Aseptic Filling Operator — Pharma Manufacturing

Guerbet; Raleigh (NC); On-site; USD 42,000 - 65,000; Full time

Job summary

Guerbet is seeking a Filling Operator to produce pharmaceutical products in an aseptic environment at our Raleigh site. You will operate filling equipment, monitor batch operations, and ensure quality and safety in line with cGMP and GDP.

The role requires 1–2 years in pharmaceutical production, a high school diploma or equivalent, and solid aseptic techniques. You will complete batch records, maintain sterile conditions, and collaborate with engineering and validation teams.

Qualifications

• High School diploma, GED, or equivalent required.
• 1–2 years’ experience as a Production Operator in pharmaceutical manufacturing preferred.
• Knowledge of basic computer skills and Microsoft Office.
• Skilled in handling basic hand tools for routine adjustments.
• Strong knowledge of aseptic processing, cleanroom standards, and sterile techniques.

Responsibilities

• Operate and monitor filling equipment for efficient production.
• Monitor equipment during operation to ensure product quality.
• Perform cleaning and sanitization of aseptic areas using approved disinfectants.
• Maintain aseptic techniques during gowning and material transfer.
• Complete batch records and deviation reports in line with cGMP.
• Report contamination events or deviations promptly.

Skills

Aseptic processing

Cleanroom standards

Sterile techniques

Basic computer skills

Hand tools usage

Attention to detail

Teamwork

Education

High School diploma, GED, or equivalent

Tools

Microsoft Office

Electric pallet jack

Job description

Guerbet is seeking a Filling Operator to produce pharmaceutical products in an aseptic environment at our Raleigh site. You will operate filling equipment, monitor batch operations, and ensure quality and safety in line with cGMP and GDP.

The role requires 1–2 years in pharmaceutical production, a high school diploma or equivalent, and solid aseptic techniques. You will complete batch records, maintain sterile conditions, and collaborate with engineering and validation teams.