Production Technician

Location: Northern

## Production Technician Apply:
Swiftwater, PA:
Full time:
Posted Today:
End Date:
October 9, 2026 (27 days left to apply):
R2869848
*
* Job Title:

** Production Technician
*
* Location:

** Swiftwater, PA
** Shif
* * t: 3rd shift
** About the Job
** The Production Technician – Vaccine is responsible for supporting all aspects of the visual inspection production process in compliance with cGMP standards. This role requires strong mechanical aptitude, attention to detail, and a commitment to quality, safety, and continuous improvement.
** 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:

*** Responsibilities include, but are not limited to:
*** Safety
* ** Participates in monthly safety meetings.
* Reports all safety issues, concerns, incidents, and near misses to team leadership.
* Understands how to work the SRR system.
* Works with the safety and leadership team to provide input on potential safety issues, contribute ideas, and implement all safety initiatives by actively communicating them and helping others understand.
* Works with the safety team to ensure resources required to address safety issues are secured in a timely manner and that effective resolutions are put in place and trained upon.
** Quality
* ** Maintains FDA audit understanding and awareness; ensures processes in assigned areas follow proper procedures at all times.
* Responsible for verifying qualification status prior to performing any task; immediately notifies management if assigned a task for which they are not qualified.
* Identifies and reports any variation from standard operating procedures.
* Participates in variance from SOP and incident investigations as required.
* Ensures completion and review of quality documentation (BRs, logbooks, etc.) accurately and in real-time.
* Ensures strict adherence to ALCOA documentation requirements.
* Follows proper documentation practices as required by cGMP.
* Understands the function of the quality group.
* Writes, edits, and reviews process documentation for completeness.
* Identifies areas of deficiency and offers suggestions for improvements.
** Delivery
* ** Responsible for execution of all required tasks including: zone 1, zone 2, bench inspection, cap check, stopper check, and relief.
* Gains and maintains manual bench inspection qualification; notifies management of failure to qualify or loss of qualification.
* Gains and maintains qualification on all automated inspection processes.
* Gains and maintains qualification in all zone 1 activities.
* Participates in delivery and reconciliation with QC.
* Ensures the completion of sampling and corresponding documentation as required.
* Performs sample delivery on site.
* Ensures all data generation via E  and iSHIFT is performed in real-time.
* Gains initial access and maintains proficiency in E  and iSHIFT.
** Cost
* ** Participates in all aspects of the production process and maintains access to required systems. Examples include:  + E  Data Entry  + iSHIFT (S4

HANA) Transactions  + LIMs Labware (Citrix/WARP)  + Ops Trakker (MIRA2 & MIRA4)  + HMI/Network Access  + Qualipso
* Actively communicates improvement ideas, issues, and concerns to management along with proposing solutions.
* Performs continuous monitoring of reject rates.
* Works to resolve common production issues related to area of work.
** Involvement
* ** Maintains qualification in all assigned training modules.
* Maintains a target of 95–100%…