Civil Engineer

We are seeking a highly skilled Civil Engineer to join our team for the construction of a state-of-the-art pharmaceutical manufacturing facility. The Civil Engineer will be responsible for planning, designing, and overseeing construction and infrastructure activities, ensuring compliance with local regulations, industry standards, and the unique requirements of a pharmaceutical production environment. This role requires a strong understanding of the specialized needs of cleanroom and sterile environments, as well as utility systems and site development within the pharmaceutical industry.

Key Responsibilities

Design and Planning:
- Develop civil and structural engineering designs, plans, and specifications in collaboration with architects, mechanical/electrical engineers, and other project stakeholders.
- Conduct feasibility studies, site evaluations, and environmental impact assessments to ensure appropriate site conditions for the facility.
- Ensure all civil engineering designs meet pharmaceutical industry requirements, including cGMP (current Good Manufacturing Practices) standards.
- Design infrastructure such as roads, drainage systems, underground utilities, and other site-related components essential for the manufacturing facility.
Project Management:
- Oversee and manage the execution of civil engineering projects from concept through completion, including permitting, bidding, and construction phases.
- Coordinate with contractors, subcontractors, and suppliers to ensure timely completion of civil works within budget.
- Review and monitor project schedules, ensuring alignment with overall construction timelines and quality control objectives.
Construction Supervision:
- Monitor construction activities and ensure compliance with the project’s technical specifications, health and safety regulations, and pharmaceutical standards.
- Conduct regular site inspections to ensure construction quality, adherence to drawings and specifications, and compliance with local building codes.
- Address engineering challenges and troubleshoot any issues arising during construction.
Regulatory Compliance & Safety:
- Ensure that all civil works adhere to local, national, and international building codes and environmental regulations.
- Collaborate with environmental engineers to ensure proper waste management, stormwater control, and erosion prevention strategies are implemented.
- Ensure the implementation of safety protocols to mitigate risks associated with the construction process.
Quality Assurance & Documentation:
- Prepare and review engineering reports, technical submittals, and drawings.
- Ensure proper documentation of civil engineering activities and maintain detailed project records.
- Assist in preparing as-built drawings and project completion reports.
Cross-Functional Collaboration:
- Collaborate with process engineers, mechanical/electrical teams, and quality control teams to ensure that civil works meet the operational needs of the pharmaceutical manufacturing process.
- Coordinate with HVAC and utility teams to ensure proper integration of facility services.
Risk Management:
- Identify potential risks related to site conditions, environmental factors, and project timelines, and propose solutions to mitigate these risks.
- Conduct structural integrity assessments and ensure the facility is prepared to meet pharmaceutical-grade standards.

Requirements

Qualifications

Bachelor’s degree in Civil Engineering or related field. A Master’s degree or specialization in structural engineering is preferred.
10+ years of experience in civil engineering, with specific experience in industrial or pharmaceutical manufacturing facilities being highly desirable.
Professional Engineer (PE) license or equivalent certifications.
Strong knowledge of building codes, cGMP regulations, and cleanroom construction standards.
Proficiency in civil engineering software such as AutoCAD, Civil 3D, or similar tools.
Excellent project management, problem-solving, and analytical skills.
Strong communication skills for cross-functional collaboration.
Familiarity with regulatory requirements, including environmental, safety, and health standards.
Experience in construction of cleanrooms and sterile areas.
Understanding of pharmaceutical manufacturing workflows and facility requirements.
Knowledge of green building principles and sustainable construction practices.
Ability to work on-site at the construction location.
Capable of conducting physical inspections, which may require walking, climbing, and standing for extended periods.

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: 005

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.