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Fda Inspector Jobs in Tempe, AZ (NOW HIRING)

Ensure inspections are performed in alignment with company SOPs, ISO 13485, FDA 21 CFR Part 820, and customer requirements. * Support internal and external audits with inspection data and records ...

Ensure inspections are performed in alignment with company SOPs, ISO 13485, FDA 21 CFR Part 820, and customer requirements. * Support internal and external audits with inspection data and records ...

Compliance and Regulatory Adherence : • Follow FDA, AATB, and internal regulatory requirements applicable to tissue processing and inspection activities. • Support audit and inspection readiness ...

DEA, FDA) inspections. * Follow up on audits to assure that action plans are developed and completed in a timely fashion. * Assist with management review and associated metrics for the plant

DEA, FDA) inspections. * Follow up on audits to assure that action plans are developed and completed in a timely fashion. * Assist with management review and associated metrics for the plant

DEA, FDA) inspections. * Follow up on audits to assure that action plans are developed and completed in a timely fashion. * Assist with management review and associated metrics for the plant

Pharmacy Technician

Phoenix, AZ · On-site

$20 - $25/hr

Operating from state-of-the-art, FDA-inspected facilities in Chandler and Deer Valley, Arizona ... Participate in visual inspection, lot reconciliation, and inventory management tasks. * Follow ...

Job Page

Phoenix, AZ · On-site

$52K/yr

Tobacco Compliance Inspector Job Location: Address: 150 N 18th Ave, Phoenix, AZ 85007 Posting ... Department of Health and Human Services, Food and Drug Administration (FDA), under the authority of ...

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Fda Inspector information

See Tempe, AZ salary details

$23.8K

$53.5K

$96.3K

How much do fda inspector jobs pay per year?

As of Aug 15, 2026, the average yearly pay for fda inspector in Tempe, AZ is $53,464.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,500.00 and $61,800.00 per year, depending on experience, location, and employer.

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.

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.

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 the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

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 job categories do people searching Fda Inspector jobs in Tempe, AZ look for?

The top searched job categories for Fda Inspector jobs in Tempe, AZ are:

What cities near Tempe, AZ are hiring for Fda Inspector jobs?

Cities near Tempe, AZ with the most Fda Inspector job openings:

Infographic showing various Fda Inspector job openings in Tempe, AZ as of August 2026, with employment types broken down into 76% Full Time, 11% Part Time, 12% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $53,396 per year, or $25.7 per hour.

Quality Inspector Metrology

Cinova Medical

Phoenix, AZ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago


Job description

Position Summary


The Quality Inspector – Metrology is responsible for performing dimensional and visual inspection of injection-molded medical device components to ensure compliance with customer specifications, engineering drawings, and quality standards. This role requires strong metrology and inspection skills and serves as the first line of defense in identifying nonconformances and preventing defective product from advancing through production or reaching customers. The inspector operates precision measurement equipment, including CMM and vision measurement systems, and must adhere to Good Documentation Practices (GDP) at all times to ensure accuracy, traceability, and compliance with ISO 13485 and FDA requirements. This is a 2nd shift position (3:00 PM to 11:30 PM, Monday through Friday). The Quality Inspector may be assigned other tasks at the direction of the Quality Manager and must be willing to work overtime or alternate shifts as needed to support production and quality requirements.


Essential Duties and Responsibilities:

  • Perform routine dimensional and visual inspections of molded medical device components on the production floor and in the quality lab.
  • Use precision metrology equipment (e.g., calipers, micrometers, height gages, pin gauges, go/no-go gauges, optical comparators, vision systems, and CMMs) to verify part conformance to specifications.
  • Operate advanced measurement systems, including Keyence LM-X Series and IM Series, RAM Sprint CNC, Zeiss Spectrum II (TP20), and Micro-Vu Vertex 26 equipment.
  • Interpret engineering drawings, GD&T, critical dimensions, and tolerance schemes related to molded components.
  • Conduct in-process inspections at molding machines to verify part conformity, including visual checks for flash, short shots, splay, contamination, and other molding defects.
  • Follow standardized inspection plans, control plans, sampling plans, and work instructions designed for medical device manufacturing.
  • Record inspection results accurately on check sheets, inspection logs, device history records (DHRs), or within electronic quality systems.
  • Document and segregate nonconforming product, initiating Nonconformance Reports (NCRs) as needed, and support nonconformance documentation with accurate, objective dimensional data.
  • Ensure traceability and proper labeling of inspected product.
  • Ensure inspections are performed in alignment with company SOPs, ISO 13485, FDA 21 CFR Part 820, and customer requirements.
  • Support internal and external audits with inspection data and records.
  • Assist with routine calibration checks and proper care of metrology instruments.
  • Support Gage R&R studies and measurement system analysis under guidance from Quality Engineering.
  • Promote Good Documentation Practices (GDP) and adherence to cleanroom and GMP guidelines.
  • Maintain proper control of quality records as defined by the Quality Management System.
  • Maintain an organized, clean, and GMP-compliant work area.
  • Perform any other duties necessary to support the quality function as assigned by the Quality Manager.


Qualifications:


To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • High school diploma or equivalent required; technical training in Quality, Metrology, or Plastics Manufacturing preferred.
  • Strong metrology and inspection skills required, including proficiency with common inspection tools (calipers, micrometers, height gages, pin gauges, etc.).
  • Experience with Keyence LM-X Series, Keyence IM Series, RAM Sprint CNC, Zeiss Spectrum II TP20, and Micro-Vu Vertex 26 equipment preferred.
  • Experience programming CMM and vision measurement systems is a plus.
  • Solid knowledge of GD&T (Geometric Dimensioning & Tolerancing) and blueprint reading.
  • Ability to follow written procedures and maintain documentation discipline in a regulated (ISO 13485 / FDA) environment.
  • Must be able to read, write, and speak English fluently to ensure accurate documentation and effective communication.
  • Strong attention to detail, organizational skills, and ability to work independently in a fast-paced environment.
  • Good communication skills to effectively interface with production and engineering teams.
  • Basic knowledge of Microsoft Word and Excel; familiarity with Minitab is a plus.
  • Ability to work the 2nd shift schedule (3:00 PM to 11:30 PM, Monday through Friday), with overtime as needed.


Cinova Medical offers competitive pay

Benefits: Medical; Dental; Vision; Life; STD; LTD; 401(k) with company match; Paid Time Off

This is a 2nd shift position. The hours are 3:00pm-11:30pm Mon-Fri.


Cinova Medical, Inc. is an EOE AA M/F/Vet/Disability Employer and Drug Free Workplace.

Upon hire, Cinova Medical, Inc. uses E-Verify to verify employment eligibility for roles based in the United States.