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Visual Inspection Engineer Pharmaceutical Jobs (NOW HIRING)

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Support audit readiness and inspection preparation efforts. * Assist with continuous improvement ... engineering, validation, or C&Q-related activities. * Previous experience in pharmaceutical ...

Acuren

Visual Inspector - CWI

Indianapolis, IN · On-site

... inspection, traditional and advanced NDE/NDT, failure analysis, rope access, materials engineering ... pharmaceutical, aerospace and automotive industries. Acuren employs over 4,000 dedicated ...

INCOG

Inspection Supervisor, 2nd shift

Fishers, IN · On-site

... Engineering or Science or 8 years related experience in the development or support of pharmaceutical inspection processes, quality systems or a closely related field. * Must pass health and visual ...

Eli Lilly and Company

NC · On-site

During the project phase, the Visual Inspection Technician will support commissioning/qualification ... Flexibility and problem-solving skills * 2+ years relevant experience in pharmaceutical, or ...

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How much do visual inspection engineer pharmaceutical jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for visual inspection engineer pharmaceutical in the United States is $35.10, according to ZipRecruiter salary data. Most workers in this role earn between $25.96 and $42.79 per hour, depending on experience, location, and employer.

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

AspectVisual Inspection Engineer PharmaceuticalQuality Control Inspector Pharmaceutical
CredentialsTypically requires a degree in life sciences or engineering, with certifications in GMP or quality assuranceOften requires a high school diploma or associate degree, with certifications in GMP or quality standards
Work EnvironmentWorks in cleanrooms and manufacturing areas inspecting pharmaceutical productsWorks in laboratories or production lines performing quality checks
Industry UsageCommonly employed in pharmaceutical manufacturing for product quality assuranceUsed across pharmaceutical companies for routine quality inspections

The Visual Inspection Engineer Pharmaceutical focuses on detailed visual assessments of pharmaceutical products, often requiring specialized training and engineering knowledge. In contrast, the Quality Control Inspector Pharmaceutical performs routine quality checks, typically with less technical training. Both roles are essential for ensuring product safety and compliance within the pharmaceutical industry.

Infographic showing various Visual Inspection Engineer Pharmaceutical job openings in the United States as of May 2026, with employment types broken down into 79% Full Time, 19% Part Time, and 2% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $73,007 per year, or $35.1 per hour.

Compliance Engineer | Pharmaceutical | C&Q

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR • On-site

Full-time

Posted 18 days ago

Job description

Location: On Site
Industry: Pharmaceutical Manufacturing – Solid Dosage

We are seeking a motivated and detail-oriented Compliance Engineer to support projects and operations within a GMP-regulated pharmaceutical manufacturing environment. This role will focus on ensuring compliance, supporting C&Q-related activities, and partnering with cross-functional teams to maintain quality standards and operational excellence.

The ideal candidate will bring experience in pharmaceutical manufacturing environments and enjoy working in collaborative, fast-paced settings that support engineering and manufacturing initiatives.

Main Responsibilities

  • Support compliance activities related to pharmaceutical engineering and C&Q projects.
  • Partner with Project Execution and Engineering teams to support investigations and follow-up activities when needed.
  • Assist with CAPA-related actions and support timely completion of quality initiatives.
  • Monitor compliance-related metrics and help track completion of key quality activities.
  • Review and support GMP documentation to ensure quality and compliance standards are met.
  • Participate in change control, documentation review, and quality system activities.
  • Support onboarding activities and coordinate documentation for new team members.
  • Collaborate with Quality, Manufacturing, Engineering, and Validation teams.
  • Support audit readiness and inspection preparation efforts.
  • Assist with continuous improvement initiatives and process enhancement activities.
  • Maintain accurate documentation and ensure compliance with internal procedures.
General Requirements
  • Knowledge of GMP regulations and pharmaceutical compliance practices.
  • Familiarity with Commissioning & Qualification (C&Q) processes and validation activities.
  • Understanding of quality systems, documentation practices, CAPA, and change management.
  • Strong organizational and communication skills.
  • Ability to work independently and within cross-functional teams.
  • Strong attention to detail and problem-solving mindset.
  • Proficiency with Microsoft Office and electronic documentation systems.
  • Experience with documentation platforms such as Kneat or similar systems is a plus.
Education
  • Bachelor’s degree in Engineering (Chemical, Mechanical, Industrial, Biomedical, Electrical, or related field)
  • Life Sciences or related technical discipline
  • Equivalent experience in pharmaceutical environments may be considered.

Experience

  • Minimum 3+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments.
  • Experience supporting compliance, quality, engineering, validation, or C&Q-related activities.
  • Previous experience in pharmaceutical manufacturing environments required.
  • Experience in Solid Dosage manufacturing is preferred.
  • Experience with GMP documentation, CAPA, investigations, and quality systems is a plus.
  • Experience supporting manufacturing operations and cross-functional project teams preferred.
Physical Requirements
  • Ability to work in office and manufacturing environments.
  • Ability to walk production areas and support field activities.
  • May require prolonged periods sitting, standing, and computer use.
  • Ability to occasionally lift up to 25 lbs.
  • Ability to wear required PPE and cleanroom attire as needed.