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Sanofi Group ITS Engineer II, Automation in Allston, Massachusetts


The Automation Engineering (AE) Group is responsible for design, implementation, support, and maintenance of automated engineering solutions in support of site goals and objectives. In such, AE is responsible for maintaining a stable, Qualified, and highly available computing infrastructure and implementation and Validated computer systems. This encompasses work processes that originate with the identification of a new or revised system, 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. Additionally, through daily tasks, AE supports current project operations and ensures compliance with regulatory, corporate and site requirements.

This position is responsible for leading and supporting systems management, system maintenance, troubleshooting, and future enhancements. The person will be responsible for maintaining and providing technical support for plant process control equipment, and ensuring execution of production plan across multiple shifts.

Additional Responsibilities include:


  • Providing leadership and direction to support teams while embodying the principles of the Sanofi Global Leadership Model

  • Ensuring timely issue escalation to manufacturing senior management and cross-functional support teams

  • Partnering with support teams i.e., Manufacturing, Quality, etc to ensure adherence to production schedules, while holding direct reports and teams responsible for compliance to all safety and quality regulations.

  • Ensuring that a consistent technical approach for Process Equipment Engineering and Automation is used across Projects.

Problem Solving:

  • Provide technical solutions to a wide range of difficult problems through individual efforts as well as strategic leveraging of outsourced personnel. Solutions are imaginative, thorough, practical, and consistent with organization objectives.

Training /Deviations /Compliance:

  • Complying with Sanofi requirements for training, maintaining training at or above 95% on time

  • Utilizing quality systems to measure, analyze, and improve team performance

  • Partnering with direct and indirect management chain to ensure the following:

  • Ensuring Inspection Readiness of assigned areas

  • Overseeing completion of investigations and deviations.

Partnering with QA to ensure the following:

  • Ensuring all deviations and CAPA’s are closed in a timely manner

  • Providing over sight for deviations and department documentation changes.

  • Ensuring that Process, Equipment and Automation documentation is compliant and inspection ready.

  • Complying with requirements from Genzyme’s Safety Program including Health and Safety regulations and OSHA requirements


  • Responsible for ensuring Process Equipment and Automation are available to support Operations Schedule Adherence requirements.

  • Overseeing departmental projects and ensuring that the appropriate controls, approvals, and validation requirements are implemented

Continuous Improvement:

  • Working collaboratively with inter-department and cross-functional teams to lead necessary changes in a timely and productive manner

  • Identifying opportunities to improve manufacturing processes and practices

  • Ensuring all manufacturing management tools/systems and documentation (SOPs, MBR's, OJTs) is accurate

  • Partnering with Manufacturing to troubleshoot and drive resolution of process issues and proactively driving projects to improve manufacturing process

  • Partnering with Lean Organization to drive business process improvements through Kaizens, Kanban, 5S and VSM.

  • Ensuring that internal customers and suppliers are aligned with the needs and services provided by the Manufacturing Engineering team.

Basic Qualifications

Bachelor’s degree in Engineering, Science or related technological field or 5 years of relevant work experience, or • Master’s or PhD with 3 years of relevant work experience.

• Experience with Rockwell, MES, Siemens and Emerson DeltaV systems.

• 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.

Honeywell or DeltaV experience a MUST HAVE

Preferred Qualifications •

Strong preference for Rockwell Control System Experience

• Experience as a controls engineer, 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.

• Proficient working with computer programs/applications such as Windows, VBA, MS Word, Excel, Access, etc.

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.