Aseptic Production Technician

About the role

• Job title: Aseptic Production Technician
• Location: Swiftwater, PA
• Shift: 2nd shift

About the job

Join a global network that powers how Sanofi delivers - seamlessly, purposefully, and at scale. In Manufacturing & Supply, you'll help reimagine how life-changing treatments reach people everywhere, faster.

Main responsibilities

• 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.

Qualifications

• 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.
• Prior or related cGMP or Pharmaceutical experience recommended
• HS diploma or equivalent and 1+ years in cGMP or Pharmaceutical or any manufacturing experience
• Associate's degree with 6+ months in cGMP or Pharmaceutical or any manufacturing experience
• Bachelor's degree with or without cGMP or Pharmaceutical or any manufacturing experience
• Proficiency in at least but not limited to three areas of operations or product line.
• Must be proficient in at least one of the following areas: Utility Sampling, equipment prep, tank movement OR Must be a qualified trainer in vial wash or debag and SAP
• Must have knowledge and access to systems (SAP, Master, SCADA, RT Reports, Labware) OR Must have knowledge and access to systems (SAP, HMI).
• All other duties as assigned.

Why Choose Us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
• #GD-SP
• #LI-SP
• #LI-Onsite
• #vhd
• Pursue progress, discover extraordinary

Additional information

Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.

Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 () or

Pay and benefits

The salary range for this position is: $20.32 - $27.09

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.