Manager, FFIP Continuous Improvement - Vaccines
Listed on 2026-06-26
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Manufacturing / Production
Quality Engineering -
Engineering
Quality Engineering
Job Title
:
Manager, FFIP Continuous Improvement - Vaccines
- Location: Swiftwater, PA
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). As part of the organization, this role ensures the following:
- Individual contributor role that is member of cross‑functional teams that provide support for the PCU (Process‑Centric Unit) 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.
- Provides Continuous Improvement support for the factory, including small to medium projects to improve OEE, Deviations, Yield, etc. Projects may involve Continuous Improvement or managing Change Controls and CAPA’s for the production unit.
- Provides project support interfaced for technical transfers, engineering projects and similar activities, especially for time‑intensive and major projects.
- Provides technical support for component qualification, OEE improvement, and general factory improvements.
- Ensures efficient and effective operation by creating a proactive environment, developing and monitoring metrics, and communicating with team members and support functions about operations performance using the Visual Management Systems and working with the FFIP Management Committee.
- Ensures compliance with all regulatory requirements and good documentation practices to provide a safe, quality, and effective product.
- Bachelor's Degree in Life Sciences or Engineering, or related fields.
- 2+ years of large‑scale biotech or pharmaceutical manufacturing, maintenance, engineering, analytical, and process development experience.
- Excellent written and verbal communication skills and 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 status, domestic partnership, civil union status, sex, gender, gender identity, expression, sexual orientation, disability, veteran or military status, liability for military status, domestic violence victim status, atypical cellular or blood trait, genetic information, or any other characteristic protected by law.
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in company employee benefit programs, and additional benefits information is available.
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