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Import Logistics Manager Jobs in Raleigh, NC (NOW HIRING)

Director of Quality US

Raleigh, NC · On-site

$110K - $130K/yr

Maintain and develop the company's Quality Management System to support third party logistics ... Ensure products are only imported from authorized sites and meet all local quality requirements ...

Learning & Development Corporate Intern

Raleigh, NC · On-site

$13.50 - $18/hr

... Management System. * Import, assign and track records for training classes. * Support the coordination and logistics of training sessions, including scheduling, communication, and tracking attendance.

Learning & Development Corporate Intern

Raleigh, NC · On-site

$13.50 - $18/hr

... Management System. * Import, assign and track records for training classes. * Support the coordination and logistics of training sessions, including scheduling, communication, and tracking attendance.

Learning & Development Corporate Intern

Raleigh, NC · On-site

$13.50 - $18/hr

... Management System. * Import, assign and track records for training classes. * Support the coordination and logistics of training sessions, including scheduling, communication, and tracking attendance.

Showing results 21-34

Import Logistics Manager information

See Raleigh, NC salary details

$33.5K

$74.2K

$127.8K

How much do import logistics manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for import logistics manager in Raleigh, NC is $74,166.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,900.00 and $88,000.00 per year, depending on experience, location, and employer.

What is an import logistics manager?

An Import Logistics Manager is a professional responsible for overseeing and coordinating the transportation, customs clearance, and delivery of goods coming into a country. They manage relationships with suppliers, freight forwarders, and customs brokers to ensure shipments arrive on time and comply with all regulations. Their role includes tracking shipments, resolving delays, managing documentation, and optimizing logistics processes to reduce costs and improve efficiency.

What are the key skills and qualifications needed to thrive as an import logistics manager?

To thrive as an Import Logistics Manager, you need expertise in supply chain management, international trade regulations, and logistics coordination, typically supported by a bachelor's degree in business, logistics, or a related field. Familiarity with ERP systems, transportation management software, and customs documentation processes is essential. Strong organizational skills, attention to detail, and effective communication help manage complex shipments and vendor relationships. These skills ensure timely, cost-effective, and compliant import operations in a global business environment.

What are some typical challenges faced by import logistics managers and how can they be addressed?

Import Logistics Managers often encounter challenges such as navigating complex international regulations, coordinating with multiple vendors across different time zones, and managing unexpected shipping delays. Staying up-to-date with changes in customs requirements and developing strong relationships with reliable freight forwarders are key strategies for success. Proactive communication and robust tracking systems also help minimize disruptions, ensuring shipments arrive on schedule and within budget.

What is the difference between Import Logistics Manager vs Import Coordinator?

AspectImport Logistics ManagerImport Coordinator
CredentialsTypically requires a bachelor’s degree in logistics, supply chain, or related field; certifications like CCLP or CSCP are commonOften requires a high school diploma or associate degree; some roles prefer certifications like CCLP
Work EnvironmentOversees entire import operations, manages teams, and coordinates with multiple departmentsFocuses on processing shipments, documentation, and communication with carriers and customs
Employer & Industry UsageUsed in large logistics companies, import/export firms, and manufacturing industriesCommon in freight forwarding companies, customs brokerage, and import departments

The Import Logistics Manager has a broader, strategic role overseeing import operations, while the Import Coordinator handles day-to-day shipment processing and documentation. Both roles are essential in the import supply chain but differ in scope and responsibilities.

What are the most commonly searched types of Import Logistics jobs in Raleigh, NC?

The most popular types of Import Logistics jobs in Raleigh, NC are:

What are popular job titles related to Import Logistics Manager jobs in Raleigh, NC?

For Import Logistics Manager jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Import Logistics Manager jobs in Raleigh, NC look for?

The top searched job categories for Import Logistics Manager jobs in Raleigh, NC are:

Infographic showing various Import Logistics Manager job openings in Raleigh, NC as of July 2026, with employment types broken down into 86% Full Time, 10% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $74,166 per year, or $35.7 per hour.

Director of Quality US

Euromed Pharma Us Inc

Raleigh, NC • On-site

$110K - $130K/yr

Full-time

Re-posted 29 days ago


Job description

About the Role:
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and champion quality assurance initiatives. This is a high-impact leadership role where you'll shape the quality culture of a growing pharmaceutical organization. If you're passionate about compliance & regulatory, excellence, and making a difference in the pharma industry, we want to hear from you.
Key Responsibilities:

1. Quality Assurance & QMS Oversight
  • Maintain and develop the company’s Quality Management System to support third party logistics activities in compliance with all state, federal and international regulations as applicable 
  • Own and manage key QMS processes, including CAPA, Change Control, Deviations, Complaints, Document Control, Data Integrity, Recalls and Internal Audits 
  • Lead Management Reviews and promote a culture of continuous improvement 
  • Ensure alignment between quality processes and operational functions, including warehousing, logistics, and commercial supply chain activities 
  • Provide input into strategic business initiatives, driving process efficiency and compliance 
  • Serve as the primary point of contact for regulatory inspections, audits, and agency communications
  • Represent the company during regulatory inspections (Authority and customer audits 
2. Responsible Person (RP)
  • Ensure compliance with FDA, cGDP requirements  and applicable regulations for wholesale distribution acting as Responsible Person
  • Maintain compliance with the Drug Supply Chain Security Act (DSCSA), including serialization, verification, and transaction documentation 
  • Maintain and approve supplier and customer bona fides; ensure all third-party licenses are verified and current 
  • Oversee recall, returns, complaints, and falsified product investigations 
  • Approve training programs and verify competence of all staff involved in distribution activities
  • Authorize return to saleable stock decisions and oversee product storage, temperature excursions, and transport records 
  • Approve contracts and SOPs related to distribution and outsourced activities 
  • Ensure records for the minimum period required by the law 
  • Participate in senior-level decisions relating to quarantine, disposal, or recall of medicines 
  • Fulfil the obligations required for importation of medicinal products 
  • Ensure products are only imported from authorized sites and meet all local quality requirements before release 
  • Verify that products imported under the WDA(H) are fully compliant 
  • Work closely with supply chain partners and import/export authorities to ensure compliance at all touchpoints 
  • Represent the company during FDA, customer, and state inspections
Additional Responsiblities
  • Maintain inspection readiness at all times across facilities and systems
  • Ensure full compliance with internal policies, including Health & Safety, Pharmacovigilance, Falsified Medicines legislation and corporate governance
  • Safeguard company reputation by promoting ethical, compliant, and customer focused business practices
  • Provide training, mentorship, and leadership to quality and operational staff 
  • Perform delegated duties in the absence of colleagues where appropriate
  • Other duties which may be reasonably required from time to time by company managers, including delegated duties during the absence of colleague.
Requirements:
  • Bachelor's degree or higher in Pharmacy, Life Sciences, Chemistry, or a related field
  • 7+ years of quality assurance experience in the pharmaceutical industry
  • Familiarity with federal and state regulatory frameworks (e.g. FDA, DSCSA, State Boards of Pharmacy) Preferred: completion of certified training in Good Distribution Practice
  • Strong understanding of US, EU, UK and international regulatory frameworks (e.g. FDA, EMA, MHRA)
  • Auditing experience (internal and external) of suppliers, vendors, and contractors
  • Familiarity with ISO9001 QMS and Controlled Drug regulations (US DEA)
  • Knowledge of US Customs and Border Protection requirements
  • Knowledge of COSHH and hazardous goods transportation
  • Excellent interpersonal, written and verbal communication skills
  • Strong leadership, communication, and cross-functional collaboration skills
  • Team oriented with leadership, training, and delegation capabilities
  • Customer focused, innovative, and process-improvement minded
  • Detail-oriented, decisive, and committed to a culture of continuous improvement
About Us:
Euromed Pharma US Inc is part of the 60-year strong Petrone Group, dedicated to delivering high-quality, innovative healthcare and pharmaceutical solutions globally. Our team is driven by a shared commitment to patient safety, regulatory excellence, and scientific integrity. We offer a collaborative and forward-thinking work environment where talented professionals can grow and make a meaningful impact in the pharmaceutical industry.