The Framingham 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 Digital Operations Technology group in Framingham 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 Digital Operations Technology group is responsible for design, implementation, support, and maintenance of digital systems aligned with site and company goals. The Digital Operations Technology 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.
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. This person will design, architect, troubleshoot, and deliver future enhancements for Automation related systems. The person will be responsible for maintaining and providing technical support, ensuring availability of the automation systems for multiple manufacturing facilities.
In addition, this position is responsible for being a systems engineer and a technical system owner for shop floor automation systems. System management, maintenance, upgrades, and lifecycle planning are key responsibilities of this position.
Additional Responsibilities include:
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 to medium 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.
Support 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.
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.
Bachelor’s degree in Engineering, Science or related technological field and 5 to 7 years of experience
Master’s with 3 to 5 years of relevant work experience
Experience with DeltaV a minimum of 3 years
Direct experience with regulated environments (i.e. cGMP, OSHA, EPA)
Demonstrated knowledge of bus technologies and Instrumentation
Demonstrated knowledge of validation requirements for control systems in CGMP and/or ASTM environments
Experience with multiple computerized systems (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 XP, Windows 7, 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:
As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. This position will require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.