- *Job title:** Senior Drawer
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:**
1\. 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
2\. 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)
3\. 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
4\. 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
5\. 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
6\. 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
- 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