Production Technician

## Production Technician Apply locations:
Swiftwater, PAtime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
July 10, 2026 (21 days left to apply) job requisition :
R2859149
*
* Job title:

** Production Technician
*
* Location:

** Swiftwater, PA
** THIS IS A ROTATING 3RD SHIFT POSITION.
**** About the job
** Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and  Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

Sanofi Pasteur, the vaccines division of Sanofi, provides more than 1 billion doses of vaccine each year, making it possible to immunize more than 500 million people across the globe. A world leader in the vaccine industry, Sanofi Pasteur offers a broad range of vaccines protecting against 20 infectious diseases. The company's heritage, to create vaccines that protect life, dates back more than a century.

Sanofi Pasteur is the largest company entirely dedicated to vaccines. Every day, the company invests more than EUR 1 million in research and development. For more information, please visit:  or (Use the "Apply for this Job" box below)..us
** About Sanofi
** We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
*
* Main Responsibilities:

*** Performs production activities in accordance with volume fluctuation, business need, and effective procedures.
* Works to support production units by consistently providing required materials in a timely manner.
* Ensures all materials required for production are available prior to need.
* Identifies production issues and relays them to the leadership team.
* Ensures all required paperwork is complete, accurate and done in a timely manner to ensure accurate inventory.
* Completes tasks and corresponding documentation as required by cGMP.
* Works to prepare assigned areas for the oncoming shifts.
* Completes at least one developmental class annually focused on one of the four core competencies.
* Works to become trained in all assigned training modules.
* Trains and orients new team members (at any level) as assigned.
* Follows all procedures put into effect to ensure your safety as well as the safety of others.
* Participates in monthly safety meetings.
* Report all safety issues, concerns, incidents and near misses to the team leadership.
* Participates in safety walkthroughs coordinated by the department’s safety team.
* Provides input for potential safety issues as well as contributing ideas for corrective and preventative actions.
* 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.
* May participate in completion of quality documentation (BPR's, logbooks, etc.).FDA audit understanding and awareness.
* Participates in team meetings.  Actively communicates improvement ideas, issues, concerns, etc to team.
* Participates in cross functional teams where necessary to complete projects in an effective and timely manner.
* Lead Operator, 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 were 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 Principal Investigators with projects. All other duties as assigned.
** About You
**** Basic…