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Customs Inspector Jobs in Miami, FL (NOW HIRING)

LCX Freight USA LLC

Operations Agent

Miami, FL · On-site

... customs documents, manifests, and other shipment paperwork for accuracy and regulatory compliance. * Liaise with partner airlines and relevant authorities to ensure seamless cargo inspections and ...

LCX Freight USA LLC

Operations Agent

Miami, FL · On-site

... customs documents, manifests, and other shipment paperwork for accuracy and regulatory compliance. * Liaise with partner airlines and relevant authorities to ensure seamless cargo inspections and ...

AVCON, INC.

Construction Manager

Fort Lauderdale, FL · On-site

Prepares and maintains inspector daily reports (IDR's) of work-in-progress and provides status ... Ability to obtain security clearance for air operations badging and Customs Border Protection (CBP ...

Banyan Air Service

Crew Support

Fort Lauderdale, FL · On-site

$18/hr

... inspect the vehicle to return the vehicle, A complete knowledge of Ft. Lauderdale's Executive ... Customs, and all other FBOs located at the airport, Airport Authority, Tower and U.S. Customs ...

Banyan Air Service

Crew Support

Fort Lauderdale, FL · On-site

$18/hr

... inspect the vehicle to return the vehicle, A complete knowledge of Ft. Lauderdale's Executive ... Customs, and all other FBOs located at the airport, Airport Authority, Tower and U.S. Customs ...

Holcim

Trading Operator

Coral Gables, FL · On-site

Obtain, issue documentary/shipping instructions, customs documentation, inventory documentation ... inspection, etc. where required. * Ensure nomination and timely acceptance of vessels in close ...

Holcim

Trading Operator

Coral Gables, FL

Obtain, issue documentary/shipping instructions, customs documentation, inventory documentation ... inspection, etc. where required. * Ensure nomination and timely acceptance of vessels in close ...

VIVEX BIOLOGICS INC

Distribution Technician

Miami, FL · On-site

... customs paperwork. * Prepares customer packages for courier pick-ups. * Processes all internal ... and inspections of tissue. * Ensures proper documentation for all tissue inventory transfers.

VIVEX BIOLOGICS INC

Distribution Technician

Miami, FL · On-site

... customs paperwork. * Prepares customer packages for courier pick-ups. * Processes all internal ... and inspections of tissue. * Ensures proper documentation for all tissue inventory transfers.

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Showing results 21-40

All JobsCustoms Inspector JobsCustoms Inspector Jobs in Miami, FL

Customs Inspector information

See Miami, FL salary details

$11

$26

$49

How much do customs inspector jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for customs inspector in Miami, FL is $26.17, according to ZipRecruiter salary data. Most workers in this role earn between $17.69 and $30.10 per hour, depending on experience, location, and employer.

What is a customs inspector?

Customs Inspectors are government officials responsible for enforcing laws and regulations related to the import and export of goods at borders, airports, and seaports. They inspect luggage, cargo, and vehicles to detect illegal or restricted items such as drugs, weapons, and undeclared goods. Customs Inspectors also verify documentation, collect duties and taxes, and help prevent smuggling and trafficking. Their work helps ensure national security and compliance with trade laws.

What are some common challenges customs inspectors face during their daily inspections?

Customs Inspectors often encounter challenges such as identifying concealed or improperly declared items, managing high volumes of travelers or shipments, and staying current with constantly changing regulations. They must balance efficiency with thoroughness, ensuring that they do not disrupt trade or traveler flow while still preventing illegal activities. Additionally, working in diverse environments—from airports to shipping docks—requires strong adaptability and communication skills, especially when collaborating with other agencies or handling stressful situations.

What are the key skills and qualifications needed to thrive as a customs inspector, and why are they important?

To thrive as a Customs Inspector, you need a solid understanding of customs regulations, investigative techniques, and often a bachelor's degree or relevant law enforcement experience. Familiarity with customs processing systems, X-ray scanners, and risk assessment tools is typically required, along with any necessary government certifications. Strong attention to detail, analytical thinking, and effective interpersonal communication are vital soft skills for this role. These competencies ensure the accurate enforcement of laws, facilitate efficient border control, and help prevent illegal activities such as smuggling.

What is the difference between Customs Inspector vs Customs Officer?

AspectCustoms InspectorCustoms Officer
Required CredentialsHigh school diploma or equivalent; specialized training; sometimes certifications in inspection proceduresSimilar credentials; often includes training in customs laws and inspection techniques
Work EnvironmentBorder crossings, airports, ports; inspecting goods and travelersBorder stations, customs offices; enforcing customs regulations
Employer & IndustryGovernment agencies at ports, airports, border crossingsSame as Customs Inspector, often overlapping roles

Customs Inspectors and Customs Officers share similar credentials and work environments, primarily focusing on inspecting goods and travelers at borders and ports. While their roles may differ slightly in scope or specific duties, they are often employed interchangeably within government agencies to enforce customs laws and regulations.

How do you become a customs inspector?

To become a customs inspector, candidates typically need a high school diploma or equivalent, pass a background check, and complete specialized training provided by the hiring agency. Some positions may require prior law enforcement or security experience, and applicants often must pass written exams and physical assessments.

Is it hard to get into customs inspector?

Becoming a customs inspector typically requires passing written exams, background checks, and physical assessments. Candidates often need relevant education, such as a high school diploma or higher, and may need to complete training programs or obtain certifications. The hiring process can be competitive due to the specialized nature of the role and security clearance requirements.

What are popular job titles related to Customs Inspector jobs in Miami, FL?

For Customs Inspector jobs in Miami, FL, the most frequently searched job titles are:

What job categories do people searching Customs Inspector jobs in Miami, FL look for?

The top searched job categories for Customs Inspector jobs in Miami, FL are:

Customs Inspector jobs near you
Infographic showing various Customs Inspector job openings in Miami, FL as of August 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 100% Physical job distribution, with an average salary of $54,426 per year, or $26.2 per hour.

Assistant Manager, Quality Systems and Quality Assurance

ARKRAY

Doral, FL • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 24 days ago

Key responsibilities

  • Review and approve product labeling, FDA submissions, and manage regulatory activities related to medical devices.

  • Manage the Quality Management System, including supplier databases, validation programs, change control, and internal audits.

  • Oversee post-market surveillance activities such as customer complaints, product recalls, and MDR submissions to the FDA.

Job description

Summary
Ability and knowledge to conduct the work listed in at least one of the 5 major job Duties and Responsibilities(excluding General Duties), so that they contribute to company compliance with relevant laws and regulations.
Essential Responsibilities
Regulatory (Supporting Responsibility)
  • Actively engage in pre-/post-market regulatory activities, which include but are not limited to the following:
  1. Review and approval of product labeling.
  2. Review of FDA submissions.
  3. Assist/work with consultants as needed.
  4. Support R&D with 510(k) submissions.
  • Create Regulatory Master Plans for product launches.
  • Lead the development of new product labeling and oversee the labeling program to coordinate the review, approval, and tracking of all product labeling.
  • Act as the subject matter expert on UDI.GUDID regulations.
  • Manage FDA facility registrations and device listings.
  • Manage FDA import inspections, provide FDA data and information to US Customs, and work with both the FDA and US Customs to resolve shipments placed on hold.
  • Write Health Risk Assessments for Nonconforming products, customer complaints and MDRs.
  • Review ECRs.
  • Support Sales and Marketing to resolve any FDA compliance questions or concerns from customers.

Science (Supporting Responsibility)
  • Support Medical Lab Scientists of the Smart Assist project.
  • Support clinical studies as needed. Including but not limited to hands-on assistance in the clinical studies.
  • Train and support the Clinical Application Specialists and Field Service Engineers in their activities.
  • Perform other pre-/post-market activities as assigned.

Quality Assurance/Quality Management System (Primary Responsibility)
  • Manage the supplier databases for our major retail-chain partner.
  • Manage the Validation Program, Change Control Review, and approve Supplier Change Requests.
  • Coordinate the review, approval, and tracking of all Engineering Changes from our suppliers.
  • Review and approve ECRs.
  • Manage various Quality System databases.
  • Oversee software validations.
  • Fulfill the role of internal auditor. Also, manage the Internal Audit Program.
  • Prepare supplier audits and scorecards. Also, manage the Supplier Approval Program.
  • Conduct External Audits.
  • Assemble the monthly AOD presentation materials and present the training data.
  • Perform Quality Acceptance Inspections on products that are to be delivered to a 3rd-party logistics company and then perform the shipment permission inspection on products that are to be shipped from the 3rd-party logistics company.
  • Act as the Quality Plan Manager for Product Launches if required.
  • Ensure compliance with FDA QMSR, ISO 13485, and OSHA.
  • Fulfill the role of OSHA Safety Coordinator for our Miami Facility and any new facilities that may be added in the future.
  • Fulfill the role of CAPA Manager for CARs, SCARs, and ISCARs if required.
  • Chair the monthly AOD (Analysis of Data) meeting if required.
  • Prepare and present CAPA data at the monthly meeting if required.

Complaint Handling (Supporting Responsibility)
  • Oversees Post Market Surveillance - Customer Complaints.
  • Create the Monthly Risk Review Report.
  • Manage Product Recalls and other field actions.
  • Manage our Lab Division's Complaint Program and coordinate External Complaint with AFC (factory headquarters in Japan).
  • Chair the Lab Division's monthly Complaint Meeting.
  • Present the Lab Division's Complaints in the monthly AOD meeting.
  • Review Technical Bulletins.
  • Manage the Healthcare Division's Complaint Program.
  • Chair the Healthcare Division's monthly Complaint Meeting.
  • Present the Healthcare Division's Complaints in the monthly AOD meeting.
  • Submit MDRs to the FDA.
  • Create the Monthly Vendor Reporting.
  • Review the Daily Call Data of our major retail-chain partner.

General Duties
  • Act as the Facilities and Equipment Manager of our Miami location.
  • Pick up and process company mail.
  • Coordinate activities for the Miami Facility and Office.

This job description is not intended to be all-inclusive and the employee will also perform other reasonably related business duties as assigned by management.
Knowledge and Skills
  • Bachelor's Degree in chemistry, biology, engineering or other technical field required.
  • Two or more years of experience working in a regulated diagnostic industry required.
  • Senior roles will require seven or more years of experience working in a regulated diagnostic industry required.
  • Experience working with Class I and Class II medical devices, preferably laboratory, and Point of Care IVD instruments and reagents that are subject to US regulatory submission.
  • Knowledge and working experience on FDA, GMP/QSR, ISO, CFR and/or other regulatory issues related to medical devices.
  • Senior roles will require the ability to manage both undergoing ISO 13485 audits and conducting supplier audits in compliance with ISO 13485 standards.
  • Knowledge on US regulatory submissions. Ability to build direct relationships and deal with the FDA in relation to the submission process is preferred.
  • Clinical study management experience is preferred.
  • Experience in quality systems and quality assurance activities.
  • Proficiency in Microsoft Office programs (including, but not limited to Word, Adobe, Excel, PowerPoint)
  • Ability to travel.

Physical Requirements
Heavy keyboarding / PC use
ARKRAY is an Equal Opportunity Employer: minorities, women, veterans, and individuals with disabilities. ARKRAY offers a generous benefit package that includes Medical, Dental, Vision, 401K w/company match, FSA and HSA options.

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