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Sanofi

Global pharma company; vaccines and R&D

Automation Engineer

Controls & Automation EngineeringConfirmed live in the last 24 hours
Full-timeSwiftwater, PA, USA$75k - $108.3kIn-person

About the Job

Requirements

  • At least 2 years of direct experience in automation systems and automation support within biopharma or related industries; this is described as preferred.
  • Knowledge of distributed control systems such as DeltaV, supervisory control and data acquisition systems such as Aveva, programmable logic controllers, and related automation technologies in manufacturing.
  • Knowledge of machine connectivity and data acquisition from programmable logic controllers into higher-level applications such as historians and enterprise resource planning systems, using technologies such as OPC; this is described as preferred.
  • Ability to collaborate effectively with cross-functional teams.
  • Problem-solving abilities.
  • Effective communication skills for engaging diverse stakeholders across projects.
  • Bachelor’s degree in engineering, Electrical, Chemical, Mechanical, Automation, Computer Science, Biotechnology, Computer Sciences, or an applicable technical field related to engineering in the biopharma sector; relevant work experience may substitute for the college degree.
  • Proficiency in written and spoken English.

Responsibilities

  • Support implementation of changes to automation systems, update design documents, execute testing, troubleshoot events, and participate in site automation on-call support.
  • Provide subject matter expert support for automated process control systems used in licensed manufacturing, including dedicated clean utilities, for the assigned building.
  • Serve as the Manufacturing Systems & Automation Site Support interface with Operations, QA Compliance, Information Systems, Engineering, Maintenance, and site automation support technicians.
  • Provide hands-on support for automated systems in manufacturing, including building automation systems; troubleshoot automated process equipment and process systems; coordinate contractors; execute site change controls; aid in investigating process deviations; and provide expertise for process evaluation and product improvements to improve quality and yields.
  • Implement site automation standard procedures and Global Engineering Practices.
  • Ensure seamless integration of automation systems with digital applications supporting production, quality control, and data management.
  • Ensure compliance with GMP and regulatory standards, including development of user, functional, and detailed specifications, test protocols, and system validation.
  • Work with clients to understand their needs and develop tailored strategies through site assessments.
  • Identify and proactively manage risks, and ensure GMP compliance to minimize disruptions to timelines and costs.
  • Develop and deliver specialized training materials for staff to support proper operation and maintenance of automated systems, and provide ongoing post-implementation support.
  • Collaborate with Manufacturing, Supply Chain, Quality, Facilities, and Tech Transfer departments to capture and document detailed requirements.
  • Develop standards and best practices for development and validation activities.
  • Lead cross-functional teams through design reviews and user acceptance testing during development changes and validation.
  • Participate in facility operational meetings to ensure facility reporting needs are met.
  • Oversee daily monitoring, troubleshooting, and support of programmable logic controllers, supervisory control and data acquisition systems, distributed control systems, and other control systems to ensure continuous production with minimal downtime and maximum efficiency.
  • Identify, propose, and implement process and system improvements to enhance automation performance, reduce costs, and improve manufacturing flexibility.
  • Work with engineering, production, quality, IT, and other cross-functional teams to align automation systems with production goals and regulatory requirements.
  • Ensure automation activities comply with GMP, safety standards, and other relevant regulations; lead risk-management efforts for automation systems and proactively address compliance issues.
  • Provide off-shift on-call support on a rotating schedule for manufacturing operations.

Desired Qualifications

  • At least 2 years of direct experience in automation systems and automation support within biopharma or related industries.
  • Knowledge of machine connectivity and data acquisition from programmable logic controllers into higher-level applications such as historians and enterprise resource planning systems, using current technologies such as OPC.

About the Company

Sanofi

Global pharma company; vaccines and R&D

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company size
10,001+
Company stage
IPO
Headquarters
Paris, France
Founded
1973

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