Teva Sr Manager Process Architect Global Engineering 

India, Maharashtra, Navi Mumbai 

362624733

The role of the Process Architect is 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.

Act as SME for facilities and architecture to ensure that best-in-class facilities are planned and implemented at various Teva sites located across globe. Provide expert guidance and support to entire network to ensure the latest industry trends, technologies, and best practices are in place. 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. Develop and maintain engineering standards and procedures to ensure compliance with regulatory requirements and industry expectations

• Able to act as SME for facility and architect in API and formulation pharmaceutical industry (Sterile and non-sterile)
• Expert in AutoCAD software with knowledge of advanced standards and practices.
• Develop comprehensive architectural designs for pharmaceutical facilities (API and formulations), including detailed interior layouts.
• 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
• Create master plans incorporating both interior and exterior design elements to ensure functional and aesthetic coherence.
• Integrate various pharmaceutical process equipment into facility layouts, ensuring optimal space utilization and workflow efficiency.
• 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.
• Evaluate utility requirements from a conceptual perspective, enabling accurate room sizing based on utility needs.
• Working with cross functional experts to develop P&IDs for process, HVAC, critical utilities, electrical systems and plant utilities, ensuring precise and effective design.
• Draw ducting, piping, and cable layouts to facilitate efficient and organized utility distribution within the facility.
• Work closely with cross-functional teams to integrate equipment and utilities seamlessly into facility layouts.
• Standardize AutoCAD practices within the engineering department to ensure consistency and accuracy in design documentation.

• Conduct thorough facility assessments to maintain compliance with CGMP and other regulatory requirements.
• Should be able to execute and deliver strategic project phases like feasibility studies, conceptual design, FEED and Detail Design related to facilities planning in pharmaceutical industry independently.
• Must be able to prepare, review, comment and approve the engineering deliverables as per project specification, codes and standards.
• Should be able to collaborate with other discipline engineers, and design professionals like Process, HVAC, Utility, and Automation team, to create architectural deliverables that adheres to project specifications and standards/local requirements.
• Should have good knowledge on CapEx and OpEx related cost estimation.
• Capable to select/propose solutions and alternatives with proper justification and without any deviation.
• Proficient to prepare project execution strategy, schedule/timeline and monitor the progress as per the schedule.
• Should be capable to provide troubleshooting and corrective solutions.
• Capable to adhere to the strict deadline set by the global team, global business partners and project managers.
• Participation is every weekly/monthly/quarterly/half-yearly/yearly review meeting to update management about the progress, hurdles and next steps.
• Documentation: Maintain accurate and up-to-date project documentation, including design plans, layouts, vendor documentation, any deviations from the original plan.

• Bachelor’s degree in engineering or equivalent
• Certification course in AutoCAD, Revit etc
• 14+ years of experience in design, engineering, consulting, construction and in commissioning of sterile and non-sterile facilities in Pharmaceutical Industry.
• Working experience in manufacturing and 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.
• Rigorous, independent, and curious, with strong communication skills.
• Capable of managing projects in an international context, demonstrating persuasion and listening abilities

Sr Dir Regional Engineering I