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Fda Inspector Jobs in Phoenix, AZ (NOW HIRING)

Dip Mold Operator

Tempe, AZ ยท On-site

$16.50 - $19.75/hr

Perform visual and functional inspections to ensure product quality and compliance with ... FDA Quality System Regulations (21 CFR Part 820), and all company quality procedures. * Maintain a ...

Dip Mold Operator

Tempe, AZ

$16 - $19.50/hr

Perform visual and functional inspections to ensure product quality and compliance with ... FDA Quality System Regulations (21 CFR Part 820), and all company quality procedures. Maintain a ...

Dip Mold Operator

Tempe, AZ

$16 - $19.50/hr

Perform visual and functional inspections to ensure product quality and compliance with ... FDA Quality System Regulations (21 CFR Part 820), and all company quality procedures. * Maintain a ...

Follow Standard Operating Procedures (SOPs) and sanitation schedules to ensure compliance with FDA ... Conduct inspections to verify sanitation effectiveness and report any deficiencies. * Work closely ...

Follow Standard Operating Procedures (SOPs) and sanitation schedules to ensure compliance with FDA ... Conduct inspections to verify sanitation effectiveness and report any deficiencies. * Work closely ...

Perform product inspection from beginning process to packaged product * Perform net weight ... Experience working with USDA/FDA preferred * Good verbal and written communication skills English

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Fda Inspector information

See Phoenix, AZ salary details

$23.4K

$52.5K

$94.5K

How much do fda inspector jobs pay per year?

As of Aug 14, 2026, the average yearly pay for fda inspector in Phoenix, AZ is $52,468.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,800.00 and $60,600.00 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 are popular job titles related to Fda Inspector jobs in Phoenix, AZ?

For Fda Inspector jobs in Phoenix, AZ, the most frequently searched job titles are:

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

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

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

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

Infographic showing various Fda Inspector job openings in Phoenix, AZ as of August 2026, with employment types broken down into 75% Full Time, 12% Part Time, 12% Contract, and 1% Nights. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $54,550 per year, or $26.2 per hour.

Dip Mold Operator

Aptyx

Tempe, AZ โ€ข On-site

$16.50 - $19.75/hr

Full-time

Posted 10 days ago


Job description


Production Operator - Stethoscope Manufacturing
Position Summary
The Production Operator is responsible for manufacturing, assembling, inspecting, testing, and packaging medical device products, including stethoscopes, in accordance with Solventum quality standards, regulatory requirements, and established work instructions. This position ensures products meet customer specifications while maintaining a safe, efficient, and compliant manufacturing environment.
Essential Duties and Responsibilities
  • Assemble stethoscope components according to standardized work instructions.
  • Operate manual, semi-automated, and automated production equipment.
  • Perform visual and functional inspections to ensure product quality and compliance with specifications.
  • Conduct in-process quality checks and accurately document production and inspection results.
  • Read and follow manufacturing procedures, drawings, work instructions, and standard operating procedures (SOPs).
  • Identify and report product defects, equipment issues, or process deviations to the appropriate supervisor.
  • Perform basic equipment setup, cleaning, and preventive maintenance as required.
  • Package finished products according to customer and regulatory requirements.
  • Maintain accurate production records in paper and/or electronic manufacturing systems.
  • Follow Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), ISO 13485 requirements, FDA Quality System Regulations (21 CFR Part 820), and all company quality procedures.
  • Maintain a clean and organized work area using 5S and Lean Manufacturing principles.
  • Comply with all Environmental, Health & Safety (EHS) policies and wear required personal protective equipment (PPE).
  • Participate in continuous improvement initiatives to improve safety, quality, delivery, and productivity.
  • Cross-train in multiple production areas to support operational needs.
  • Perform other duties as assigned.

Qualifications
  • High school diploma or GED required.
  • Previous manufacturing, assembly, or medical device production experience preferred.
  • Ability to read and follow written work instructions and production documentation.
  • Basic computer and data entry skills.
  • Strong attention to detail and commitment to producing high-quality products.
  • Ability to work independently and as part of a team.

Physical Requirements
  • Ability to sit or stand for extended periods.
  • Frequent use of hands and fingers to assemble small components.
  • Good manual dexterity and hand-eye coordination.
  • Ability to distinguish colors and perform detailed visual inspections.
  • Ability to lift up to 25 pounds occasionally.
  • Ability to perform repetitive motions throughout the work shift.

Work Environment
  • Climate-controlled medical device manufacturing environment.
  • May require the use of safety glasses, gloves, hearing protection, and other PPE as applicable.
  • Regular attendance and schedule flexibility, including overtime, may be required to meet production demands.