuring compliance with structural requirements and safety standards.
  • Documentation and Compliance:
    • Prepare and review detailed engineering reports, construction drawings, and technical specifications for structural components.
    • Ensure all structural designs and processes comply with local building codes, industry standards, and GMP (Good Manufacturing Practice) regulations required for pharmaceutical facilities.
    • Develop and maintain engineering documentation, including calculation packages, design changes, and as-built records.
  • Risk and Safety Management:
    • Perform risk assessments for structural systems, identifying potential issues that may affect the integrity or safety of the building or equipment.
    • Ensure all structures support the hygienic and safety needs of a pharmaceutical environment, such as load-bearing support for cleanrooms, sterile environments, and heavy equipment.
  • Material and Cost Optimization:
    • Select appropriate building materials for structural integrity, corrosion resistance, and long-term performance in compliance with pharmaceutical industry standards.
    • Assist in preparing cost estimates, budgets, and timelines for the structural portion of the project.
  • Quality Assurance:
    • Implement and adhere to stringent quality control processes throughout the design and construction phases.

Ensure all inspections and testing of structural elements are completed, documented, and compliant with regulatory guidelines.

Requirements

Qualifications

  • Bachelor’s or Master’s Degree in Structural Engineering or Civil Engineering (with a structural focus).
  • Minimum of 10 years of experience in structural engineering, preferably within industrial or pharmaceutical manufacturing facility projects.
  • Professional Engineer (PE) license required.
  • Familiarity with GMP requirements is a plus.
  • Proficiency in structural analysis and design software (e.g., STAAD, ETABS, SAP2000, RISA, AutoCAD, Revit).
  • Strong knowledge of building codes (e.g., IBC, ACI, AISC, ASCE) and pharmaceutical facility regulations.
  • Experience in seismic, wind, and vibration design and analysis.
  • Familiarity with the unique requirements of pharmaceutical manufacturing facilities (e.g., cleanrooms, contamination control, FDA, EMA regulations) is highly desirable.

Soft Skills

  • Cross-Cultural Communication
  • Adaptability and Flexibility
  • Team Collaboration and Interdisciplinary Skills
  • Problem-Solving and Critical Thinking
  • Emotional Intelligence
  • Time Management and Prioritization
  • Ethical Awareness and Sustainability Focus
  • Conflict Management
  • Stakeholder Engagement
  • Continuous Learning Mindset
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General Information

Vacancy: 009
Location: Europe
Contract type: 1 year rolling contract, consulting contract.
Project duration: 1-2 years.

How to Apply?

If you’re interested in this role, we’re looking forward to hear from you! Kindly apply via the JTR Consultancy Services website with your CV in Word Document version – one of our Business Development Managers will be in touch with you shortly.