Live opening · Posted 11 days ago
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About the role
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Job title: Senior Drawer
Location: Hyderabad
About The Job
Our Team:
Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions.
As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health.
The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting M&S teams by acting as a crucial link between our R&D and Manufacturing facilities, playing a vital role in securing the present portfolio and delivering future launches of high-quality and innovative drugs and vaccines. The team members of the global M&S Services Hub will act as partners in carrying out tasks and fulfilling responsibilities to support global manufacturing sciences, analytics, and technology activities with a focus on global project management. Significant experience in the development of medical devices, drug device combination products and/or primary containers, and creation of Design Control documentation is necessary.
The Engineering organization is responsible for providing comprehensive Engineering support for GMP facilities across our global manufacturing sites. Our team:
Supports commercial manufacturing operations and Global Cell Banking operations
Maintains validated systems and ensures regulatory compliance
Provides engineering support for all cGMP process and utility systems
Manages facility planning and construction projects
Collaborates across campus/site organizations to ensure seamless operations
Main Responsibilities
CAD Design & Documentation
Prepare 2D/3D drawings using AutoCAD/Revit from redlines, sketches, and layouts
Maintain comprehensive drawing lists (P&IDs, PFDs, Architectural, MEP drawings)
Ensure accuracy and adherence to CAD standards
Coordinate drawing files and electronic transmittals
Manage electronic project file systems
Perform site surveys and as-built documentation
Standards & Quality
Maintain global CAD standards
Ensure GMP-compliant documentation
Maintain audit-ready master drawings for regulatory review
Verify drawing updates and chart compliance
Manage workflows in document management systems (GEDMS , ZVS)
Project Support
Participate in construction/renovation projects
Coordinate with project managers on CAD requirements
Review contractor drawings for compliance to Sanofi standards
Support change control, deviation, and CAPA processes
Provide urgent support for projects or regulatory affairs
Collaboration & Communication
Work with cross-functional teams (engineers, project managers, quality)
Provide guidance on CAD systems and standards
Support regulatory inspections and audits
Respond to work requests (DT/DICT)
Act as single point of contact for drawing-related queries
Continuous Improvement
Identify opportunities to improve CAD processes
Support digitalization initiatives (3D modelling, BIM, CAFM)
Contribute to alignment with corporate standards
Participate in internal/external committees on building planning
Additional Senior Level responsibilities
Coordinate weekly CAD needs and resource allocation
Distribute and track CAD work among team members
Act as Primary System Owner (PSO) for CAD/CAFM systems
Provide training to staff and contractors
Regular reporting on deliverables and issues
Experience
About you
5-6 years in 2D drafting & 3D modelling in Pharma industries.
Exposure to technical drawings (P&IDs, architectural plans, HVAC systems)
Experience with document management systems
5-6 years in regulated industries (food, medical devices, aerospace)
Understanding of quality systems and compliance
Experience with change control processes, GMP experience, regulatory documentation
Soft Skills
Effective time management
Clear verbal and written communication
Strong attention to detail
Collaborative team player
Independent and systematic working style
Results and solution-oriented approach
Customer focus
Willingness to accept responsibility
Technical Skills
AutoCAD/AutoCAD MEP drafting proficiency
Knowledge of drafting techniques and MEP engineering terminology
Experience with electronic drawing management systems
Understanding of GMP documentation requirements
Site verification and as-built documentation skills
Experience in GMP/pharmaceutical facility environment
3D CAD design experience (Revit, 3D modeling, ACC Cloud)
Specific experience in piping or process design
Experience with Meridian BlueCielo, GEDMS , or similar systems
Knowledge of BIM and CAFM systems
Education: (not mandatory)
High School Diploma + 3-5 years CAD experience OR Associate's Degree + 1-3 years
Or Mid level (LL-4): High School Diploma + 5-7 years CAD experience OR Associate's Degree + 3-5 years
Languages
English (written and spoken) - required
Additional languages based on location (French/German)
Pursue Progress, discover Extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com
Work arrangement
No
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