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Vision System Engineer

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Onsite

Vision System Engineer

United Pharma

Vision System Engineer

Skills

Process Improvement

1 month ago

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Important information


Contract type:

Freelance / Contract

Location:

New York, NY, USA

Work mode:

Onsite

Published on:

27 September 2026

What they need


We are seeking an experienced Vision System Engineer to support a pharmaceutical manufacturing environment, with a primary focus on machine vision systems and visual inspection equipment . The ideal candidate will have hands-on experience tuning and troubleshooting Körber (formerly Seidenader) Visual Inspection Machines , particularly systems utilizing SVIM (Seidenader Vision Inspection Module) .

When not performing subject matter expert (SME) responsibilities related to vision systems, the engineer will provide general manufacturing engineering support to ensure reliable and efficient production operations.

Key Responsibilities

  • Serve as a Subject Matter Expert (SME) for pharmaceutical visual inspection systems and machine-vision technologies.
  • Perform hands-on setup, tuning, optimization, troubleshooting, and qualification support for Körber/Seidenader Visual Inspection Machines.
  • Configure and optimize SVIM camera inspection hardware and associated vision inspection parameters.
  • Work with SVObserver software for configuring, operating, and optimizing machine-vision inspection systems.
  • Troubleshoot vision-system issues related to cameras, lighting, image quality, inspection parameters, and equipment performance.
  • Optimize inspection systems to improve detection capability, accuracy, repeatability, and overall equipment performance .
  • Support equipment changeovers, new product introductions, process improvements, and vision-system modifications.
  • Participate in investigations related to vision-system failures, inspection defects, deviations, and equipment performance issues.
  • Support root cause analysis (RCA) and implementation of corrective and preventive actions (CAPA), as applicable.
  • Provide technical support during equipment qualification, validation, commissioning, and startup activities.
  • Develop and maintain technical documentation, troubleshooting guides, procedures, and other engineering documentation.
  • Collaborate with Manufacturing, Quality, Validation, Automation, Maintenance, and other cross-functional teams.
  • Provide general manufacturing engineering support when vision-system SME activities are not required.
  • Identify opportunities to improve equipment reliability, process efficiency, inspection performance, and manufacturing throughput.
  • Provide hands-on support on the manufacturing floor and respond to production-related technical issues as needed.

Required Qualifications

  • Hands-on experience with Körber (formerly Seidenader) Visual Inspection Machines .
  • Strong practical experience tuning and optimizing pharmaceutical visual inspection equipment .
  • Experience with SVIM (Seidenader Vision Inspection Module) is highly preferred.
  • Experience working with SVObserver or comparable vision-system configuration/operating software.
  • Strong understanding of machine-vision principles, including:
  • Camera systems
  • Lighting
  • Image acquisition
  • Image quality
  • Inspection parameters
  • Defect detection
  • Vision-system troubleshooting and optimization
  • Experience supporting manufacturing equipment in a GMP/pharmaceutical manufacturing environment .
  • Strong troubleshooting and problem-solving skills.
  • Ability to work hands-on in a manufacturing environment and collaborate with cross-functional teams.

Preferred Qualifications

  • Experience with alternative machine-vision platforms such as Cognex, Omron , or similar systems.
  • Candidates with strong experience in other vision platforms will be considered if they can demonstrate that their skills are transferable to Körber/Seidenader and SVIM systems .
  • Experience with equipment qualification, validation, commissioning, and startup.
  • Experience with deviation investigations, root cause analysis, and CAPA.
  • Experience with automated pharmaceutical inspection and packaging equipment.
  • General manufacturing engineering experience within a regulated environment.

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