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Costa Rica Medical Device Quality Jobs (NOW HIRING)

Kellton Tech

Medical Device Quality Inspector

Madison, WI · On-site

$25 - $30/hr

Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $25-30/hr. on W2 **Opportunity to earn overtime pay** The Medical Device Quality Inspection group is responsible for assuring ...

Kellton Tech

Medical Device Quality Engineer

Madison, WI · On-site

$40 - $45/hr

Medical Device Quality Engineer Location: Madison, WI Pay Rate : $40--45/hr on W2 Schedule: Onsite, Monday-Friday (standard business hours) Summary The Senior Quality Analyst/Engineer is responsible ...

medplast

Process Engineer

San Antonio, TX

About the company: Viant is a global medical device partner providing design, development ... Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana ...

medplast

Process Engineer

San Antonio, TX

About the company: Viant is a global medical device partner providing design, development ... Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana ...

medplast

Process Engineer

San Antonio, TX · On-site

About the company: Viant is a global medical device partner providing design, development ... Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana ...

Viant

Process Engineer

San Antonio, TX · On-site

S., Costa Rica, Tijuana, and Vega Baja, PR) Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life ...

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Costa Rica Medical Device Quality information

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

As of Jul 22, 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 July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, 2% Temporary, and 1% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $76,384 per year, or $36.7 per hour.

Medical Device Quality Inspector

Kellton Tech

Madison, WI • On-site

$25 - $30/hr

Contractor

Posted 27 days ago

Job description

Job Title: Medical Device Quality Inspector
Location: Madison, WI (Onsite)
Pay Rate: $25-30/hr. on W2

**Opportunity to earn overtime pay**

The Medical Device Quality Inspection group is responsible for assuring that materials, activities, processes, and specified conditions related to the daily device manufacturing, processing, and packaging meet current GMP standards and comply with applicable procedures and standards such as to ensure the quality integrity of the product.

Primary Responsibilities

  • The Medical Device Quality Inspector inspects parts to specifications that are on a part drawing.
  • Perform part inspections using measurement tools such as calipers, micrometers, gage pins, plug gages, and thread gages
  • This person would also be trained to an ERP system; SAP to enter in acceptance data.
  • Use of another system related to nonconforming material reports to enter failure data.
  • Material inspection experience as described and be able to work with computer-based applications.
  • Follow procedures to adhere to industry and regulatory standards.
  • Team collaboration in supporting production, which means being flexible on assignments
  • Work overtime is desired as needed, to support production schedules and incoming part volumes.

Required and preferred qualifications

  • High School diploma. College Degree preferred
  • Good written and verbal communication skills. Basic math skills
  • Ability to use measurement devices such as calipers, thread gauges and micrometers to check whether materials or products meet standards
  • Familiar with ISO13485 or ISO 9001 desired
  • Experience with optical measurement machines or a CMM desired
  • Attention to detail with ability to identify defects and flaws
  • Ability to work in a fast-paced team environment with minimal supervision
  • Use of Microsoft Word and Excel.
  • SAP desired. Will train otherwise