ZipRecruiter

Log In

1

Medical Device Logistics Jobs in Boca Raton, FL (NOW HIRING)

previous page

Showing results 21-32

All JobsMedical Device Logistics JobsMedical Device Logistics Jobs in Boca Raton, FL

Medical Device Logistics information

See Boca Raton, FL salary details

$37.5K

$62.1K

$82.1K

How much do medical device logistics jobs pay per year?

As of Aug 6, 2026, the average yearly pay for medical device logistics in Boca Raton, FL is $62,068.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,500.00 and $68,800.00 per year, depending on experience, location, and employer.

What is medical device logistics?

Medical device logistics refers to the management and coordination of the storage, transportation, and distribution of medical devices from manufacturers to healthcare providers or end users. This process ensures that medical equipment and supplies are delivered safely, efficiently, and in compliance with regulatory standards. Effective medical device logistics also includes inventory management, tracking, and quality control to maintain device integrity and availability. Professionals in this field work to minimize delays, prevent damage, and ensure devices reach their destination in optimal condition.

What are the key skills and qualifications needed to thrive in medical device logistics, and why are they important?

To thrive in Medical Device Logistics, you need expertise in supply chain management, inventory control, regulatory compliance, and a relevant degree or certification like APICS or CSCP. Familiarity with ERP systems, inventory tracking software, and understanding of FDA or ISO regulations are typically required. Strong attention to detail, problem-solving abilities, and effective communication skills help professionals excel in coordinating with vendors and healthcare providers. These skills ensure the safe, timely, and compliant delivery of critical medical devices, directly impacting patient care and operational efficiency.

What are some common challenges faced in medical device logistics, and how can I prepare for them?

Professionals in Medical Device Logistics often encounter challenges such as managing strict regulatory compliance, ensuring timely delivery of sensitive equipment, and coordinating across multiple departments or external partners. Being detail-oriented, adaptable, and proactive in problem-solving can help you address these issues effectively. Familiarizing yourself with relevant regulations, learning about inventory management systems, and building strong communication skills will also prepare you for success in this role.

What is the difference between Medical Device Logistics vs Medical Equipment Technician?

AspectMedical Device LogisticsMedical Equipment Technician
CredentialsLogistics certifications, supply chain trainingTechnical certifications, biomedical equipment training
Work EnvironmentWarehouses, distribution centers, hospitalsHospitals, clinics, repair facilities
Employer & IndustryMedical device companies, healthcare providersHospitals, medical equipment service companies

Medical Device Logistics focuses on managing the supply chain, inventory, and distribution of medical devices, ensuring timely delivery. Medical Equipment Technicians repair, maintain, and calibrate medical equipment. While both roles support healthcare, logistics centers on supply chain management, whereas technicians handle equipment functionality and safety.

What job categories do people searching Medical Device Logistics jobs in Boca Raton, FL look for? The top searched job categories for Medical Device Logistics jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Medical Device Logistics jobs? Cities near Boca Raton, FL with the most Medical Device Logistics job openings:
Medical Device Logistics jobs near you
Infographic showing various Medical Device Logistics job openings in Boca Raton, FL as of July 2026, with employment types broken down into 75% Full Time, 18% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $62,068 per year, or $29.8 per hour.

Supervisor, Quality Control (TAS)

Terumo Corporation

Sunrise, FL • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 hours ago

Job description

At Terumo Aortic, our mission is to transform the treatment of aortic disease worldwide. With our comprehensive portfolio of surgical, endovascular and hybrid technologies, we enable physicians to find the right fit for each patient anatomy.

The company has over 1,250 associates around the world with manufacturing facilities in Glasgow, Scotland and Sunrise, Florida.

Terumo Aortic is focused on the continuing development of new and innovative products driving the growth of the business globally. Associates are part of a stimulating and exciting environment in which they can develop their skills and achieve career goals. Working for the company, each associate's role contributes greatly to helping to save or improve the lives of patients in over 100 countries worldwide.

At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat - progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, impactful solutions for patients.

Join us and help shape wherever we go next!

Advancing healthcare with heart

www.terumoaortic.com

Job Summary

Provides technical, clerical, and logistical support to the Quality Operations program. Supervises inspectors in Quality Control Operations Areas to ensure continuous workflow and appropriate use of sampling plans and tools, as applicable. Works with other departments on the development and execution of equipment and / or test method validations. Analyzes and investigates non-conformities, and triggers CAPA escalations as needed.

Job Details/Responsibilities
  • Supervises a team of several inspectors in the Quality Control Operation Areas.
  • Must be able to analyze trends and recommend appropriate changes to sampling plans, procedures, inspections methods, or tooling.
  • Recommends modifications / improvement where advisable to minimize cost and labor.
  • Coordinates and participates in audits whether that be internal or external to ensure quality compliance.
  • Must be able to evaluate and implement changes for efficiency and effectiveness of inspections.
  • Analyzes and investigates both in house and field data, reports quality problems, recommends corrective action, and follows up on the implementation and effectiveness of solutions.
  • Assure responsibilities are carried out in compliance with applicable quality systems (i.e.ISO13485, 21CFR820).
  • Interface with Research and Development and other engineering departments to determine if process or product changes are needed based on NCR investigations.
  • Requests and confirms corrections, corrective actions, and/or preventive actions from suppliers, engineers (as needed) to ensure that non-conformances are properly corrected, and recurrence is prevented.
  • Updates Quality procedures/documents as needed to ensure efficient workflow and appropriate use of equipment/tools, and sampling plans.
  • Facilitates inspector training and ensures relevant training requirements are up to date.
  • Manages non-conformance report generation, tracking and closure.
Job Responsibilities (continued)

Quality requirements: 

  • Ensure compliance with all quality systems regulatory requirements such as, but not limited to, ISO 13485, 21 CFR Part 820, MDSAP, MDD (93/42/EEC) and MDR (EU 2017/745)
  • Responsible for addressing issues within the QMS without undue delay as evidenced by on time completion of actions on the Single Action Tracker (SAT)

EH&S Requirements: 

  • Ensure compliance with all quality systems regulatory requirements such as, but not limited to, ISO 13485, 21 CFR Part 820, MDSAP, MDD (93/42/EEC) and MDR (EU 2017/745).
  • Responsible for addressing issues within the QMS without undue delay as evidenced by on time completion of actions on the Single Action Tracker (SAT).
  • Provide recourse to meet Environmental Health and Safety goals.
  • Maintain defined organisation Environmental Health and Safety competencies.
  • Ensure related Risk Assessments are completed, accidents raised and action hazards
Knowledge, Skills and Abilities (KSA)
  • Excellent Written and Verbal Communication
  • Understanding of quality system regulations (ISO13485, 21CFR820)
  • Ability to interact with all levels within organization.
  • Analytical skills for compiling and analyzing data.
  • Knowledge of sampling plans
  • Computer and software skills 
  • Ability to motivate others and improve efficiency.
Qualifications/ Background Experiences
  • BS in Engineering or more than 5 years in the Medical Device industry with more than 5 years of experience in the quality field.
  • Familiarity with management of non-conforming product.
  • Familiarity with sampling plans, and failure analysis investigations.

It is Terumo's policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment.

Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program. Salary - $72,000 to 100,000

Apply