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Sanofi Group Production Technician - Vaccine in Swiftwater, Pennsylvania

This is a 3rd shift position.

Performs production in accordance with volume fluctuation, business need, and effective procedures. Responsible for Manufacturing activities in assigned area. Ensures all materials required for production are available prior to need. Completes sampling and corresponding documentation as required. Completes move tickets and picklists in an accurate and timely manner to ensure accurate inventory. Participates in all aspects of inventory management (SAP, cycle counting, ordering, etc.). Identifies all production issues and relays them to the leadership team. Works to prepare assigned areas for the oncoming shifts. Completes tasks and corresponding documentation as required by cGMP. Works with Senior Technicians and Managers to ensure a smooth operation. Works to become trained in all assigned training modules. Trains and orients new team members (at any level) as assigned

Follows effective procedures to ensure the production of a safe and efficacious product. Works to understand cGMP’s. Identifies areas of deficiency to the leadership team and offers potential suggestions for improvements. Participates in both deviation investigations when appropriate and implementation plans to ensure a quality product. Works with the leadership team to complete deviation investigations and root cause analysis. Works to complete quality documentation (BPR’s, logbooks, etc) accurately in a timely manner. CFR (code of federal regulations) / PAI inspection readiness. FDA audit understanding and awareness.

Participates in team meetings. Actively communicates improvement ideas, issues, concerns, etc to team members. Participates in cross functional teams where necessary to complete projects in an effective and timely manner.

Completes picklists and move tickets for all tasks completed on any given day. This may require inputting data into SAP, along with entering work orders and reagent orders. Ensures proper process area operation by pre and post run set up and maintenance of lab and equipment. Recommends changes to BPRs, SOPS and SWIs when warranted. Write and edit documents under supervision. Seeks out cross training in other areas whenever possible. Responsible for assisting in writing and assisting incident investigations, CAPA's, change controls, along with assisting the higher tech levels and Principle Investigators with projects.

All other duties as assigned

Like all production positions at the Company, this position may be required to flex to another department or location within the Biologics platform due to business needs. We will attempt to provide as much advance notice as possible if any such change is needed.

  • HS diploma or equiv and 2+ years in cGMP or Pharmaceutical experience

  • Associates with 1 + yrs in cGMP or Pharmaceutical experience

  • Bachelors with 0 + yrs in cGMP or Pharmaceutical experience

  • Prior or related cGMP or Pharmaceutical experience recommended

  • Requires good mechanical skills, computer skills and is detail oriented. Must have basic mechanical aptitude, computer skills, good comprehension skills, retention skills, troubleshooting and manual dexterity.

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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