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Fda Inspector Jobs in Minneapolis, MN (NOW HIRING)

Marshall Mfg Co

Quality Inspector

Minneapolis, MN

$21 - $35/hr

Accurately document inspection results in proper format * Follow good documentation practices ... FDA Regulations * USDA Regulations * Pharmaceuticals * Standard Operating Procedures (SOPs)

Abbott

Quality Inspector II

Minnetonka, MN · On-site

Job Title Quality Inspector II Working at Abbott At Abbott, you can do work that matters, grow, and ... Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ...

Abbott

Quality Inspector II

Minnetonka, MN

Job Title Quality Inspector II Working at Abbott At Abbott, you can do work that matters, grow, and ... Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ...

Jobtailor

Senior Quality Engineer

Chaska, MN · On-site

$110 - $140/hr

Direct experience with FDA inspections, MDSAP audits, ISO 13485 audits * Experience advising senior leadership and applying pre/post market regulations * Knowledge of ISO 14971 Risk Management ...

Laborie

Senior Director Quality

Minneapolis, MN

Act as a primary quality representative during FDA inspections, notified body audits, and customer audits in conjunction with other Quality leadership. * Ensure timely responses to audit observations ...

Integer

100% Inspector

Minneapolis, MN

$20.63 - $30.25/hr

Food and Drug Administration (FDA) regulations, company policies and operating procedures, and ... Assists in the training of new inspectors. * Ensures discrepant material has been properly ...

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All JobsFda Inspector JobsFda Inspector Jobs in Minneapolis, MN

Fda Inspector information

See Minneapolis, MN salary details

$25.6K

$57.3K

$103.3K

How much do fda inspector jobs pay per year?

As of Aug 23, 2026, the average yearly pay for fda inspector in Minneapolis, MN is $57,307.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,200.00 and $66,200.00 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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The top searched job categories for Fda Inspector jobs in Minneapolis, MN are:

What cities near Minneapolis, MN are hiring for Fda Inspector jobs?

Cities near Minneapolis, MN with the most Fda Inspector job openings:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Minneapolis, MN 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 $57,307 per year, or $27.6 per hour.

Senior Quality Engineer, Medical Devices & Compliance

Jobtailor

Chaska, MN • On-site

$110 - $140/hr

Other

Posted 5 days ago

Job description

• Analyze medical device products for compliance to standards
• Participate in the Design Change process
• Author new SOPs and other documentation
• Review and approve Change Orders (COs), Nonconformance Report (NCRs), Corrective and Preventive Action (CAPA) records
• Work within a cross-functional team to support product development
• Perform Design History File audits
• Provide compliance guidance concerning development, application, and maintenance of quality standards
• Prepare, support, and ensure readiness for audits and inspections

Requirements

  • Bachelor of Science (B.S.) degree or higher in engineering
  • At least 5 years of experience in engineering or Quality
  • Direct experience with FDA inspections, MDSAP audits, ISO 13485 audits
  • Experience advising senior leadership and applying pre/post market regulations
  • Knowledge of ISO 14971 Risk Management standard
  • Knowledge of ISO 62304 Life Cycle Requirements for Medical Device Software
  • Knowledge of Medical Electrical Equipment Safety Standards
  • Ability to read, analyze and interpret engineering/technical drawings

🔍 ATS Optimization Keywords
Below are skills and terms extracted directly from this job posting to improve Applicant Tracking System (ATS) visibility. This unique feature helps candidates tailor their applications more effectively — a feature exclusive to JobTailor job listings.

Hard Skills

  • engineering
  • quality assurance
  • compliance analysis
  • SOP authoring
  • design history file audits
  • risk management
  • technical drawing interpretation
  • FDA inspections
  • MDSAP audits
  • ISO 13485

Soft Skills

  • cross-functional teamwork
  • communication
  • leadership advising
  • organizational skills
  • analytical skills
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