1

Costa Rica Medical Device Quality Jobs in Oregon

Be Seen First

Production Operator - Manufacturing

Newberg, OR · On-site

$17.50 - $21.25/hr

This is a relatively new venture founded by medical device industry veterans and is a small but rapidly growing operation. Join our hard-working & dedicated team onsite to ensure the highest quality ...

Be Seen First

Production Operator - Manufacturing

Newberg, OR

$17.50 - $21.25/hr

This is a relatively new venture founded by medical device industry veterans and is a small but rapidly growing operation. Join our hard-working & dedicated team onsite to ensure the highest quality ...

Software Engineer

Lake Oswego, OR · On-site

$100 - $125/hr

We are a pioneer in developing innovative implantable medical device technologies and devices that save and enhance the quality of life for millions of individuals living with cardiovascular and ...

We are a pioneer in developing innovative implantable medical device technologies and devices that save and enhance the quality of life for millions of individuals living with cardiovascular and ...

Staff IC Design Engineer, Analog

Lake Oswego, OR · On-site

$207K/yr

We are a pioneer in developing innovative implantable medical device technologies and devices that save and enhance the quality of life for millions of individuals living with cardiovascular and ...

Showing results 41-60

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:

Manufacturing Specialist (Quality Assurance, Receiving, Inspection)

BIOTRONIK SE & Co.KG

Lake Oswego, OR • On-site

$60 - $80/hr

Other

Posted 6 days ago


Key responsibilities

  • Perform visual inspection on incoming components using automated inspection equipment and microscopes.

  • Set up inspection and handling equipment, including programming component test equipment, to meet specific inspection requirements.

  • Operate, perform routine maintenance, and troubleshoot automated equipment, tools, and systems related to inspection processes.


Job description

Career Opportunities: Manufacturing Specialist (Quality Assurance, Receiving, Inspection) (62504)

Requisition ID62504-Posted07/31/2026- Posting Country (1) - Work Location (1) -Manufacturing-Undefined-Full-time-Professionals-MST

Working for Micro Systems Engineering, Inc. (MSEI) means joining an elite team to work on some of the most exciting challenges in medical technology today. We are a pioneer in developing innovative implantable medical device technologies and devices that save and enhance the quality of life for millions of individuals living with cardiovascular and chronic neurologic pain disorders. With more than 40 years of experience in design and manufacturing active implantable medical devices, our continuing success is based on our company’s core values - innovation, quality, reliability, integrity, teamwork, and undisputed expertise - thus enabling usto inspire confidence and trust in physicians and patients worldwide. We are continually looking for talented engineers, scientists, and professionals to share in our mission.

Manufacturing Specialist (Quality Assurance, Receiving, Inspection)

Join our Manufacturing team as a QARI (Quality Assurance, Receiving, Inspection) Specialist. In this critical role, you’ll be responsible for ensuring the integrity of incoming components through precise electrical testing, detailed visual inspections, and adherence to established quality protocols. You’ll set up and operate inspection equipment, verify product specifications, and manage the complete testing cycle-from evaluation and documentation to final disposition or shipment.

PRIMARY RESPONSIBILITIES:

  • Perform visual inspection on incoming components using automated inspection equipment and a variety of microscopes.
  • Prioritization of incoming tasks and disposition of incoming material according to the requirements of the material management system (SAP).
  • Setup inspection and handling equipment to meet the requirements for specific incoming inspection tasks. This includes programming of component test equipment.
  • Setup, operate, and perform routine maintenance on automated equipment, tools, and systems.
  • Responsible for status monitoring and first-level troubleshooting, equipment recoveries and repairs that are commensurate with applicant’s level of expertise, training, and latitude provided by various Engineering groups.
  • Follow released work instructions and receive verbal or written instructions regarding duties to be performed, including special requests with limited documentation.
  • Performs quality charting, analyzing, interpreting data tracking, and running reports through our automated systems for continuous improvement and tracking of factory deliverables.
  • Escalate nonconforming processes, components, designs to product specification and any procedures that cannot be performed as documented.
  • Documentation of process changes when the need arises, due to any factors that may influence those processes.
  • Other duties may be assigned at the discretion of the manager.

EDUCATION / EXPERIENCE REQUIREMENTS:

  • Associate degree or high school diploma with equivalent work experience in related field
  • Experience in SMT assembly, component packaging, or wafer processing
  • Verbal and written communication skills
  • MS Office and general computer proficiency
  • Ability to use a microscope
  • Ability to work independently with minimal direction
  • Critical thinking skills
  • Detail oriented

ADDITIONAL PREFERRED KNOWLEDGE, SKILLS, ABILITIES:

  • Experience with SAP
  • Experience operating automated equipment
  • Experience in electronics manufacturing

PHYSICAL REQUIREMENTS:

The physical demands described within this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • While performing the duties of this job, the employee is regularly required to be independently mobile
  • The employee is also required to interact with a computer for extended periods of time and communicate with co-workers
  • The employee is required to use a microscope
  • Must be able to work a minimum of 40 hours / week

Working hours: Full-time

Job ID: 62504

Micro Systems Engineering, Inc. is an equal opportunity employer. In accordance with applicable law, the company prohibits discrimination based on race, color, religion, creed, gender, pregnancy or related medical conditions, age, national origin or ancestry, physical or mental disability, sexual orientation, genetic information, uniformed service or any other consideration protected by federal state and local laws. Our commitment to equal opportunity employment applies to all persons involved in our operations and prohibits unlawful discrimination by any employee.

#J-18808-Ljbffr