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Costa Rica Medical Device Quality Jobs in Oregon

A-dec, Inc.

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 ...

A-dec, Inc.

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 ...

Intel

Accounting Manager

Hillsboro, OR · On-site

$138K - $195K/yr

... 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 ...

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research ... Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745 ...

A-dec, Inc.

Manager, Quality Assurance

Newberg, OR · On-site

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 ...

A-dec, Inc.

Manager, Quality Assurance

Newberg, OR · On-site

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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Costa Rica Medical Device Quality information

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 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 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:

What job categories do people searching Costa Rica Medical Device Quality jobs in Oregon look for?

The top searched job categories for Costa Rica Medical Device Quality jobs in Oregon are:

Costa Rica Medical Device Quality jobs near you

Medical Device Sales Representative

Hughes Surgical

Eugene, OR • On-site

Other

Posted yesterday

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Job description

Company Description Hughes Surgical is a medical device company focused on providing high-quality products and solutions to healthcare professionals and surgical teams. The organization works closely with hospitals, clinics, and specialty practices to support better patient outcomes and efficient surgical workflows. Hughes Surgical emphasizes strong clinical partnerships, reliable product performance, and responsive customer support. Team members collaborate with medical professionals in a dynamic environment that values integrity, service, and continuous improvement.

Role Description This is a remote, contract role for a Medical Device Sales Representative. The individual in this role will be responsible for identifying and developing new business opportunities, managing existing accounts, and driving sales of medical devices to healthcare providers and facilities. Day-to-day activities include scheduling and conducting virtual and on-site meetings with surgeons, nurses, and purchasing teams; presenting product features and benefits; providing product demonstrations and in-servicing; and supporting the adoption and proper use of devices. The role involves working closely with operating room staff and orthopedic specialists, responding promptly to inquiries, coordinating product trials, and ensuring timely follow-up. The representative will maintain accurate records in CRM systems, monitor territory performance, and collaborate with internal teams to address customer needs and support product launches.

Qualifications

  • Strong Medical Sales and general Sales skills, with a track record of achieving or exceeding sales targets.
  • Knowledge of Orthopedics and the Operating Room environment, including familiarity with surgical workflows and protocols.
  • Understanding of Medicine and clinical terminology to communicate effectively with healthcare professionals.
  • Excellent communication, presentation, and negotiation skills, with the ability to build long-term professional relationships.
  • Self-motivated, organized, and able to work independently in a remote, contract capacity.
  • Experience working with medical devices or in healthcare-related sales is strongly preferred.
  • Proficiency with CRM tools and basic office software for managing accounts, schedules, and documentation.
  • Bachelor’s degree in a relevant field (e.g., Life Sciences, Business, or related discipline) or equivalent professional experience.
  • Willingness to travel within an assigned territory as needed for on-site visits, trainings, and meetings.

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