Production Tech - Syringes

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.

Production Tech - Syringes

Swiftwater, PA

• THIS IS A ROTATING 3RD SHIFT POSITION.

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

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.

• 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…