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Costa Rica Medical Device Quality Jobs in Indiana

INCOG

Senior QA Risk Management Engineer

Fishers, IN · On-site

Provide QA risk management oversight for medical device and combination product (autoinjector, prefilled syringe, and similar device) assembly operations, ensuring compliance with ISO 13485 and ISO ...

JobRx, Inc.

Director of Quality

Greenfield, IN · On-site

$170 - $210/hr

Ensure site adherence to GMP, ISO 13485, FDA, EMA, and other applicable regulations for medical device, drug packaging and combination products. * Direct Quality Assurance, Quality Engineering ...

Imh

Additionally, the specialist must align tasks with a medical quality management system and have experience with healthcare and medical device regulatory, privacy, and risk management requirements.

Viant

Quality Inspector

Fort Wayne, IN · On-site

Experience: * 2+ years inspection experience in medical device or regulated manufacturing. Skills ... highest quality, life enhancing medical devices. We do this through our depth and breadth of ...

SQA Services

Quality Auditor - Pharmaceutical

Carmel, IN · Remote

$1.3K/day

Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries * Coordinate, prepare, execute, and deliver ...

SQA Services

Quality Auditor - Pharmaceutical

Warren, IN · Remote

$1.3K/day

Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries * Coordinate, prepare, execute, and deliver ...

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All JobsCosta Rica Medical Device Quality JobsCosta Rica Medical Device Quality Jobs in Indiana

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 Indiana? For Costa Rica Medical Device Quality jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Costa Rica Medical Device Quality jobs in Indiana look for? The top searched job categories for Costa Rica Medical Device Quality jobs in Indiana are:
What cities in Indiana are hiring for Costa Rica Medical Device Quality jobs? Cities in Indiana with the most Costa Rica Medical Device Quality job openings:
Costa Rica Medical Device Quality jobs near you
Infographic showing various Costa Rica Medical Device Quality job openings in Indiana as of June 2026, with employment types broken down into 5% Full Time, 66% Part Time, 27% Temporary, and 2% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution.

Quality Control Inspector

ARCH Global Precision

Warsaw, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Quality Control Inspector (2nd Shift)
Precision Matters. Your Expertise Makes the Difference.
ARCH Medical Solutions - Warsaw, IN
Are you an experienced Quality Inspector who enjoys working with advanced measurement technology and tight-tolerance medical device components? If you take pride in accuracy, solving quality challenges, and ensuring products meet the highest standards, we want to hear from you.
At ARCH Medical Solutions, you'll play a critical role in inspecting precision-manufactured medical components that help improve people's lives. Join a team that values craftsmanship, accountability, and continuous improvement.
Why Join ARCH?
  • Medical, Dental, Vision & Prescription Benefits on Day 1
  • 401(k) with Company Match
  • Quarterly Bonus Opportunity
  • Paid Time Off
  • 9 Company-Paid Holidays
  • Company-Paid Life Insurance
  • Employee Assistance Program
  • 4-Day Work Week - 10-Hour Shifts (Enjoy a 3-Day Weekend!)

What You'll Do
As a Quality Control Inspector, you will perform receiving, first article, in-process, and final inspections to ensure products meet all customer and company specifications.
Key responsibilities include:
  • Inspect precision medical device components using advanced measurement equipment
  • Perform first article, in-process, and final inspections
  • Operate and program inspection equipment as required
  • Record and analyze measurement data
  • Review blueprints, specifications, and quality documentation
  • Assist with troubleshooting out-of-spec conditions
  • Support process control and continuous improvement efforts
  • Ensure inspection records and certifications are completed accurately
  • Verify product conformity prior to shipment

What We're Looking For
Required Qualifications
  • Minimum 5 years of quality inspection experience
  • Experience operating a Coordinate Measuring Machine (CMM)
  • Experience operating a Keyence measurement system
  • Experience operating a Starrett HDV Comparator
  • Strong understanding of Geometric Dimensioning & Tolerancing (GD&T)
  • Ability to read and interpret engineering drawings and blueprints
  • Strong attention to detail and commitment to quality
  • Excellent problem-solving and communication skills

Preferred Experience
  • Medical device manufacturing experience
  • Tight-tolerance inspection experience
  • Experience with statistical process control (SPC)
  • Familiarity with precision inspection tools, including micrometers, calipers, bore gauges, thread gauges, height stands, and surface plates

Physical Demands and Work Environment
While performing the duties of this job, continuous mental and visual attention is needed. The ability to stand for a shift, sit, talk, and hear is frequently required. Lifting to 40 pounds occasionally is required. Exposure to manufacturing areas where temperature may vary, and personal protective equipment is required.
ADDITIONAL NOTES
ARCH Global Holdings is an Equal Opportunity Employee and wholeheartedly supports diversity in the workplace as a basic premise for business success. All employees of ARCH Global Holdings are employed on an at-will basis.
This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employee(s) will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments.
A review of this position has excluded the marginal functions of the position that are incidental to the performance of fundamental job duties. All duties and responsibilities are essential job functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbent(s) will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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