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Fda Inspector Jobs in Norfolk, VA (NOW HIRING)

Instant Systems Inc

Process Engineer

Norfolk, VA

Ensure compliance with FDA, ISO 13485, and other applicable regulatory requirements. * Train ... Participate in audits and inspections, providing technical support and documentation as needed.

Instant Systems Inc

Process Engineer

Norfolk, VA · On-site

Ensure compliance with FDA, ISO 13485, and other applicable regulatory requirements. * Train ... Participate in audits and inspections, providing technical support and documentation as needed.

Accendra Health, Inc.

BRANCH LOG SUPV - NO CDL

Hampton, VA · On-site

$51K - $54K/yr

... inspections and reports, and maintenance regulations. * Schedules Delivery employees on a daily and ... Knowledge of DOT, FDA, and OSHA regulations * Time management skills * Successful completion of ...

Accendra

BRANCH LOG SUPV - NO CDL

Hampton, VA · On-site

$51K - $54K/yr

... inspections and reports, and maintenance regulations. * Schedules Delivery employees on a daily and ... Knowledge of DOT, FDA, and OSHA regulations * Time management skills * Successful completion of ...

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Showing results 21-29

All JobsFda Inspector JobsFda Inspector Jobs in Norfolk, VA

Fda Inspector information

See Norfolk, VA salary details

$23.7K

$53.2K

$95.8K

How much do fda inspector jobs pay per year?

As of Aug 20, 2026, the average yearly pay for fda inspector in Norfolk, VA is $53,156.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,200.00 and $61,400.00 per year, depending on experience, location, and employer.

What does an FDA inspector do?

An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.

What skills and qualifications are needed to be an FDA inspector?

To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.

What types of facilities or products do FDA inspectors review, and what does a typical inspection process involve?

FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.

How do you become an FDA inspector?

To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must pass a written exam and a background check, and often undergo specialized training at the FDA's training center. Certification or licensing is not required but can enhance prospects in the field.

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What job categories do people searching Fda Inspector jobs in Norfolk, VA look for?

The top searched job categories for Fda Inspector jobs in Norfolk, VA are:

What cities near Norfolk, VA are hiring for Fda Inspector jobs?

Cities near Norfolk, VA with the most Fda Inspector job openings:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Norfolk, VA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $53,156 per year, or $25.6 per hour.

Process Engineer

Instant Systems Inc

Norfolk, VA

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 3 days ago

Job description

We are seeking a highly motivated and detail-oriented Process Engineer to join our team. This role is responsible for developing, optimizing, and maintaining manufacturing processes to ensure high-quality production of single use supplies including medical device components. The ideal candidate will have hands-on experience in a manufacturing environment, with a strong background in process engineering, lean manufacturing, and quality systems within a regulated industry.

Responsibilities:

    • Develop, implement, and optimize manufacturing processes
    • Troubleshoots and resolves hardware manufacturing, quality and test issues to support production schedules.
    • Provide corrective actions to fix tooling to minimize downtimes
    • Conduct process validation activities including writing and executing IQ/OQ/PQ Improves manufacturing processes, documentation, yield and test efficiency in collaboration with a multi-disciplined team.
    • Translates engineering design requirements into manufacturing operations sheets, work instructions, tooling and test equipment, workflows and processes.
    • Design, develop, and implement new manufacturing equipment, fixtures, and tools to enhance production capabilities
    • Dispositions non-conforming material with root cause, corrective action and defect analysis as required to prevent recurrence.
    • Reviews design drawings for manufacturability and cost (DFM, DFC).
    • Analyze production data to identify trends, inefficiencies, and opportunities for improvement.
    • Collaborate with cross-functional teams to support new product introductions and process scale-up.
    • Drive continuous improvement initiatives using Lean, Six Sigma, and other methodologies.
    • Troubleshoot process issues and conduct root cause analysis and corrective/preventive actions (CAPA).
    • Support equipment selection, installation, and qualification.
    • Maintain and update process documentation including SOPs, work instructions, and risk assessments.
    • Ensure compliance with FDA, ISO 13485, and other applicable regulatory requirements.
    • Train production staff on new processes, equipment, and best practices.
    • Monitor and improve process yields, cycle times, and overall equipment effectiveness (OEE).
    • Participate in audits and inspections, providing technical support and documentation as needed.
    • Evaluate and implement automation solutions to improve process reliability and reduce labor costs.
    • Manage small to medium-scale engineering projects from concept through execution.
      • Other responsibilities as assigned

To be considered you’ll need:

  • a Bachelor’s degree in STEM
  • a minimum of 5 years of relevant work experience within the medical device or other regulated manufacturing environment.
  • Strong multidisciplined engineering aptitude, analytical skills and problem-solving skills.
  • Experience with Lean Manufacturing and Continuous Improvement activities
  • Proficiency with CAD modeling tools
  • Strong organization skills with the ability to manage multiple tasks simultaneously.
  • Proficient use of Microsoft Office suite (Excel, PowerPoint, Word
  • strong knowledge of lean manufacturing, Six Sigma, and statistical process control (SPC).
  • experience with validation protocols (IQ/OQ/PQ) and risk management tools (FMEA).
  • solid company-centric ideology.
  • creative problem-solving skills.
  • core values of honesty and respect.
  • a thirst for learning.
  • the desire to be challenged.

You will thrive if you:

  • enjoy an autonomous work environment.
  • have a LEAN mindset.
  • are the first person to help.
  • seek out opportunities to bring added value.

Company Benefits & Perks

  • 401K
  • Health Benefits: Medical, Dental, Vision
  • Wellness Program
  • Life Insurance
  • Corporate Sponsored Events
  • Skill growth opportunities
  • Short Term Disability
  • Ability to Advance
  • Working with energetic & creative problem solvers
  • A mission worthy of your energy and expertise

Applicants for this position must successfully pass background, drug screen and reference check. It is impossible to list every requirement for, or responsibility of, any position. Similarly, we cannot identify all the skills a position may require since job responsibilities and the Company's needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.

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