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Manager Automation Engineering US, Swiftwater, PA

Manager, Automation Engineering

The Manager Automation Engineering is responsible to manage all automation related issues that affect the day to day operation of the bacterial manufacturing facilities at the Swiftwater site. This position reports to and supports the Deputy Director Automation Site Support, Maintenance, who is ultimately responsible for the efficient, effective and reliable operation of all site-wide automation equipment.?This position will have interactions with Health, Safety and Environment (HSE), Engineering, Site Quality Operations, Information Technology & Solutions, Outside Contractors/Consultants, Industrial Operations and Research & Development departments.

The Automation Manger must exhibit strong customer communication and small project management skills and have knowledge of process control systems and equipment used in biotech/ pharmaceutical manufacturing and utility systems.

This position is expected to manage/execute:

  • Investigate automation issues in a manufacturing environment
  • Direct technicians in troubleshooting equipment
  • Support deviation investigation
  • Site Change Controls for small project execution
  • Implement automation upgrades and improvements
  • Coordinate project validation approach with Site Quality Operations
  • Interactions with operational customers
  • Create and/or update procedures and drawings within the site quality documentation systems
  • The ideal candidate will be familiar with CFRs applicable to the pharmaceutical industry.
  • The focus to create and maintain a safety culture that is proactive and striving for zero injuries is of the utmost importance and an expectation for all employees.
  • Physically located in Swiftwater, PA, Building 49, this position will be supporting all bacterial manufacturing facilities across the Swiftwater site.

Basic Qualifications:

  • B.S. in electrical, mechanical, chemical and/or other applicable engineering field required.
  • Minimum of 1 year experience?working with automated equipment in a pharmaceutical cGMP environment.

Preferred Qualifications:

  • Small project execution experience
  • Experience in the areas of?customer support, operational excellence and troubleshooting.
  • Strong technical background in cGMP manufacturing.

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.

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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.



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