Evening Quality Control Inspector - Pharma | OT Eligible

VSSI Staffing Services; Town of Texas (WI); On-site; USD 28,000 - 32,000; Full time

Job summary

VSSI Staffing Services is hiring a QC Inspector in Wisconsin. The role focuses on testing, data review, and investigations in compliance with cGMPs and SOPs. The position executes product analyses, adheres to SOPs, and ensures proper documentation and equipment readiness for production.

The candidate will support calibration, sanitation verification, and sample management to sustain quality standards. The role requires a degree or equivalent experience, 2–4 years in pharma or related fields, and

Qualifications

• Bachelor’s degree in related field or equivalent experience.
• 2–4 years related experience or equivalent.
• Knowledge of pharmaceutical manufacturing processes, GMPs, and validation.
• Ability to develop clear, concise, timely reports (oral and written).
• Experience in laboratory environment, equipment, and safety procedures.
• Experience in R&D including statistics understanding.

Responsibilities

• Analyze products per cGMP and SOPs.
• Follow work instructions and SOPs.
• Inspect production areas, processes, and finished goods.
• Document data in forms, logs, and inventories.
• Calibrate and maintain equipment per GMP and SOPs.
• Monitor cleanliness and report issues.
• Read and follow SOPs and GMPs.
• Swab and verify equipment cleanliness with ATP testing.
• Prepare and drop off customer samples for shipment.
• Maintain retain samples in Excel workflow.
• Review BOM and production processes before production.
• Follow safety regulations.
• Perform other duties as assigned.

Skills

Analytical thinking

Attention to detail

Oral communication

Written communication

Teamwork

Education

Bachelor's degree or equivalent

Tools

Laboratory equipment

Job description

VSSI Staffing Services is hiring a QC Inspector in Wisconsin. The role focuses on testing, data review, and investigations in compliance with cGMPs and SOPs. The position executes product analyses, adheres to SOPs, and ensures proper documentation and equipment readiness for production.

The candidate will support calibration, sanitation verification, and sample management to sustain quality standards. The role requires a degree or equivalent experience, 2–4 years in pharma or related fields, and