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Professional Continuous Improvement

Swiftwater, Pennsylvania



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This position takes a role in identifying, gaining consensus and resolving issues of safety, compliance and efficiency that impact the FFIP (Formulation, Filling, Inspection and Packaging) Platform.  The role contributes as a member of cross-functional teams to support the FFIP platform and functions as an interface between the FFIP platform and the Technical Community (especially Engineering/Maintenance and Manufacturing Technology). 

Location: Swiftwater, PA

As part of the organization, this role does the following:

  • Individual contributor role that is member of cross-functional teams that provide support for the FFaST (Focus Factory and Support Team) efforts for the Factory. 
  • Provides Continuous Improvement for the Factory.
  • Provides project support for cross functional teams.
  • Provides Factory interface for working through project issues.
  • Provides technical support for the factory.

Key Accountability:

  • Provides Continuous Improvement support for the factory; These are small/medium individual projects to improve OEE, Deviations, Yield, etc. 
  • This organization will provide project support to accomplish these efforts. 
  • These projects may be FFaST projects or managing Change Controls and CAPA’s for the production unit.
  • This group will be interface for technical transfers, engineering projects and similar activities and provide support for the projects, especially for time intensive and major projects.
  • Provides technical support for component qualification, OEE improvement, and general factory improvements and general technical support for the Factory.
  • Ensure efficient and effective operation by creating a proactive environment, developing & monitoring metrics, and communicating with both team members and support functions about operations performance. 
  • Utilizing the "+QDCI" Visual Management Systems and Working with the FFIP Management Committee to drive improvements in key metrics.
  • Ensure compliance with all regulatory requirements and good documentation practices are followed to provide a safe, quality, and effective product.

Basic Qualifications:

  • BS required in Life Sciences or Engineering. 
  • 0-2 years; industry experience in large scale biotech, pharmaceutical, manufacturing, maintenance, engineering or analytical & process development areas. 

Other Skills:

  • Must have excellent written and verbal communication skills, as well as the ability to actively, and cooperatively work with cross functional teams.

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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