Develop comprehensive architectural designs for pharmaceutical facilities (API and formulations), including detailed interior layouts.
Expert in AutoCAD software with knowledge of advanced standards and practices.
Ability to create detailed 3D visualizations for architectural concepts. Specialized in 3D visualization and work as an architectural expert, applying architectural concepts within the pharmaceutical industry to create realistic and functional designs
Integrate various pharmaceutical process equipment into facility layouts, ensuring optimal space utilization and workflow efficiency.
Able to act as SME for facility and architect in formulation pharmaceutical industry (Sterile and non-sterile)
Expert in personnel, material, and waste flow concepts to create efficient and compliant layouts considering the containment and regulatory requirements.
Understand cleanroom area classification, pressure cascading and HVAC zoning to ensure regulatory compliance and operational efficiency.
Able to assess and plan room size requirements for different process rooms, ensuring sufficient space for equipment and operations.
Understand the functions and dimensions of various pharmaceutical process equipment and associated systems used in the Sterile, OSD and API facilities.
Should have good knowledge on CapEx related cost estimation.
Capable to select/propose solutions and alternatives with proper justification and without any deviation.
Your experience and qualifications
Bachelor s degree in engineering or equivalent and Certification course in AutoCAD, Revit etc
10+ years of experience in design, engineering, consulting, construction and in commissioning of sterile and non-sterile facilities in Pharmaceutical Industry.
Working experience in consulting is preferred
Proven track record of working on pharmaceutical projects, demonstrating a deep understanding of industry-specific requirements and standards.
Extensive experience working on international projects, particularly in Europe and the US.
Familiarity with current pharmaceutical guidelines and standards, including ISPE, ISO, and clean room guidelines.
Thorough understanding of regulatory compliance requirements, including Good Manufacturing Practices (GMP) and Environmental Health and Safety (EHS) standards.