Aseptic Production Technician (2nd Shift) - Growth & GMP Expert

Sanofi; Swiftwater (Monroe County); On-site; USD 32,000 - 47,000; Full time

Job summary

Sanofi Pasteur SA in Swiftwater, PA is seeking an Aseptic Production Technician for the 2nd shift to support manufacturing operations. You will perform production tasks, ensure material readiness, and help maintain cGMP-compliant processes within a global biopharma setting.

The role emphasizes quality documentation, safety, teamwork, and ongoing training to develop expertise across several production areas and systems.

Qualifications

• 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 three areas of operations or product line.

Responsibilities

• Performs production in accordance with volume fluctuation and procedures.
• Ensures materials required for production are available and completes sampling/docs.
• Participates in inventory management (SAP, cycle counting, ordering).
• Identifies production issues and relays to leadership.
• Prepares areas for shifts and completes required documentation.
• Trains and orients new team members and participates in safety meetings.
• Participates in deviation investigations and root cause analysis.
• Writes and edits quality documentation and participates in CFR/PAI readiness.

Skills

Mechanical skills

Detail oriented

Computer skills

Troubleshooting

Manual dexterity

Retention skills

Comprehension skills

Education

HS diploma or equivalent

Associate's degree

Bachelor's degree

Tools

SAP

Master

SCADA

RT Reports

Labware

HMI

Job description

Sanofi Pasteur SA in Swiftwater, PA is seeking an Aseptic Production Technician for the 2nd shift to support manufacturing operations. You will perform production tasks, ensure material readiness, and help maintain cGMP-compliant processes within a global biopharma setting.

The role emphasizes quality documentation, safety, teamwork, and ongoing training to develop expertise across several production areas and systems.