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Fda Inspector Jobs in Minneapolis, MN (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 ...

Fiagon NA, LLC

Be Seen First

Logistics and Service Coordinator

White Bear Lake, MN · On-site

$29 - $34/hr

Perform shipping, receiving, inspect, unload, store, and deliver all materials/products. purchasing ... Maintain an organized and efficient warehouse and additional working areas. complying with FDA, ISO ...

Aerotek

Cnc Swiss Machinist

Lakeville, MN

$21.25 - $29/hr

Perform in-process and final inspections of parts to verify they meet required tolerances ... Follow and support FDA and ISO standards, procedures, and documentation requirements throughout the ...

Actalent

Technician/Junior Engineer

Maple Grove, MN

$30 - $40/hr

Experience operating MicroVu Vision systems and programming MicroVu inspection routines. * Exposure to quality systems within ISO and FDA-regulated environments. * Understanding of GD&T (Geometric ...

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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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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.

Principal Regulatory Affairs Specialist - Bracco Medical Technologies

Acist Medical Systems Inc.

Eden Prairie, MN • On-site

$131 - $143/hr

Other

Medical, Retirement, PTO

Posted 18 days ago

Job description

Why Join Bracco Medical Technologies?

We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way. Each member of the Bracco Medical Technologies team has the power to make a difference......every day!

About the Role

The Principal Regulatory Affairs Specialist develops and executes regulatory strategies for medical device products, submissions, and lifecycle changes. This role provides hands-on regulatory support for new product marketing submissions, changes to existing devices, global registrations, audits, labeling, and ongoing compliance with applicable regulations and company standards.

What You’ll Do
  • Develop and execute regulatory plans for product submissions, including 510(k) Premarket Notifications, EU MDR Technical Documentation, Canadian Licensing Submissions, and select Japan/China submission content.
  • Serve as the regulatory representative on cross-functional project teams throughout the product lifecycle, providing strategic guidance on global regulatory requirements.
  • Prepare for and support communications with regulatory agencies and Notified Bodies, including FDA interactions, submission reviews, approvals, audits, and inspections.
  • Maintain complete and current regulatory files, product registrations, and supporting documentation.
  • Review device labeling, advertising, and promotional materials for compliance with approved submissions and applicable global regulations.
  • Monitor new and changing regulations, assess business impact, and recommend appropriate compliance actions.
  • Mentor junior regulatory staff and provide regulatory guidance to cross-functional partners.
What You’ll Bring
  • Bachelor’s degree in Engineering, Life Sciences, Regulatory Affairs, or a related technical field.
  • 7+ years of regulatory affairs experience in the medical device industry.
  • Demonstrated experience preparing and supporting global regulatory submissions, including FDA 510(k), EU MDR/CE Marking, and Health Canada submissions.
  • Strong understanding of FDA regulations, EU MDR, international regulatory frameworks, product lifecycle requirements, labeling review, and regulatory compliance practices.
  • Experience leading or supporting FDA meetings, agency interactions, audits, inspections, and cross‑functional regulatory strategy discussions.
  • Excellent technical writing, communication, project leadership, analytical thinking, and stakeholder management skills.
Preferred Qualifications
  • Experience supporting Class II medical devices, global market expansion, or multi‑region regulatory submissions.
  • Experience mentoring regulatory professionals or leading regulatory workstreams without direct supervisory authority.
  • Regulatory Affairs Certification or advanced degree in a relevant discipline.
Compensation & Total Rewards

The estimated base salary range for this position is $131,000–$143,000 annually. Actual compensation may vary based on relevant experience, skills, education, internal equity, and business needs.

Bracco Medical Technologies also offers a comprehensive total rewards package, including

  • health benefits
  • paid time off
  • company holidays
  • paid family leave
  • retirement savings
  • tuition reimbursement
  • professional development opportunities

Bracco Medical Technologies is an Equal Opportunity Employer.

Employment decisions are made without regard to race, color, religion, sex, national origin, disability, protected veteran status, age, or any other characteristic protected by applicable law.

Improve people’s lives by shaping the future of prevention and precision imaging. This is our purpose. Our work impacts millions of people all over the world. Not least the more than 4,000 Bracco colleagues who work to improve lives every single day. That is quite a responsibility and something we proudly embrace. We are the Bracco Group!

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