GMP Visual Inspector
Posted:
22 October 2026 (2 days ago)
Application Deadline:
19 January 2027
Vacancies:
1 Vacancy
Job Summary
Duration: 0-12 Months
Shift: First shift is 7:30am - 3:30pm / Second shift is 3:00pm - 1:30am Central time
Job Description:
Position Summary
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 qualification 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.
Key Responsibilities
Minimum Qualifications
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.
Shift: First shift is 7:30am - 3:30pm / Second shift is 3:00pm - 1:30am Central time
Job Description:
Position Summary
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 qualification 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 employees training and authorization.
Minimum Qualifications
- High school diploma or GED.
- 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.
- 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.
Required Experience:
IC
About Company
LanceSoft is a global workforce solutions company connecting businesses with top talent across industries and geographies.