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Automated Visual Inspection Jobs (NOW HIRING)

Magna

Group AI Technical Specialist

Lancaster, OH

This role provides technical leadership across manufacturing divisions including automated visual inspection, welding, assembly, robotics, controls, and operational technology (OT). This position ...

Magna

Group AI Technical Specialist

Lancaster, OH · On-site

This role provides technical leadership across manufacturing divisions including automated visual inspection, welding, assembly, robotics, controls, and operational technology (OT). This position ...

FUJIFILM Biotechnologies

Manual and/or automated visual inspection.Support projects that improve Drug Product manufacturing processes, including:Training of new colleagues.Maintaining cGMP documentation.Assisting in ...

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Automated Visual Inspection information

What is automated visual inspection?

Automated visual inspection is a process where machines, often equipped with cameras and artificial intelligence, are used to examine products or components for defects or quality issues. This technology allows for high-speed, consistent, and accurate inspections without human intervention. It is widely used in manufacturing industries to improve product quality, reduce errors, and increase efficiency. Automated visual inspection systems can detect surface flaws, incorrect assembly, or other anomalies that might affect the final product.

What are the key skills and qualifications needed to thrive in automated visual inspection?

To excel in Automated Visual Inspection, you need a background in engineering or quality control, strong analytical abilities, and familiarity with inspection processes. Experience with machine vision systems, image processing software, and knowledge of automation tools like PLCs or robotics is highly valuable. Attention to detail, problem-solving skills, and effective communication help professionals identify defects and collaborate with production teams. These competencies ensure high product quality, efficient operations, and minimal production errors in manufacturing environments.

What are some common challenges faced in an automated visual inspection role, and how can they be addressed?

Professionals in Automated Visual Inspection often encounter challenges such as dealing with varying product defects, adapting to changes in manufacturing processes, and ensuring the inspection system remains accurate over time. Addressing these challenges typically involves continuous calibration of equipment, close collaboration with process engineers, and regular updates to the inspection algorithms. Proactively communicating with cross-functional teams and staying current with advancements in machine vision technology can also help ensure high-quality and efficient inspections.

What is the difference between Automated Visual Inspection vs Quality Control Inspector?

AspectAutomated Visual InspectionQuality Control Inspector
CredentialsTypically requires technical training or certifications in automation or imaging systemsOften requires quality assurance certifications or experience in inspection methods
Work EnvironmentPrimarily uses machines, cameras, and software in manufacturing or production settingsWorks directly with products, inspecting manually or with basic tools in manufacturing or warehouse settings
Industry UsageCommon in electronics, automotive, and manufacturing industries for rapid defect detectionUsed across various industries for manual inspection and quality assurance

Automated Visual Inspection involves using machines and software to automatically detect defects, offering speed and consistency. In contrast, Quality Control Inspectors perform manual inspections, relying on their judgment to ensure product quality. Both roles are essential in manufacturing but differ in tools, training, and approach.

Infographic showing various Automated Visual Inspection job openings in the United States as of September 2026, with employment types broken down into 72% Full Time, 4% Part Time, 2% Temporary, 11% Contract, and 11% Nights. Highlights an 100% In-person job distribution.

Validation Engineer III - OSD/Packaging/AVI

Greenville, NC • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees
Learn more about Thermo Fisher Scientificexternal

Full-time

Re-posted yesterday

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 430 frontline employees who took The Breakroom Quiz

171st of 547 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe, and helping find cures for cancer.
At our Greenville, North Carolina site, you'll join a highly collaborative Validation Engineering team supporting pharmaceutical manufacturing operations. Our team plays a critical role in ensuring manufacturing processes are validated, compliant, and capable of consistently producing high-quality medicines that improve lives around the world.
Discover Impactful Work
As a Validation Engineer III, you will support manufacturing process validation activities focused primarily on Oral Solid Dose (OSD) continuous manufacturing and pharmaceutical packaging operations. You'll lead validation efforts from protocol development through execution and final reporting while partnering with Manufacturing, Engineering, Quality, and Technical Operations teams.
This role offers an excellent balance of technical documentation and hands-on manufacturing support, allowing you to contribute directly to product launches, process improvements, and regulatory compliance. In addition to OSD process and packaging validation, you'll have opportunities to support Automated Visual Inspection (AVI) validation activities as business needs require.
A Day in the Life
This position offers approximately:
  • 70% desk-based work
    • Write validation protocols and supporting documentation
    • Perform data analysis and calculations
    • Prepare validation summary reports
    • Conduct data review and documentation review
    • Support investigation and technical problem solving
  • 30% manufacturing floor execution
    • Execute manufacturing process validation protocols
    • Perform packaging process validation activities
    • Collect validation samples and process data
    • Partner with Manufacturing and Quality during validation campaigns
    • Support Automated Visual Inspection (AVI) validation activities when needed
Key Responsibilities
  • Lead manufacturing process validation activities for Oral Solid Dose (OSD) pharmaceutical products.
  • Develop, execute, and document validation protocols, including IQ, OQ, and PQ.
  • Perform packaging process validation for commercial pharmaceutical manufacturing.
  • Analyze validation data and prepare technical reports that support regulatory compliance.
  • Support cleaning validation activities as part of overall manufacturing process qualification.
  • Collaborate with Manufacturing, Engineering, Quality, and Technical Operations teams to execute validation projects.
  • Participate in peer review of validation documentation and data.
  • Support Automated Visual Inspection (AVI) validation activities as assigned.
  • Contribute to continuous improvement initiatives that enhance manufacturing performance and compliance.
  • Support internal audits, customer audits, and regulatory inspections.
Keys to Success
Education
  • Bachelor's degree in Engineering, Life Sciences, Chemistry, or another technical discipline.
  • Advanced degree preferred.
Experience
  • Bachelor's degree with 5+ years of validation experience, or an advanced degree with 3+ years of validation experience within pharmaceutical, biotechnology, or another regulated manufacturing environment.
  • Experience developing and executing validation protocols in GMP manufacturing.
  • Experience with IQ/OQ/PQ documentation and execution.
Preferred Experience
Candidates with the following experience will be especially successful in this role:
  • Oral Solid Dose (OSD) manufacturing process validation
  • Continuous Manufacturing (CM)
  • Packaging process validation (preferred over equipment-only validation)
  • Automated Visual Inspection (AVI)
  • Sterile packaging validation
  • Cross-functional collaboration within pharmaceutical manufacturing
Knowledge, Skills & Abilities
  • Strong knowledge of FDA cGMP regulations and pharmaceutical manufacturing practices.
  • Experience with manufacturing process validation, equipment qualification, utilities, cleaning processes, and computer systems.
  • Strong technical writing and documentation skills.
  • Experience performing validation data analysis and interpretation.
  • Excellent analytical and problem-solving skills.
  • Strong communication and collaboration skills with cross-functional teams.
  • Proficiency with Microsoft Office and validation documentation systems.
  • Experience supporting regulatory inspections and customer audits is preferred.
  • Knowledge of Lean Manufacturing or continuous improvement methodologies is a plus.
  • Ability to work in cleanroom and manufacturing environments.
  • Flexibility to occasionally support extended hours during validation campaigns.
  • Occasional travel (up to 25%) may be required to support Factory Acceptance Testing (FAT) or other business needs.
Why Join Us?
At Thermo Fisher Scientific, your work directly impacts patients around the world. You'll collaborate with talented colleagues, work on cutting-edge pharmaceutical manufacturing technologies, and gain experience supporting innovative Oral Solid Dose manufacturing, packaging, and validation programs. We invest in our people through professional development, challenging projects, and opportunities to grow your career while making a meaningful difference.

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