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Vision Engineer

Job in Farmington Hills, Oakland County, Michigan, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-08-30
Job specializations:
  • Engineering
    Automation & Mechatronics Engineer, Systems Engineer, Manufacturing Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 105000 USD Yearly USD 80000.00 105000.00 YEAR
Job Description & How to Apply Below

The Vision Engineer provides technical and compliance support to pharmaceutical manufacturing and packaging operations using vision systems, leading vision/automation projects across multiple site locations while delivering timely, professional, and safe support.

Scope of the Role
  • Support equipment purchases and modifications to improve productivity or enable new formulations/products.
  • Ensure compliance with FDA cGMP regulations across design, specification, qualification, validation, maintenance, and use of equipment systems.
  • Complete capital/expense projects within agreed timelines, scope, and budget; manage and track project costs.
  • Participate in change management to assess impacts on validation status of control systems.
  • Support quality initiatives via CAPA and implement new technology to resolve issues.
  • Identify opportunities to improve production processes, focusing on detection and downtime reduction.
  • Coordinate with engineering, maintenance, operations, IT, and scheduling to implement changes and resolve issues.
  • Respond to emergencies and troubleshoot machine performance/efficiency.
  • Design and implement features/technologies to enhance operability, efficiency, safety, quality, and data tracking.
  • Provide strategic plans to upgrade aging/obsolete systems.
  • Review new equipment technical specifications to ensure automation hardware/software align with standards.
Experience Required
  • Bachelor’s degree in an engineering discipline.
  • 3+ years troubleshooting and working with vision systems.
  • Working knowledge of AutoCAD; ability to read drawings/flowcharts/schematics for system design documentation.
  • Experience with computer system validation and change management in an FDA-regulated environment.
  • Experience/familiarity with cGMP.
  • Excellent problem-solving, decision-making, and deadline management in a team environment.
  • Demonstrated ability to interface with multiple departments, consultants, and contractors.
Preferred
  • Lean and Six Sigma knowledge and continuous improvement experience.
  • Prior electrical troubleshooting skills.
  • Experience with PLC programming and troubleshooting.
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