Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...
Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...
Medical Coder Specialist
Indianapolis, IN · On-site
Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...
Medical Coder Specialist
Indianapolis, IN · On-site
Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...
Medical Coder Specialist
Indianapolis, IN · On-site
Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...
Medical Coder Specialist
Indianapolis, IN · On-site
Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...
Medical Coder Specialist
Carmel, IN · On-site
Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...
Medical Coder Specialist
Carmel, IN · On-site
Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...
Quality Engineer
Warsaw, IN · On-site
$60K - $78K/yr
Medical device, particularly Orthopedic industry, experience preferred
Quality Engineer
Warsaw, IN · On-site
$60K - $78K/yr
Medical device, particularly Orthopedic industry, experience preferred
Quality Engineer
Noblesville, IN · On-site
$67K - $87K/yr
Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...
Quality Engineer
Noblesville, IN · On-site
$67K - $87K/yr
Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...
Director, Quality Microbiology
$166K - $228K/yr
SUMMARY The Director, Quality Microbiology, is responsible for leading Integra LifeSciences ... Minimum 12 years' experience in medical device or regulated industry with 5 years of leadership ...
Director, Quality Microbiology
$166K - $228K/yr
SUMMARY The Director, Quality Microbiology, is responsible for leading Integra LifeSciences ... Minimum 12 years' experience in medical device or regulated industry with 5 years of leadership ...
Design Quality Engineer
Indianapolis, IN · On-site
Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO ...
Design Quality Engineer
Indianapolis, IN · On-site
Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO ...
Quality & Regulatory Specialist - FDA QMSR & ISO 13485 Medical Device Manufacturing Company Overview Med-Mizer is a leading manufacturer of hospital beds, specialty seating, and safe patient-handling ...
Quality & Regulatory Specialist - FDA QMSR & ISO 13485 Medical Device Manufacturing Company Overview Med-Mizer is a leading manufacturer of hospital beds, specialty seating, and safe patient-handling ...
Design Quality Engineer
Indianapolis, IN · On-site
Location: ~Indianapolis, IN~ (REMOTE) Duration: 6 months Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control ...
Design Quality Engineer
Indianapolis, IN · On-site
Location: ~Indianapolis, IN~ (REMOTE) Duration: 6 months Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control ...
Quality & Regulatory Specialist - FDA QMSR & ISO 13485 Medical Device Manufacturing Company Overview Med-Mizer is a leading manufacturer of hospital beds, specialty seating, and safe patient-handling ...
Quality & Regulatory Specialist - FDA QMSR & ISO 13485 Medical Device Manufacturing Company Overview Med-Mizer is a leading manufacturer of hospital beds, specialty seating, and safe patient-handling ...
Manufacturing Engineer II - Exempt
Warsaw, IN · On-site
$50 - $52/hr
Experience with change control in Medical Device Quality System Education Required: * Bachelors Degree in Engineering discipline and at least 2 years of relevant experience providing direct ...
Quick apply
Manufacturing Engineer II - Exempt
Warsaw, IN · On-site
$50 - $52/hr
Experience with change control in Medical Device Quality System Education Required: * Bachelors Degree in Engineering discipline and at least 2 years of relevant experience providing direct ...
Director of Quality
Greenfield, IN · On-site
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 ...
Director of Quality
Greenfield, IN · On-site
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 ...
Quality Assurance Engineer
Indianapolis, IN · On-site
$95K - $103K/yr
Ensure compliance with FDA, ISO 13485, and other applicable regulatory requirements for medical device manufacturing. Develop, implement, and maintain Quality Management System (QMS) documentation ...
Quality Assurance Engineer
Indianapolis, IN · On-site
$95K - $103K/yr
Ensure compliance with FDA, ISO 13485, and other applicable regulatory requirements for medical device manufacturing. Develop, implement, and maintain Quality Management System (QMS) documentation ...
Director of Quality
Greenfield, IN · On-site
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 ...
Director of Quality
Greenfield, IN · On-site
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 ...
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 ...
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 ...
Design Quality Engineer
Warsaw, IN · On-site
Role: Design Quality Engineer Location: Warsaw, IN & Raynham, MA (Onsite) Duration: 6-Month ... medical device environment. This role will be responsible for ensuring compliance with design ...
Quick apply
Design Quality Engineer
Warsaw, IN · On-site
Role: Design Quality Engineer Location: Warsaw, IN & Raynham, MA (Onsite) Duration: 6-Month ... medical device environment. This role will be responsible for ensuring compliance with design ...
Quality Line Reference (Inspection)
Fishers, IN · On-site
$29/hr
Vision insurance Schedule: * 8 hour shift Experience: * performing quality control test: 3 years (Required) * healthcare environment (medical device or phrama): 3 years (Required) * visually ...
Quick apply
Quality Line Reference (Inspection)
Fishers, IN · On-site
$29/hr
Vision insurance Schedule: * 8 hour shift Experience: * performing quality control test: 3 years (Required) * healthcare environment (medical device or phrama): 3 years (Required) * visually ...
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 ...
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 ...
Ensure compliance with FDA, ISO 13485, and other relevant regulatory standards for medical device manufacturing. * Develop and implement quality management system documents for product design ...
Ensure compliance with FDA, ISO 13485, and other relevant regulatory standards for medical device manufacturing. * Develop and implement quality management system documents for product design ...
Costa Rica Medical Device Quality information
What is a Costa Rica medical device quality job?
What are the key skills and qualifications needed to thrive in medical device quality roles in Costa Rica?
What are common challenges faced by professionals working in medical device quality roles in Costa Rica, and how can they be addressed?
What is the difference between Costa Rica Medical Device Quality vs Costa Rica Medical Device Regulatory Affairs Specialist?
| Aspect | Costa Rica Medical Device Quality | Costa Rica Medical Device Regulatory Affairs Specialist |
|---|---|---|
| Certifications | ISO 13485, internal quality audits | Regulatory compliance, local and international approvals |
| Work Environment | Manufacturing sites, quality control labs | Regulatory agencies, documentation review |
| Industry Usage | Quality assurance, process improvement | Regulatory 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 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:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 17 days ago
Job description
In Some Jobs You Take Orders. In This One, You Write History.
Join the healthcare information technology team that's turning drug and medical device data into knowledge used by thousands of hospitals; the majority of U.S. health plans, retail pharmacies, and pharmacy benefit managers; and millions of healthcare decision makers throughout the world. Partnering with our information system developer and healthcare institution customers, you'll help evolve leading-edge thinking into reality and make a measurable difference in improving human health.
We're looking for people who are: Intelligent. Productive. Committed. Willing and able to go above and beyond. Passionate about making a difference. Innovative. Energized. And want to play an essential role in a successful company's continued growth.
Are you ready for this exciting challenge?
____________________________________________________________________________________________
First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from the FDA, device manufactures, and other credible sources to generate unbiased, robust medical device content for our device solution with an emphasis on HCPCS coding for medical devices.
This position is based out of our Carmel office and follows a hybrid work model, with an expectation to work onsite at least three days per week.
Responsibilities:
- Researches pertinent information from various sources such as manufacturers and CMS to assign the Healthcare Common Procedure Coding System (HCPCS) codes, to medical device content.
- Update and maintain our HCPCS library through detailed research.
- Uses research to develop and maintain HCPCS mapping and wizard.
- Provides training to staff members.
- Ensure accuracy of codes applied to devices using data audits, validations and reviews.
- Updates HCPCS codes as changes are made to GMDN and/or UNSPSC categories.
- Evaluates current categorization schema and provides feedback and training to categorization staff.
- Evaluates medical device content to ensure the accuracy of HCPCS mappings.
- Follows up with manufacturers when code assignments are not straightforward or data is inadequate, ambiguous, or unclear for coding purposes.
- Ensures updates from CMS are applied to data in a timely manner using maintenance tools.
- Ensures accuracy of codes and codes are current and active.
- Searches for information in cases where the coding is complex or unusual.
- Abides by the Standards of Ethical Coding as set forth by the American Health Information Management Association and adheres to official coding guidelines.
- Keeps abreast of and complies with coding guidelines and reimbursement reporting requirements
Required Skills:.
- Ability to research devices, categories, and HCPCS codes leading to the development of a library.
- Expertise in oral and written communications -ability to clarify and discuss coding issues with peers.
- Able to multi-task and prioritize tasks.
- Good written and verbal communication skills.
- Attention for detail and strong organizational skills.
- Medical terminology and coding.
- Ability to use web based and computer applications and work with peers in team situations.
- Takes initiative in performing additional tasks.
- Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
- Skilled in developing structured prompts and reusable AI-assisted workflows to compare source data, identify inconsistencies, summarize research findings, and support coding-related decision making.
- Demonstrates responsible use of AI by validating all AI-generated outputs against credible sources, official coding guidance, internal standards, and professional judgment.
- Maintains compliance with data privacy, company security policies, ethical coding standards, and appropriate human oversight when using AI tools.
Relevant Experience:
- Minimum of 2-3 years of medical coding experience in a healthcare setting, including outpatient clinics, ambulatory surgical centers (ASCs), home health, or Durable Medical Equipment (DME) settings.
- Experience assigning or auditing HCPCS Level II code sections, including A-codes, C-codes, or E-codes.
- Experience reviewing or resolving Medicare and Medicaid claim denials involving medical necessity, unlisted HCPCS codes, or Medically Unlikely Edits (MUEs).
- Experience researching and applying Medicare Local Coverage Determinations (LCDs) and National Coverage Determinations (NCDs).
- Previous experience in supply chain management or medical device industry preferred.
- Active coding certification from AAPC or AHIMA. Relevant credentials include: Certified Professional Coder (CPC) certification, Certified Outpatient Coder (COC), or Certified Coding Specialist (CCS).
_____________________________________________________________________________________________
About FDB:
FDB is the leading provider of drug and medical device knowledge that helps healthcare professionals make precise decisions. With thousands of customers worldwide, FDB enables our information system developer partners to deliver valuable, useful, and differentiated solutions. We offer more than three decades of experience in transforming medical knowledge into actionable, targeted, and effective solutions that help improve patient safety, operational efficiency, and healthcare outcomes. For a complete look at our solutions and services, please visit www.fdbhealth.com or follow us on and LinkedIn.
We value Integrity, Respect, Responsibility, Teamwork, and Creativity. Our offices in South San Francisco and Indianapolis have been awarded with Top Workplaces honors by The Bay Area News Group and the Indy Star, since 2016 (the Top Workplaces honors are based solely on the results of an employee feedback survey by a leading research firm that specializes in organizational health and workplace improvement). FDB offers competitive salaries and extensive benefits - including medical, dental, vision, long term disability, life insurance, and matching 401k.
We are an Equal opportunity employer - vets/disabled. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state, or local law.
First Databank, Inc. (FDB) endeavors to make www.fdbhealth.com accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email accommodations@fdbhealth.com. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.
For more information about our commitment to equal employment opportunity, please visit EEO is the Law, EEO is the Law Supplement, Pay Transparency, and FDB EEO/AA Statement.
In accordance with applicable law, Hearst is required to include a reasonable estimate of the compensation for this role if hired in Carmel, IN. The reasonable estimate is $47,000 to $57,000. Please note this information is specific to those hired in location. If this role is open to candidates outside of location, the salary range would be aligned to that specific location. A final decision on the successful candidate's starting salary will be based on a number of permissible, non-discriminatory factors, including but not limited to skills and experience, training, certifications, and education.
This role is also eligible for a competitive benets package that includes medical, dental, vision, life, and disability insurance; 401(k) retirement plan; exible spending savings account; paid holidays; paid time off; employee assistance program; and other company benets.
About First DataBank
Sourced by ZipRecruiter
Company size
201 - 500 Employees
Headquarters location
South San Francisco, CA, US
Year founded
1977