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Costa Rica Medical Device Quality Jobs in Wisconsin

Operator II

Hudson, WI

$19.50 - $20.50/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 ...

Medical Device Technician

Madison, WI · On-site

$38K - $48K/yr

Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions * Assemble, test, and repair work per established work instructions, policies ...

Operator II

Hudson, WI · On-site

$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 ...

Medical Device Technician

Madison, WI · On-site

$38K - $48K/yr

Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions * Assemble, test, and repair work per established work instructions, policies ...

WI · On-site

$98 - $153/hr

Knowledge The role requires extensive integrated knowledge of assigned products to support medical device quality, compliance, and safety throughout the product lifecycle, from product development ...

Knowledge of Medical Device Risk Management Regulation ISO 14971. * Ability to communicate ... Experience with content management/quality systems, archiving and control techniques.

Quality Engineer II

Kenosha, WI · On-site

$70K - $90K/yr

Knowledge of the medical device manufacturing industry is highly preferred. * Experience with CNC machining and mechanical inspection is preferred. * Knowledge of ISO 13485 Quality Management System ...

Quality Engineer II

Kenosha, WI · On-site

$70K - $90K/yr

Knowledge of the medical device manufacturing industry is highly preferred. * Experience with CNC machining and mechanical inspection is preferred. * Knowledge of ISO 13485 Quality Management System ...

WI · On-site

$91.62 - $152.70/hr

The role requires extensive integrated knowledge of assigned products to support medical device quality, compliance, and safety throughout the product lifecycle, from product development through ...

Be Seen First

Preparing samples for Quality analysis Equipment Set-Up and Operation: Operate equipment related to ... Experience working in a cleanroom environment with medical product manufacturing and/or with ...

Medical Device Assembler

Franksville, WI · On-site

$17.75 - $21.75/hr

... for Quality analysis Equipment Set-Up and Operation: Operate equipment related to media ... medical product manufacturing and/or with computers a plus. • Ability to sit and stand for ...

Quality Engineer

Menomonie, WI · On-site

$71K - $91K/yr

Develop and maintain quality plans for new medical device product introductions. * Ensure program compliance with regulatory requirements, including FDA (21 CFR 4, 11, 210, 211, 820), GMP, ISO 13485 ...

As a Medical Device Test Engineer, you will be part of the Quality Assurance department supporting the testing and validation of medical devices used in invasive cardiology. The ideal candidate will ...

Senior Medical Device Technician Job Category: University Staff Employment Type: Regular Job Profile: Instrument Technician Job Duties: Position facilitates day-to-day operation of a medical device ...

Showing results 21-40

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 Wisconsin?

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

What cities in Wisconsin are hiring for Costa Rica Medical Device Quality jobs?

Cities in Wisconsin with the most Costa Rica Medical Device Quality job openings:

$19.50 - $20.50/hr

Temporary

Re-posted 29 days ago


Resonetics rating

7.1

Company rating: 7.1 out of 10

Based on 28 frontline employees who took The Breakroom Quiz


Job description

Overview

This position employs an individual for the advanced operation of a computer-based laser machining work center. This individual's primary responsibility will be to laser process components through minimum instructions that may be in the form of drawings and written or verbal direction, and complete visual inspections. Employee must become familiar with concepts of procedures and are aided with general supervision. Additionally, the individual in this position may be asked to provide leadership and direction to newly hired or more junior employees. This position is part of a team and a heavy emphasis will be placed on the individual's ability to participate in a team environment.

Shift: Weekend Days - Friday: 10am-10pm, Saturday & Sunday: 8am-8pm

Responsibilities
  • Perform medium to high complexity tasks related to customer specific process requirements. Must be able to comprehend documentation requirements.
  • Verify system conditions or equipment status before operation. Employee may be required to adjust system settings within established guidelines
  • Inspect components to insure specifications have been met. Must be able to complete visual inspections on product. 
  • Enter data and report issues as required.
  • Take responsibility as directed for all required process documentation
  • Train other employees on production processes or equipment usage as requested by Supervisor.
  • Maintain a clean and safe work area.
  • Follows instructions of the Supervisor and/or Production Manager and conduct all work according to Resonetics policy and good safe labor practices.
  • The use of laser radiation (non-ionizing) sources will be used only in a manner that is safe for all Resonetics employees and visitors. The various wavelengths of laser light utilized at Resonetics will be taken into consideration in this and other personal protection policies by the laser operator.
  • Employee must conduct themselves in a professional and appropriate manner and is responsible for maintaining a high standard of conduct and job performance.
Required Qualifications
  • High School Diploma or Equivalent or completion of primary school in Costa Rica
  • Minimum three years of experience in a comparable manufacturing environment preferably utilizing computer aided machinery or similarly equivalent experience demonstrating the ability to follow detailed technical processes using mechanical equipment.
Preferred Qualifications
  • Experience with automated inspection equipment
  • Familiarity with ISO Quality Systems particularly in medical device manufacturing. 
  • Use of optical inspection equipment. This may be defined as a magnifier, microscope, and/or equipment used for measuring capacity.
Physical Demands
  • Good dexterity as many jobs require the handling of many small components.
Compensation

The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $19.50-20.50/hr

For temp, temp-to-hire, and regular full-time positions, our company policy is that we are unable to provide visa sponsorship. Candidates must already be legally authorized to work in the United States without the need for sponsorship now or in the future.

Employment Type: TEMPORARY

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