About the role
Department Description:
The MA Bio-Campus is home to Sanofi’s digital facility which won ISPE’s Facility of the Future and Facility of the Year 2020. As such, the Manufacturing Systems & Automation group in is responsible for executing Sanofi’s Digital Strategy to deliver innovative solutions. Focused on Digital 4.0, this group is involved in delivering digital solutions for large capital projects as well as continuous improvement and optimizing existing solutions. The group is responsible for design, implementation, support, and maintenance of digital systems aligned with site and company goals. group is responsible for maintaining stable, qualified, and highly available computing infrastructure and digital software applications. This encompasses work processes that originate with the identification of a new or revised digital systems, the design, installation, verification and validation of the system, the maintenance of the system in its commissioned/qualified/validated state and the retirement of the system at the end of its life.
About Sanofi:
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve lives.
Position Overview with Key Responsibilities:
Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs. This position is responsible for providing automation expertise for small to medium projects. These projects include continuous improvement and retrofit. This person will troubleshoot and support delivery of future enhancements for automation related systems. The Automation Engineer II will be responsible for maintaining and providing technical support, ensuring availability of the automation systems for multiple manufacturing facilities.
Additional Responsibilities include:
Leadership:
- Providing leadership and direction to junior team members while embodying the principles of the Sanofi Global Leadership Model
- Ensuring timely issue escalation to senior management and cross-functional support teams
- Partnering with support teams i.e., Manufacturing, Quality, etc to ensure deliverables are completed to meet to production schedules
Automation:
- Provide technical solutions to a wide range of process automation related design challenges. Solutions are imaginative, thorough, practical, and consistent with organization objectives
- Responsible for ensuring process equipment automation are available to support operations schedule requirements
- Managing small departmental projects and ensuring that the appropriate controls, approvals, and validation requirements are implemented
- Integrate systems and data from a variety of skidded systems, analytical equipment, and process/building control systems
- Developing robust solutions that have minimal downtime and ensure data integrity
- Contribute to the development of automation standards
Training /Deviations /Compliance/Safety:
- Complying with Sanofi requirements for training
- Ensuring Inspection Readiness of assigned areas
- Overseeing completion of investigations and deviations
- Ensuring all assigned deviations and CAPA’s are closed in a timely manner
- Ensuring that Automation documentation is compliant and inspection ready
- Participating in inspections conducted by external regulators
- Complying with requirements from Genzyme’s Safety Program including Health and Safety regulations and OSHA requirements
Continuous Improvement:
- Working collaboratively with inter-department and cross-functional teams to lead necessary changes in a timely and productive manner
- Partnering with Manufacturing to troubleshoot and drive resolution of process issues and proactively driving projects to improve manufacturing process
- Partnering with Operational Excellence to drive process improvements through Kaizens, Kanban, 5S and VSM
About You
Basic Qualifications:
- Bachelor’s degree in engineering, Science or related technological field and 2+ years of experience in the automation field preferably in the life sciences
- Master’s degree with 1+ years of experience in the automation field preferably in the life sciences field
- Direct experience with regulated environments (i.e. cGMP, OSHA, EPA)
Preferred Qualifications:
- Experience with DeltaV automation
- Experience with multiple computerized systems (Ignition, Werum PAS-X, PI, etc.)
- Experience with SCADA/PLC systems such as Rockwell Factory Talk/RSLogix, Honeywell
- Understanding of network infrastructure
- Experience with systems/network/validation, preferable in the chemical, pharmaceutical, foods, or other process industries is preferred
- Electrical Engineer or Chemical Engineer
- Experienced in establishment of safe practices in a cGMP environment.
- Understanding of virtual environments, VMWare, Hyper-V
- Proficient working with computer programs/applications such as Windows, VBA, MS Word, Excel, Access, etc.
- Strong organizational skills
- Self-motivated with the ability to work independently and be accountable
- Proven technical and analytical skills to quickly resolve automation system issues
Special Working Conditions:
- Required manufacturing operations support on a rotating “on call” 24/7 basis
- Requires working in an industrial manufacturing environment including gowning
Why choose us?
- Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
- Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale.
- Transform lives worldwide by delivering life-changing treatments anywhere, anytime.
- Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.