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Costa Rica Medical Device Quality Jobs (NOW HIRING)

Saxon Global

QA ENGINEER

Saint Augustine, FL · On-site

Medical Device Quality Engineer Position Type :Contract Projected Start Date :08-09-2017 Zip Code :33716 City :St. Petersburg State :FL Required Skills : ISO 9000 Not looking for a Design or testing ...

ATL Technology

Quality Engineer II/III

Maple Grove, MN · On-site

$73K - $95K/yr

Quality Engineer II/III The Quality Engineer with have a great aptitude for learning, being ... top medical device manufacturers. ATL has operations in China, Costa Rica, Taiwan, UT-USA, plus ...

Establishment Labs

Warranty Specialist

Austin, TX · On-site

About Us: Establishment Labs is changing the medical device, breast health, aesthetics and ... Costa Rica and are approved for sale in more than 85 countries. Since 2018 the company trades on ...

Heartflow

Senior Device Quality Engineer

San Francisco, CA · Hybrid

$160K - $180K/yr

You will bridge the gap between rapid Agile development and rigorous medical device regulations ... Design Quality & Risk Management * Design Reviews: Participate in software architecture reviews to ...

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Costa Rica Medical Device Quality information

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$70

How much do costa rica medical device quality jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for costa rica medical device quality in the United States is $36.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $45.91 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Quality roles in Costa Rica, and why are they important?

To thrive in a Medical Device Quality role in Costa Rica, you need a solid understanding of quality management systems, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and experience in medical device manufacturing. Familiarity with quality assurance tools, document control systems, and certifications like Six Sigma or ASQ Certified Quality Engineer are typically required. Strong attention to detail, analytical thinking, and effective teamwork and communication skills help individuals excel in this field. These competencies ensure products meet rigorous safety and regulatory standards, supporting both patient safety and company reputation.

What are some common challenges faced by professionals working in medical device quality roles in Costa Rica, and how can they be addressed?

Professionals in medical device quality roles in Costa Rica often face challenges related to navigating both local and international regulatory requirements, ensuring consistent product quality, and adapting to frequent updates in compliance standards. Effective communication and collaboration with cross-functional teams—such as engineering, production, and regulatory affairs—are crucial for addressing these challenges. Staying updated with global quality standards, participating in regular training, and utilizing robust quality management systems can help professionals maintain compliance and drive continuous improvement.

What is the difference between Costa Rica Medical Device Quality vs Costa Rica Medical Device Regulatory Affairs Specialist?

AspectCosta Rica Medical Device QualityCosta Rica Medical Device Regulatory Affairs Specialist
CertificationsISO 13485, internal quality auditsRegulatory compliance, local and international approvals
Work EnvironmentManufacturing sites, quality control labsRegulatory agencies, documentation review
Industry UsageQuality assurance, process improvementRegulatory submissions, compliance management

While both roles focus on ensuring medical device safety and compliance, Costa Rica Medical Device Quality primarily emphasizes quality assurance and process control within manufacturing. In contrast, Costa Rica Medical Device Regulatory Affairs Specialists handle regulatory submissions and ensure compliance with local and international regulations. Both roles are essential in the medical device industry but differ in their core responsibilities and daily tasks.

What are Costa Rica Medical Device Quality jobs?

Costa Rica Medical Device Quality jobs involve ensuring that medical devices manufactured or distributed in Costa Rica meet local and international quality standards and regulatory requirements. Professionals in these roles oversee quality assurance processes, conduct audits, manage compliance documentation, and collaborate with engineering and production teams to maintain product safety and effectiveness. These positions are crucial in the country's growing medical device sector, which is known for its adherence to strict quality and regulatory standards.
More about Costa Rica Medical Device Quality jobs
What cities are hiring for Costa Rica Medical Device Quality jobs? Cities with the most Costa Rica Medical Device Quality job openings:
What states have the most Costa Rica Medical Device Quality jobs? States with the most job openings for Costa Rica Medical Device Quality jobs include:
What job categories do people searching Costa Rica Medical Device Quality jobs look for? The top searched job categories for Costa Rica Medical Device Quality jobs are:
Costa Rica Medical Device Quality jobs near you
Infographic showing various Costa Rica Medical Device Quality job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 86% Full Time, and 13% Part Time. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $76,384 per year, or $36.7 per hour.
QA ENGINEER

QA ENGINEER

Saxon Global

Saint Augustine, FL • On-site

Full-time

Posted 14 days ago

Job description

Company Description

Saxon Global is one of the fastest growing Inc 500 Companies in the US, providing enhanced IT consulting, and engineering solution services.

Job Description

Job Title :Medical Device Quality Engineer

Position Type :Contract

Projected Start Date :08-09-2017

Zip Code :33716

City :St. Petersburg

State :FL

JOB DESCRIPTION

Required Skills :

ISO 9000
Not looking for a Design or testing engineer. This person will NOT be doing and design or testing.
medical device required.

Basic Qualifications :

Additional Skills :

Job Description :

Apex Systems has a long-term contract opening for a Medical Device Quality Engineer / Compliance Engineer with a large manufacturing services organization in St. Petersburg, FL. Client is looking for someone with a background working in a Medical Device Design environment.

Client Job Description:

Job Summary - Design Quality Engineer

Essential Duties & Responsibilities

Qualifications

XYZ

Additional Information

All your information will be kept confidential according to EEO guidelines.

Saxon global logo

About Saxon global

Sourced by ZipRecruiter

Saxon Global is a leading IT consulting and staffing company based in Irving, Texas. The company operates in the technology services industry and has been providing unparalleled services to its clients for over a decade. Saxon Global specializes in app development, business intelligence (BI), and data integration services. Established in 2007, the company was founded on the principle of harnessing the power of data and technology to drive business success. With their focus on innovation, quality, and superior service, Saxon Global aims to help businesses achieve their goals with significantly increased efficiency and effectiveness.

Industry

Recruiting and staffing services

Company size

201 - 500 Employees

Headquarters location

Irving, TX, US

Year founded

2000

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