2nd Shift Aseptic Manufacturing Technician

Sanofi Group; Swiftwater (Monroe County); On-site; USD 28,000 - 37,000; Full time

Job summary

Sanofi is seeking an Aseptic Production Technician for 2nd shift in Swiftwater, PA. You will join a global manufacturing network, ensuring materials readiness, accurate sampling, and compliant documentation while maintaining cGMP standards.

Work alongside senior technicians and managers, train in multiple modules, and contribute to safety, quality, and continuous improvement initiatives. This role offers hands-on production experience in a regulated biopharma environment.

Qualifications

• Good mechanical skills, attention to detail, and basic computer skills.
• Proven troubleshooting abilities and manual dexterity.
• Experience in cGMP or pharmaceutical manufacturing recommended.
• HS diploma or equivalent with 1+ years in cGMP/pharma manufacturing.
• Associate's or Bachelor's degree with related manufacturing exposure.

Responsibilities

• Perform production tasks per procedures and adjust for volume fluctuations.
• Ensure materials are available before production; complete sampling and documentation.
• Manage picklists, SAP entries, and inventory activities.
• Identify production issues and communicate with leadership; support safe operations.
• Train and orient new team members; participate in safety meetings and audits.
• Follow cGMP procedures and maintain quality documentation (BPRs, logbooks).
• Assist with deviation investigations, CAPAs, and change controls.
• Lead operators may input data into SAP and manage work orders.

Skills

Mechanical skills

Computer skills

Attention to detail

Troubleshooting

Manual dexterity

cGMP experience

Education

HS diploma or equivalent

Associate's degree

Bachelor's degree

Tools

SAP

Master

SCADA

RT Reports

Labware

HMI

Job description

Sanofi is seeking an Aseptic Production Technician for 2nd shift in Swiftwater, PA. You will join a global manufacturing network, ensuring materials readiness, accurate sampling, and compliant documentation while maintaining cGMP standards.

Work alongside senior technicians and managers, train in multiple modules, and contribute to safety, quality, and continuous improvement initiatives. This role offers hands-on production experience in a regulated biopharma environment.