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Fda Inspector Jobs in Minnesota (NOW HIRING)

Trelleborg

NPD Quality Engineer

Delano, MN · On-site

$78K - $97K/yr

ISO13485, 9001, 14971, FDA 21 CFR 820, EU/MDR, ITAR) * Provides periodic work direction and assistance to QA inspectors and QE Technicians * Supports other quality activities such as customer ...

Trelleborg

VP Global Quality and Regulatory

Plymouth, MN · On-site

$220K - $225K/hr

Coordinate FDA/EU or any other country required inspections and audits, respond to findings and maintain records of all activities. Assure that any product detentions are promptly resolved; provide ...

Collabera

MDR/Vigilance Specialist

Moundsview, MN

Develop and maintain product knowledge of CRHF products. Assist in inspection support for FDA and global regulatory agencies. This may include research and preparation of correspondence in response ...

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Fda Inspector information

See Minnesota salary details

$24K

$53.8K

$97K

How much do fda inspector jobs pay per year?

As of Aug 23, 2026, the average yearly pay for fda inspector in Minnesota is $53,808.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,700.00 and $62,200.00 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.

What are popular job titles related to Fda Inspector jobs in Minnesota?

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

What job categories do people searching Fda Inspector jobs in Minnesota look for?

The top searched job categories for Fda Inspector jobs in Minnesota are:

What cities in Minnesota are hiring for Fda Inspector jobs?

Cities in Minnesota with the most Fda Inspector job openings:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 3% Contract, and 2% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $53,808 per year, or $25.9 per hour.

NPD Quality Engineer

Trelleborg Healthcare & Medical Tustin

Delano, MN

$78K - $97K/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago

Job description

Trelleborg Medical Solutions is seeking a NPD Quality Engineer to join their team. The NPD Quality Engineer is responsible to plan and coordinate quality engineering activities for medical device manufacturing through the design and development phases including validation for new product development. Collaborate with other New Product Development (NPD) teams to support equipment qualification, software validation, test method development/validation, process development/validation (IQ/OQ/PQ), and other quality processes to ensure compliance with the company's Quality System and applicable external requirements and standards, including FDA, ISO 13485, and/or other regulatory agencies as applicable to medical device manufacturing. Working with internal and external customers to support creative approaches and solutions to problems.

As a valued team member with Trelleborg, you will enjoy:

  • Competitive compensation: $78,000 - $97,000 Annual Salary
  • Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement, and more!
  • Clean work environment: Enjoy working in a very clean and climate-controlled environment every day!
  • Greater opportunity for impact: You will have the autonomy and support to lead the production team and impact the production of life-saving devices.
  • Growth and advancement: Join a global company that loves to promote from within and allows for advancement.

    Qualifications:

    Required

    •  4-year degree in quality, engineering or any related field
    • 2+ years in a manufacturing environment in a technical support role

    Desired:

    • ASQ Certified Quality Engineer

    • Formal Six Sigma Yellow/ Green belt training

    • Knowledge and experience with GMP/ISO Standards: ISO 9000/9001, ISO 13485, and FDA 21CFR 820/11 (4/210/211 as applicable), EU/MDR.

     Responsibilities:

    • Knowledgeable and adheres to TMS Quality Management System and its requirements.

    • Works with the NPD team to plan, develop and execute equipment, software, test method, and/or process validation strategy

    • Monitors and reports out on project deliverables to ensure timely completion; escalates issues, questions, and concerns, immediately to prevent project delays.

    • Performs risk management by identifying, estimating, evaluating, controlling, and monitoring risk, utilizing risk tools such as Process Failure Modes and Effects Analysis (pFMEA)

    • Authors or approves protocols and reports for Equipment Qualification (IQ/EQ), Software validation (SV), Test Method Validation (TMV), Process validation (OQ/PQ). · Reviews and evaluates specifications, drawings, quality agreements, customer documentation and other documents as necessary to support NPD projects

    •  Plans, coordinates, and oversees Test Method Development activities; initiates inspection plans for new/revised product.

    •  Works with the Metrology team to recommend equipment, sampling plans, and measurement techniques for inspection specifications

    •  Performs measurement system analysis (MSA) Gage 1, Gage Repeatability and Reproducibility (GRR), Bias and Linearity, Resolution and Stability studies

    •  Performs statistical analysis of inspection data, process characterization, design of experiments (DOE) results, ANOVA, Capability Analysis

    •  Authors and executes Quality Plans, when needed · Support resolution of deviations and nonconforming issues arising during development; completes investigations and perform root cause analysis.

    • Reviews and ensures compliance with QMS of all validation documents and records

    • Supports Engineering, Manufacturing, and Inspection personnel in design, methods, tooling, validations, and other areas related to the control of product

    • Communicates with customers on clarification of specifications, completing customer documents, complaints, process changes, and other projects, as needed. 

    • Understands regulatory requirements (e.g. ISO13485, 9001, 14971, FDA 21 CFR 820, EU/MDR, ITAR)

    • Provides periodic work direction and assistance to QA inspectors and QE Technicians

    • Supports other quality activities such as customer complaints, MRBs, and CAPAs

    • Drives best practices through the application of effective quality engineering principles and procedures across functions.

    • Supports internal and external audits.

    • Other duties as assigned.

    Apply