Aseptic Production Technician

Location:

Swiftwater, PA

Shift: 2nd shift

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.

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 in accordance with volume fluctuation, business need, and effective procedures.
• 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.
• May serve as processing room leads and strive to become experts in their assigned areas.
• Completes at least one developmental classes annually focused on one of the four core competencies.
• Completes at least one developmental class outside of the core competencies annually.
• 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.
• Actively 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.
• 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.
• 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 Principle Investigators with projects.
• All other duties as assigned.

• Requires good mechanical skills,…