Quality Visual Inspection

Lancesoft; Fargo (ND); Presencial; USD 22 000 - 30 000; Tempo integral

Resumo da oferta

Lancesoft is seeking a GMP Visual Inspector in Fargo, ND, for 0-6+ months on a full-time basis. The role requires performing 100% manual visual inspection of filled and sealed drug product vials in a controlled environment, focusing on accuracy and documentation.

No prior visual inspection experience is required; structured training is provided. Candidates should have a high school diploma or GED, good eyesight, and reliable attendance for first or second shift duties.

Qualificações

• High school diploma or GED required; life sciences degree preferred.
• Ability to read and understand written procedures and complete clear records.
• Detail-oriented with good eyesight and steady hands for small-vial inspection.
• Reliable attendance and ability to work first or second shift.
• Comfort with documenting results in English and following GDP requirements.

Responsabilidades

• Perform 100% manual visual inspection of filled and sealed vials under controlled lighting.
• Identify visible defects and document results, segregating rejects for further evaluation.
• Maintain qualification and complete required GMP, GDP, safety, and technique training.
• Support reconciliation of inspected and accepted units and record-keeping.
• Follow eye breaks, gowning, and area-control procedures during inspection.

Conhecimentos

Attention to detail

Reading procedures

English documentation

Math basics

Attendance reliability

Formação académica

High school diploma or GED

Bachelor's degree in life sciences preferred

Descrição da oferta de emprego

Duration: 0-6+ Months Shift: 1st Shift (Mon - Fri)

Job Description: The GMP Visual Inspector performs 100% manual visual inspection of filled and sealed drug product vials. Using a controlled inspection booth, standardized lighting, and approved techniques, the inspector evaluates each vial for visible particulate matter and container, closure, fill, and cosmetic defects. Nonconforming units are removed, uncertain conditions are escalated, and inspection results are documented when the work is performed. This is a dedicated, full-time inspection role. Previous pharmaceutical or visual inspection experience is not required. Success depends on patience, concentration, consistency, visual attention, and willingness to follow a defined method every time. Structured training and qualifications are provided. What to Expect: This is focused, repetitive, precision work. Inspectors spend much of the shift examining small glass vials under controlled lighting, with required eye breaks built into the process. Some training products are clear and straightforward. Most will be opaque, colored, or visually challenging. Accuracy is more important than speed. Work in a quiet, controlled environment where distractions are minimized. Use the same approved inspection technique consistently throughout the shift. Reject defects and route uncertain conditions for further evaluation rather than guessing. Handle high-value drug product carefully and maintain accurate reconciliation and documentation.

Key Responsibilities:

• Complete required GMP, GDP, safety, procedure, defect-recognition, and inspection-technique training.
• Successfully complete initial qualification before independently inspecting GMP product and maintain active qualification status.
• Perform 100% manual visual inspection of assigned filled and sealed vials using approved lighting, backgrounds, handling technique, and inspection timing.
• Identify and document visible particles, fibers, fill-volume concerns, container or closure defects, scratches, scuffs, discoloration, and other defined defects.
• Segregate rejected units and units requiring further evaluation while maintaining clear material status and chain of custody.
• Record inspection results accurately and contemporaneously in accordance with GDP requirements.
• Follow required inspection intervals, eye breaks, area controls, gowning, hygiene, and product-handling requirements.
• Support reconciliation of inspected, accepted, rejected, and further-evaluation units.
• Participate in refresher training, requalification, defect-kit activities, and continuing inspection practice as assigned.
• When inspection demand is lower, support approved Drug Product activities such as training, area readiness, defect-kit preparation, inventory, documentation support, or continuous improvement within the employee's training and authorization.

Minimum Qualifications:

• High school diploma or GED.
• Bachelor's of Science in life science preferred.
• Ability to read and understand written procedures, follow step-by-step instructions, and complete clear, accurate records in English.
• Basic math skills sufficient for counts, reconciliation, and simple calculations.
• Ability to maintain sustained attention during repetitive, detail-oriented work.
• Reliable attendance and ability to work the assigned first- or second-shift schedule.
• Good documentation practices Ability to meet role-specific visual requirements, including 20/20 near visual acuity with or without corrective lenses and the ability to distinguish required colors, as confirmed through the applicable eye examination.
• Ability to handle small glass vials safely and perform fine visual and manual work during scheduled inspection periods.

Preferred Qualifications:

• Prior experience is not required. Experience in pharmaceutical, medical-device, laboratory, electronics, precision assembly, quality inspection, manufacturing, or other detail-oriented work may be helpful.