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Costa Rica Medical Device Quality Jobs in Oregon

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Medical Device Assembler

Portland, OR · On-site

$20/hr

  • Medical

  • Dental

  • Vision

Perform quality checks and help identify and communicate quality issues that may impact production ... Medical Device Manufacturing, Medical Device Assembly, Production Operator, Medical Device ...

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Medical Device Assembler

Portland, OR · On-site

$18 - $20/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Come create your career with Volt Volt is immediately hiring a Medical Device Assembler in Portland ... Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ...

Quality Assurance Specialist, Sr

Newberg, OR · Remote

$86K - $119K/yr

Achieves and maintains deep technical understanding of ISO 13485, 21 CFR 820, EU MDR and other medical device quality management and regulatory compliance standards as applicable. * Other duties as ...

Quality Assurance Specialist, Sr

Newberg, OR · On-site

$86K - $119K/yr

Achieves and maintains deep technical understanding of ISO 13485, 21 CFR 820, EU MDR and other medical device quality management and regulatory compliance standards as applicable. * Other duties as ...

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ASSEMBLER - PA2025

Portland, OR · On-site

$20/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... quality medical devices in a manufacturing environment. This position will perform assembly, repair, and testing operations on medical device components, including pacemakers, implantable ...

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Quality Engineer

Portland, OR · On-site

$76K - $98K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

May collaborate with Regulatory on Medical Device Reporting (MDR) and adverse event reporting requirements * Coordinate planning, implementation and trending of multiple quality management systems ...

The Principal, Pharmacovigilance / Device Vigilance is a detail-oriented and proactive professional ... Partner with Clinical, Regulatory Affairs, Quality, and Medical Affairs teams * Support audits and ...

Medical Device & Diagnostics - CRA 2 - US Remote

OR · On-site +1

$105/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are currently seeking Experienced Device CRA 2s to lead and support our Medical Device ... quality issue. * Changing priorities constantly asking you to prioritize and adapt on the spot.

Accounting Manager

Hillsboro, OR

$138K - $195K/yr

  • Medical

  • Retirement

  • PTO

... United States, Costa Rica, Malaysia, and Vietnam. The Accounting Manager will oversee Intel ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Accounting Manager

Hillsboro, OR · On-site

$138K - $195K/yr

  • Medical

  • Retirement

  • PTO

... United States, Costa Rica, Malaysia, and Vietnam. The Accounting Manager will oversee Intel ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Knowledge of international standards and regulations (e.g., ISO 13485, MDSAP, FDA 21 CFR 820, CMDR SOR/98-282, Medical Device Directive 93/42/EEC, EU Medical Device Regulation 2017/745) and quality ...

Knowledge of international standards and regulations (e.g., ISO 13485, MDSAP, FDA 21 CFR 820, CMDR SOR/98-282, Medical Device Directive 93/42/EEC, EU Medical Device Regulation 2017/745) and quality ...

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Showing results 1-20

Costa Rica Medical Device Quality information

What are the key skills and qualifications needed to thrive in medical device quality roles in Costa Rica?

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 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 is a Costa Rica medical device quality job?

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.

What are popular job titles related to Costa Rica Medical Device Quality jobs in Oregon?

For Costa Rica Medical Device Quality jobs in Oregon, the most frequently searched job titles are:

Medical Device Assembler

Collaborative LLC

Portland, OR • On-site

$20/hr

Full-time

Medical, Dental, Vision

Posted yesterday

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Job description

Medical Device Production Operator / Assembler


Schedule: Primarily 2nd Shift — Monday-Thursday, 2:30 PM-1:00 AM OR Friday-Sunday, 6:00 AM-6:00 PM (36 hours worked, paid for 40 hours)
Industry: Medical Device Manufacturing


Job Summary

We are seeking a Medical Device Production Operator / Assembler to join a manufacturing team producing high-quality medical devices. Working under close supervision, this position performs a combination of assembly, repair, testing, and production operations involving pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.

The ideal candidate is detail-oriented, dependable, comfortable working with small components, and able to follow detailed written procedures and verbal instructions. This position offers the opportunity to work in a highly regulated medical device manufacturing environment while contributing to product quality, safety, and continuous improvement.


Key Responsibilities

  • Perform routine assembly, repair, testing, and production operations on medical device components and assemblies.
  • Assemble and handle small components and parts according to established procedures and manufacturing instructions.
  • Follow standardized work instructions, SOPs, verbal instructions, and other applicable manufacturing procedures.
  • Maintain accurate production records, travelers, and quality documentation to ensure product traceability.
  • Review and complete required job documentation and ensure manufacturing cell records remain accurate and up to date.
  • Perform quality checks and help identify and communicate quality issues that may impact production or finished products.
  • Utilize electronic data collection systems and computer software as required for production activities and documentation.
  • Follow all safety procedures and use appropriate safety equipment and devices during manufacturing operations.
  • Participate in continuous improvement and quality initiatives designed to improve production processes, quality, and efficiency.
  • Demonstrate a basic understanding of Lean Manufacturing principles and support efforts to improve cell performance.
  • Communicate production issues, ideas, concerns, and solutions clearly to manufacturing supervisors and management.
  • Prioritize work and determine the appropriate sequencing and timing of tasks based on production requirements.
  • Support Manufacturing Supervisors and Managers in monitoring individual and manufacturing cell performance metrics.
  • Maintain a positive and professional attitude when interacting with coworkers, management, internal customers, and visitors.
  • Support Quality Management Systems (QMS), Environmental Management Systems (EMS), and other applicable regulatory requirements.
  • Follow all applicable manufacturing, quality, environmental, and regulatory requirements.


Qualifications

  • High school diploma or equivalent required.
  • Ability to read, comprehend, and follow written procedures and work instructions.
  • Ability to understand and follow verbal instructions.
  • Strong attention to detail and commitment to producing high-quality work.
  • Ability to handle and maneuver small components and parts.
  • Basic computer skills and ability to utilize electronic data collection systems.
  • Ability to prioritize multiple tasks based on importance and production requirements.
  • Strong communication skills, both written and verbal.
  • Ability to make sound decisions and judgments with limited supervision.
  • Ability to work effectively in a team-oriented manufacturing environment.
  • Willingness to follow safety procedures, quality requirements, and standardized processes.


What You'll Do

You will play an important role in the production of life-saving medical devices, performing hands-on assembly, testing, repair, documentation, and quality-related activities. Attention to detail, following procedures, and maintaining accurate documentation are critical to ensuring every product meets stringent quality requirements.


Keywords: Medical Device Manufacturing, Medical Device Assembly, Production Operator, Medical Device Assembler, Assembly, Pacemakers, ICDs, Implantable Medical Devices, Testing, Repair, Quality Control, Quality Documentation, Manufacturing, Production, SOPs, Work Instructions, Traceability, Lean Manufacturing, QMS, EMS, Electronic Data Collection, Small Components, Continuous Improvement, Safety, Regulatory Compliance