AutoCAD Engineer

We are seeking a highly skilled AutoCAD Engineer to join our team for a Pharmaceutical Manufacturing Facility build project. The AutoCAD Engineer will be responsible for creating, modifying, and managing detailed 2D and 3D design drawings for the construction and layout of the facility. You will collaborate with architects, process engineers, mechanical engineers, and project managers to ensure that the facility design adheres to project specifications, industry standards, and regulatory requirements specific to the pharmaceutical sector.

This role demands excellent attention to detail, knowledge of cGMP (Current Good Manufacturing Practices), and a strong ability to collaborate across multiple disciplines.

Key Responsibilities

  • Drafting & Design:
    • Develop detailed 2D and 3D AutoCAD drawings for the layout, piping, HVAC, electrical systems, equipment placement, and structural designs specific to pharmaceutical manufacturing facilities.
    • Convert conceptual designs into detailed, production-ready drawings.
    • Ensure that all designs meet industry standards, local building codes, and regulatory requirements (e.g., FDA, EMA, etc.).
  • Coordination with Cross-Functional Teams:
    • Collaborate closely with project architects, process engineers, electrical and mechanical engineers, and contractors to integrate all disciplines into the design.
    • Ensure seamless alignment between design, equipment placement, and facility processes.
    • Participate in design reviews and project meetings to provide insights and resolve design challenges.
  • Compliance & Documentation:
    • Ensure that designs adhere to cGMP standards and pharmaceutical regulations, including contamination controls, cleanroom standards, and equipment integration.
    • Maintain accurate, organized, and up-to-date AutoCAD files and associated documentation.
    • Assist in the preparation of technical documentation and as-built drawings upon project completion.
  • Problem Solving & Modifications:
    • Identify and resolve design conflicts or discrepancies during construction, coordinating with other engineering disciplines to provide solutions.
    • Make adjustments to drawings as required by project changes, field conditions, or evolving client needs.
  • Site Support:
    • Provide technical support during the construction phase, ensuring that designs are followed accurately.
    • Conduct periodic site visits to verify that the construction is adhering to the design and address any design-related issues that arise on-site.
  • Software Proficiency:
    • Utilize AutoCAD and other relevant design software to produce high-quality drawings.
    • Maintain knowledge of the latest software updates and best practices for efficient design processes.

Requirements

Qualifications

  • Bachelor’s degree in Mechanical Engineering, Civil Engineering, or related field. An equivalent combination of education and experience may be considered.
  • 10+ years of AutoCAD drafting/design experience, with a focus on pharmaceutical, biotechnology, or other cleanroom manufacturing facilities.
  • Familiarity with pharmaceutical manufacturing equipment and facility requirements (e.g., process flow, HVAC, cleanroom design).
  • Proficiency in AutoCAD 2D/3D is required.
  • Experience with Revit, Navisworks, and other BIM (Building Information Modelling) software is a plus.
  • Strong understanding of cGMP, FDA, and international pharmaceutical facility regulations.
  • Strong ability to produce accurate, precise, and high-quality design work.
  • Effective communication skills to work with cross-functional teams and provide design feedback.
  • Ability to troubleshoot design issues and implement changes effectively.
  • Basic understanding of project timelines, milestones, and resource management.

Preferred Qualifications

  • Experience working on large-scale pharmaceutical or biotech facility projects.
  • Knowledge of cleanroom classifications, pressure differentials, and sterile manufacturing environments.
  • Familiarity with HVAC, piping, and instrumentation drawings (P&ID) specific to pharmaceutical environments.
  • Project management experience or certification (e.g., PMP) is an asset.

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: 011
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.