Teva Manager - Design 

India, Maharashtra, Navi Mumbai 

951490348

The role of the Process Architect is responsible for designing of cleanroom facilities including equipment positioning, airlock systems, architecture finishes, building flows etc, ensuring adherence to TEVA and all applicable regulatory requirements.

Process Architect to serve as the expert in manufacturing facilities planning & designing with focus on layering the architecture, process equipment, utility systems and support infrastructure in accordance with current compliance requirements to deliver an integrated, compliant and efficient pharmaceutical manufacturing facility. Develop and maintain engineering standards and procedures to ensure compliance with regulatory requirements and industry expectations.

Act as SME for facilities and architecture to provide guidance and support to network sites to ensure that latest industry trends, technologies, and best practices are in place.

• 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.

• 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.