Visual Inspection Engineer

Intellectt INC; New York (NY); On-site; USD 83,000 - 92,000; Full time

Job summary

Intellectt INC is seeking a Visual Inspection Engineer for on-site work in Rensselaer, NY to optimize vision systems used in pharmaceutical manufacturing, with a strong emphasis on camera tuning and defect detection.

The contractor will support process validation, qualification activities, lifecycle documentation, and general project engineering for two new process lines during commissioning, in a GMP setting, with independent, proactive collaboration across teams.

Qualifications

• 7+ years of experience with automated vision inspection systems in pharma manufacturing.
• Hands-on camera tuning and optimization of inspection equipment.
• Experience with Seidenader, CoBER/CorBER, SVI, or similar systems.
• Strong GMP, process validation, and lifecycle documentation experience.
• Ability to troubleshoot vision systems and reduce false positives.
• Excellent independent work and communication skills.

Responsibilities

• Sit onsite 5x/week in Rensselaer, NY to optimize vision inspection equipment.
• Support process validation, qualification activities, and lifecycle documentation.
• Assist with commissioning of two new process lines across stages.
• Improve inspection accuracy and reduce rejects across defect types.
• Coordinate with technical and non-technical stakeholders in GMP environment.

Skills

Vision systems

Camera tuning

GMP experience

Documentation

Troubleshooting

Tools

Seidenader

CoBER/CorBER

SVI

Job description

Job Title: Visual Inspection Engineer

Location: Rensselaer, NY

Duration: 12 months

Pay Rate:$60/hr- $67/hr on W2

Must Haves

• 7+ years of experience working with automated vision inspection systems in a pharmaceutical manufacturing environment
• Hands-on experience tuning and optimizing camera-based inspection equipment
• Experience with Seidenader, CoBER/CorBER, SVI, or similar automated vision systems
• Strong background supporting process validation, qualification, and GMP-regulated manufacturing operations
• Experience creating and executing lifecycle documentation (SLC) and engineering documentation
• Ability to troubleshoot vision systems and reduce false positives/reject rates on automated inspection equipment
• Strong communication skills and ability to operate independently

Plusses

• Principal or Staff-level engineering expertise
• Ability to bridge technical and non-technical stakeholders
• Experience supporting new equipment start-ups and qualification activities
• Science or Engineering degree Background in project engineering within pharmaceutical manufacturing

Day to Day

Client is seeking a Vision Systems Engineer to sit onsite 5x/week to support one of our largest pharmaceutical clients onsite in Rensselaer, NY. This individual will be responsible for optimizing and tuning automated vision inspection equipment used in manufacturing operations, with a heavy focus on camera tuning and inspection system performance. This individual will also support process validation, qualification activities, lifecycle documentation, and general project engineering efforts related to newly installed manufacturing equipment, specifically across 2 new process lines in different phases of the commissioning process. This engineer will also support process validation, qualification, lifecycle documentation, and general project engineering efforts related to newly installed manufacturing equipment, specifically across 2 new process lines in different phases of the commissioning process. This engineer will have strong expertise with automated inspection platforms such as Seidenader, CoBER/CorBER, SVI, or similar technologies and will be responsible for improving inspection accuracy, reducing false positives, and ensuring equipment is properly configured across all defect types. This engineer will also support process validation, qualification activities, lifecycle documentation, and general project engineering efforts related to newly installed manufacturing equipment, specifically across 2 new process lines in different phases of the commissioning process. This engineer will also have proven vision systems expertise over traditional project engineering backgrounds and the ability to operate autonomously, communicate effectively across technical and non-technical teams, and make an immediate impact within a GMP-regulated pharmaceutical environment.

Benefits

This a contract position does not include employer-provided benefits.

Equal Opportunity Employer:

We are an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Background Check:

Background checks may be conducted in accordance with applicable law.

Work Authorization:

Applicants must be authorized to work in the United States