Sterile Visual Inspection Technician I – 2nd Shift

Alcami Corporation; South Carolina; On-site; USD 25,000 - 30,000; Full time

Job summary

Alcami Corporation is seeking a Visual Inspection Technician I to perform quality inspection of sterile injectable products for commercial and clinical trial use. The role requires following SOPs and cGMPs, handling PPE gowning, and documenting activities in real time on controlled systems.

The position is 2nd shift, on-site, with responsibilities including debris and defect inspection, documentation, and packaging readiness. Prior regulated environment experience is preferred.

Qualifications

• High school diploma or GED required; Associate degree preferred.
• Entry level with 1+ years of relevant experience strongly preferred OR BioWork certification.
• Experience in regulated environments with visual inspection is applicable.
• cGMP or prior work experience in a regulated environment preferred.
• Pharmaceutical or CDMO experience preferred.

Responsibilities

• Follows SOPs and cGMPs to perform duties and tasks.
• Ensures timely completion and compliance with training requirements.
• Conducts visual inspection of sterile liquids per guidelines.
• Identify debris, air lines, and defects in sterile liquids.
• Documents activities in real time on controlled documentation.
• Performs component counting and basic math calculations.
• Performs cleaning of rooms, tools, and equipment.
• Performs specific visual inspections per SOPs.
• Ensures product meets appearance specs before packaging.
• Performs bulk packaging for product vials.
• Operates material handling equipment.
• May work outside schedule including weekends.
• Other duties as assigned.

Skills

Visual inspection

Attention to detail

Quality control

Basic math

Education

High school diploma or GED

Associate degree preferred

Tools

BioWork certification

Job description

Alcami Corporation is seeking a Visual Inspection Technician I to perform quality inspection of sterile injectable products for commercial and clinical trial use. The role requires following SOPs and cGMPs, handling PPE gowning, and documenting activities in real time on controlled systems.

The position is 2nd shift, on-site, with responsibilities including debris and defect inspection, documentation, and packaging readiness. Prior regulated environment experience is preferred.