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Inspection Engineering Jobs (NOW HIRING)

JC Automation Corp

PR · On-site

$74.80K - $101.40K/yr

Ensure all inspection engineering activities are aligned with cGMP regulations, FDA guidelines, and internal site procedures throughout the product lifecycle. REQUIREMENTS & QUALIFICATIONS Required

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How much do inspection engineering jobs pay per year?

As of May 31, 2026, the average yearly pay for inspection engineering in the United States is $62,788.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,000.00 and $70,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Inspection Engineer, and why are they important?

To thrive as an Inspection Engineer, a solid background in engineering principles, materials science, and quality assurance—often supported by a relevant engineering degree and certifications like API or NDT—is essential. Familiarity with inspection tools, non-destructive testing (NDT) methods, and documentation systems like computerized maintenance management systems (CMMS) is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills that help Inspection Engineers excel in identifying and reporting issues. These competencies ensure the integrity, safety, and compliance of equipment and structures, ultimately minimizing risks and operational downtime.

What are some common challenges faced by inspection engineers and how can they be addressed?

Inspection engineers often encounter challenges such as keeping up with rapidly changing regulatory standards, working in physically demanding environments, and accurately documenting inspection results under tight deadlines. To address these, staying updated through regular training, using advanced inspection technologies, and maintaining clear communication with other engineering and safety teams can be highly beneficial. Building strong relationships with colleagues and prioritizing safety protocols also help ensure thorough and compliant inspections.

What is inspection engineering?

Inspection engineering is a specialized field focused on evaluating and ensuring the safety, reliability, and compliance of equipment, structures, or systems through systematic inspections and assessments. Inspection engineers use various techniques—such as visual checks, non-destructive testing, and data analysis—to identify defects, wear, or non-compliance with standards. Their work is essential in industries like manufacturing, oil and gas, construction, and transportation, where safety and quality are critical. They often also recommend repairs, maintenance, or improvements based on their findings.

What is the difference between Inspection Engineering vs Quality Assurance Engineering?

AspectInspection EngineeringQuality Assurance Engineering
CertificationsASNT, API, NDT certificationsASQ CQE, Six Sigma, ISO certifications
Work EnvironmentField inspections, plant sites, manufacturing facilitiesOffice-based, process development, audits
Employer & Industry UsageManufacturing, oil & gas, aerospaceManufacturing, software, healthcare

Inspection Engineering focuses on the direct examination and testing of products or materials to ensure compliance with standards. Quality Assurance Engineering involves developing and implementing processes to prevent defects and improve quality across production. While both roles aim for quality, Inspection Engineering is more hands-on and inspection-focused, whereas Quality Assurance Engineering emphasizes process improvement and system audits.

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Inspection Engineering jobs near you
Infographic showing various Inspection Engineering job openings in the United States as of May 2026, with employment types broken down into 81% Full Time, 7% Part Time, 1% Temporary, 10% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $62,788 per year, or $30.2 per hour.

Sr Parenteral Inspection Technology Engineer

JC Automation Corp

On-site

$74.80K - $101.40K/yr

Full-time

Posted 13 days ago

Job description

About Company:

JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.


ABOUT THE ROLE

We are seeking a Senior Inspection Technology Engineer to lead inspection engineering activities for sterile and biologics parenteral products. This role combines deep technical expertise in automated inspection systems with hands-on project leadership — from technology development and implementation to validation, line trials, and operational support.

The ideal candidate brings strong problem-solving capabilities, experience in pharmaceutical sterile manufacturing, and the cross-functional collaboration skills needed to align inspection efforts with manufacturing, quality, and validation teams.


RESPONSIBILITIES

  • Inspection Technology Development: Lead the development, deployment, and lifecycle management of new parenteral inspection technologies and automated inspection systems for sterile and biologics products.
  • Process Improvement & Project Leadership: Identify and lead process improvement initiatives related to inspection systems. Manage inspection-related capital or operational projects to maximize efficiency, quality, and compliance.
  • Validation & Line Trials: Execute equipment validation protocols, manage line trials, and support seamless product transfers, ensuring all activities are documented and compliant with regulatory standards.
  • Equipment Troubleshooting: Apply advanced technical problem-solving capabilities to troubleshoot complex inspection equipment and resolve operational bottlenecks in a timely manner.
  • Cross-Functional Collaboration: Partner closely with manufacturing, engineering, quality, and validation teams to ensure inspection systems meet site priorities and stringent regulatory requirements.
  • Regulatory Compliance: Ensure all inspection engineering activities are aligned with cGMP regulations, FDA guidelines, and internal site procedures throughout the product lifecycle.


REQUIREMENTS & QUALIFICATIONS

Required

  • Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical, or Automation), Computer Science, or a related technical discipline.
  • Strong foundation in inspection engineering activities specifically for sterile and biologics parenteral products.
  • Proven track record in the development, deployment, and lifecycle management of automated inspection technologies.
  • Extensive hands-on experience executing equipment validation protocols, managing line trials, and supporting product transfers.
  • Advanced troubleshooting capabilities for complex inspection equipment and control systems.
  • Demonstrated ability to lead process improvements and manage inspection-related projects end-to-end.
  • Experience in pharmaceutical sterile manufacturing environments with knowledge of cGMP and FDA requirements.


Preferred

  • Experience with automated vision inspection systems or machine learning-based inspection technologies.
  • Familiarity with lyophilized parenteral products and associated inspection challenges.
  • PMP or equivalent project management certification.
  • Experience supporting regulatory audits or inspections related to parenteral inspection systems.


SKILLS

Technical Skills

  • Inspection engineering for sterile and biologics parenteral products
  • Automated inspection system development, implementation, and lifecycle management
  • Equipment validation protocols (IQ/OQ/PQ) and line trial execution
  • Advanced troubleshooting of inspection equipment and control systems
  • Process improvement methodologies in regulated manufacturing environments
  • cGMP compliance, FDA guidelines, and regulatory documentation
  • Microsoft Office 365


Soft Skills

  • Strong cross-functional collaboration with manufacturing, quality, and validation teams
  • Technical leadership and subject matter expertise
  • Structured problem-solving and root cause analysis
  • Project management and execution in high-complexity environments
  • Clear technical communication with multidisciplinary stakeholders
  • Adaptability and availability to support other shifts as business needs require