ZipRecruiter

Log In

1

Costa Rica Medical Device Quality Jobs (NOW HIRING)

Boston Scientific

Senior Quality Specialist

Arden Hills, MN · Hybrid

$86K - $119K/yr

Costa Rica-Coyol; Costa Rica-Heredia; US-MA-Marlborough; US-MN-Arden Hills; US-MN-Maple Grove ... Strong understanding of medical device Quality System directives, regulations, and standards.

Boston Scientific

Senior Quality Specialist

Arden Hills, MN · Hybrid

$83K - $114K/yr

Costa Rica-Coyol; Costa Rica-Heredia; US-MA-Marlborough; US-MN-Arden Hills; US-MN-Maple Grove ... Strong understanding of medical device Quality System directives, regulations, and standards.

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 ...

Viant Medical

Director of Supply Chain

Tempe, AZ

$176K - $200K/yr

About the company: Viant is a global medical device partner providing design, development ... Costa Rica; Tijuana, BC; and Vega Baja, PR sites. What you will'do: Systems: Establish and optimize ...

next page

Showing results 1-20

All JobsCosta Rica Medical Device Quality Jobs

Costa Rica Medical Device Quality information

See salary details

$21

$36

$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.

Senior Coding Specialist- Costa Rica (Home Based)

Fortrea

San Jose, CA • On-site, Remote

Full-time

Posted 3 days ago

Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

45th of 57 rated research

Job description

Senior Coding Specialist

📍 Costa Rica
Candidates must be based in Costa Rica

Are you passionate about medical coding quality and clinical data integrity? We're looking for a Senior Coding Specialist based in Costa Rica to support highquality, compliant clinical trial data across global studies.

What you'll do
  • Review and ensure the quality and consistency of medical coded data delivered by external vendors
  • Provide oversight of outsourced coding activities, including dictionary and synonym reviews
  • Support MedDRA and WHO Drug Dictionary upversioning across multiple studies
  • Act as a subject matter expert for dictionary usage and coding quality
  • Identify and escalate coding-related issues, proposing clear and practical solutions
  • Ensure compliance with ICH/GCP, regulatory requirements, and industry best practices
What you bring
  • Degree in Life Sciences, Health-related field, or equivalent experience
  • Fluent English (written and spoken)
  • 5+ years of experience in medical coding using MedDRA and WHO Drug Dictionaries
  • Experience in a CRO, pharmaceutical, or biotechnology environment
  • Strong attention to detail, ability to manage priorities, and a collaborative mindset
  • Experience with coding tools (e.g., Veeva, Medidata RAVE Coder) is a plus
Why join us
  • Work on global, highimpact clinical research studies
  • Be recognized as a medical coding and dictionary expert
  • Collaborate with experienced, international teams
  • Grow your career in Clinical Data Management

👉 Important: This position is based in Costa Rica, and applications will only be considered from candidates currently located in Costa Rica.

Learn more about our EEO & Accommodations request here.

Apply