Production Tech - Syringes
Listed on 2026-09-12
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Manufacturing / Production
Manufacturing & Industrial Operations, Pharmaceutical Manufacturing, Occupational Health & Safety
Job title:
Production Tech - Syringes
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 www.sanofipasteur.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.
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.
- HS 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
- Must successfully pass Ase
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