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Costa Rica Medical Device Quality Jobs (NOW HIRING)

medplast

Weld Operator

Fort Wayne, IN

$800/wk

Leader in Medical Device Industry! 3rd Shift - Weld Operator 15% Shift Premium Pay based on ... S. and around the world, including low-cost facilities in Costa Rica, China, Mexico, and Puerto ...

New

medplast

Weld Operator

Fort Wayne, IN

$800/wk

Leader in Medical Device Industry! 3rd Shift - Weld Operator 15% Shift Premium Pay based on ... S. and around the world, including low-cost facilities in Costa Rica, China, Mexico, and Puerto ...

New

medplast

Weld Operator

Fort Wayne, IN

$800/wk

Leader in Medical Device Industry! 3rd Shift - Weld Operator 15% Shift Premium Pay based on ... S. and around the world, including low-cost facilities in Costa Rica, China, Mexico, and Puerto ...

New

GSK

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

Ensure compliance with relevant FDA, ISO, EU MDR, global, and GSK requirements for medical devices ... Act as site Subject Matter Expert (SME) for device quality processes, providing guidance to ...

Flotec

Be Seen First

Quality Engineer

Avon, IN · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Manufacturing Company Overview Flotec is an Indianapolis-based medical device manufacturer specializing in respiratory and oxygen delivery equipment. We manufacture ...

Excel Medical Products

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Document production activities, lot traceability, and quality records per FDA and ISO regulations ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Resonetics

Operator II VS4 Days

Hutchinson, MN

$19.50 - $21/hr

High School Diploma or Equivalent or completion of primary school in Costa Rica * Minimum three ... Familiarity with ISO Quality Systems particularly in medical device manufacturing. * Use of optical ...

Excel Medical Products

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Document production activities, lot traceability, and quality records per FDA and ISO regulations ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Excel Medical Products

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Document production activities, lot traceability, and quality records per FDA and ISO regulations ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Resonetics

Operator II VS4 Days

Hutchinson, MN

$19.50 - $21/hr

High School Diploma or Equivalent or completion of primary school in Costa Rica * Minimum three ... Familiarity with ISO Quality Systems particularly in medical device manufacturing. * Use of optical ...

Biogen

Senior Device Quality Engineering Lead

Cambridge, MA · Hybrid

$138K - $185K/yr

As the Senior Device Quality Engineering Lead, you will hold a pivotal role in ensuring the quality ... This senior-level position requires you to work closely with device development teams, medical ...

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All JobsCosta Rica Medical Device Quality Jobs

Costa Rica Medical Device Quality information

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$21

$36

$70

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

As of Jul 24, 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.
Industrial Engineer, Senior Staff

Industrial Engineer, Senior Staff

Confluent Medical Technologies

Austin, TX

$90K - $123K/yr

Full-time

Posted 11 days ago

Job description

Job Description:

Senior Staff Process Development Engineer - Manufacturing Systems (Austin, TX)

Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapidprototypethrough high-volume production. Our unparalleled technicalexpertise, proven experience, and deep partnership with our clients allow us to deliver world-class medical devices through innovative materials science, engineering, and manufacturing. Our primary capabilities include Nitinol components, balloon expandable stents and catheters, delivery systems, biomedical textiles, access kits, and guidewires. This role strengthens the manufacturing system architecture that enables predictable, scalable execution.

We take pride in being a leader in the medical technology space and are driven by a passion to create products that enable next-generation minimallyinvasiveprocedures.

Position Summary

This role focuses on manufacturing line design, process flow, capacity modeling, and scalability. The Senior Process Development Engineer - Manufacturing Systems owns end-to-end manufacturing line architecture, performance, and scalability. This role defines how processes flow, scale, and validate across production lines while partnering with Automation Engineering, who own custom equipment design and detailed machine controls.

Key Responsibilities

Manufacturing Line Design & Flow: Design end-to-end process flows, line layouts, takt models, and WIP strategies.

Industrial Engineering & Scaling: Perform capacity analysis, bottleneck identification, and staffing optimization.

Systems Integration: Integrate manual and automated steps into cohesive lines; define high level equipment specifications, placement and line interfaces in partnership with automation partners.

Risk, Data & Validation Support: Support PFMEA from a manufacturing system perspective; ensure line readiness for IQ/OQ/PQ.

Cross-Site Deployment: Support Costa Rica transfers, ramp planning, and manufacturing readiness.

Validation & Documentation

  • Lead process characterization, DOE studies, and statistical validation activity.
  • Generate line-level engineering documentation including work instructions, inspection procedures, protocols, and reports.
  • Design and execute process validation protocols (IQ/OQ/PQ) from a line and system readiness perspective.
  • Contribute to PFMEAs and risk analyses.

Cross-Site Collaboration & Leadership

  • Provide technical leadership for line development initiatives supporting catheter manufacturing.
  • Support transfersto Costa Ricaby coordinating installation, debug, validation, and training.
  • Mentor junior engineers andprovidetechnical guidance to technicians (without direct managerial responsibility).
  • Support standardization of production lines, equipment interfaces, and validation approaches across sites.

Education & Experience

  • Bachelor's degree in Mechanical, Industrial, Manufacturing Engineering, or related field.
  • 9-12 years of experience in manufacturing systems, industrial engineering, or process development within regulated environments.
  • Demonstrated experience scaling complex, small-scale assembly processes into stable, high-volume production lines.
  • Experience defining line architecture, equipment requirements, staffing models, and capacity plans in collaboration with automation and operations teams.
  • Proficiencyin SolidWorks (models, assemblies, drawings)
  • Minitab experience a plus.
  • Familiarity with materials used in catheter assemblies.
  • Experience inMedical device industry or other highly regulated manufacturing environment.
  • Demonstrated experience in processcharacterization,validation, and control(DOE,IQ/OQ/PQ, SPC)
  • Green or Black Belt certificationa plus.
  • Demonstrated ability to lead cross-functional engineering efforts and influence technical direction

Work Environment & Physical Requirements

  • Work performed in office, engineering lab, and Class 8 cleanroom environments.
  • Ability tolift upto 50 lbs.
  • Ability to standatdevelopment benches or workstations for extended periods.
  • Occasional cleanroom gowningrequired.
  • Travel up to 50%, primarily to Costa Rica, condensed around critical project phases (not continuous).

Additional Information

We regret that we are unable to sponsor employment visas or consider individuals on timelimited visa status for this position.
Confluent Medical Technologies is an Equal Opportunity Employer.
Only qualified candidates will be contacted.

Apply