Mechanical Engineer

We are seeking a skilled Mechanical Engineer to join our team for a pharmaceutical manufacturing facility build project. The successful candidate will play a key role in the design, installation, commissioning, and optimization of mechanical systems within the facility, ensuring compliance with pharmaceutical industry standards (GMP, FDA) and ensuring smooth project execution. You will work closely with a multidisciplinary team including architects, electrical engineers, process engineers, and contractors to deliver a state-of-the-art pharmaceutical facility.

Key Responsibilities

Design and Engineering:
- Develop and review designs for mechanical systems, including HVAC, plumbing, process piping, and utility systems.
- Create detailed technical drawings, specifications, and documentation to ensure compliance with pharmaceutical standards.
- Participate in design reviews and provide inputs to optimize mechanical systems for efficiency, safety, and cost.
Project Planning & Coordination:
- Collaborate with cross-functional teams (project management, architects, process engineers) to integrate mechanical systems into the overall facility design.
- Assist in developing project timelines, budgets, and procurement plans for mechanical equipment and materials.
- Review and approve mechanical design submittals from contractors and suppliers.
Installation & Commissioning:
- Oversee the installation and construction of mechanical systems, ensuring adherence to design specifications, safety standards, and regulatory requirements.
- Conduct site inspections and monitor progress, resolving issues or discrepancies during construction.
- Lead or support the commissioning and validation of HVAC, water systems, and critical utilities to meet GMP and FDA requirements.
Compliance and Safety:
- Ensure all mechanical engineering activities comply with Good Manufacturing Practices (GMP), FDA, and ISO regulations specific to pharmaceutical manufacturing.
- Conduct risk assessments and implement engineering solutions to address potential mechanical and process hazards.
- Collaborate with the quality assurance team to ensure that mechanical systems meet all validation requirements.
Troubleshooting and Optimization:
- Provide technical support and problem-solving expertise during construction and commissioning phases.
- Perform root cause analysis for mechanical system failures or issues and implement corrective actions.
- Continuously improve the design and operation of mechanical systems to maximize efficiency, reliability, and cost-effectiveness.
Documentation and Reporting:
- Prepare technical reports, operation and maintenance manuals, and validation protocols for mechanical systems.
- Maintain up-to-date project records, drawings, and equipment documentation.
- Provide regular updates to the project manager and stakeholders on project milestones and technical challenges.

Requirements

Qualifications

Bachelor’s degree in Mechanical Engineering or related field.
10+ years of experience in mechanical engineering, preferably in the pharmaceutical or biotech industry.
Proficiency in mechanical design for HVAC, process piping, and utility systems.
Familiarity with pharmaceutical facility requirements, including cleanroom environments, sterile processing areas, and critical utilities.
Knowledge of GMP, FDA, and ISO guidelines related to pharmaceutical manufacturing.
Proficient in CAD software (AutoCAD, SolidWorks, etc.) and other engineering tools for design and analysis.
Professional Engineering (PE) license is preferred.
Certifications in HVAC, cleanroom design, or pharmaceutical engineering (optional but beneficial)

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

Share this job

General Information

Vacancy: 004

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.