ZipRecruiter

Log In

1

Fda Cdrh Jobs (NOW HIRING)

Quest Global

Safety Engineer

Dallas, TX

$45 - $55/hr

Creates/updates IEC 60825-1 and CDRH laser reports according to Form FDA 3632. * Perform regulatory impact assessments for new product standards and/or changes to existing standards affecting company ...

Hologic

Quality Engineer 3

San Diego, CA · On-site

$76K - $98K/yr

Working knowledge of applicable FDA and ISO regulations and expectations, including CDRH, CBER, 21 CFR Part 820, 21 CFR Part 11, ISO 13485 and ISO 14971. * Cleanroom manufacturing experience ...

next page

Showing results 1-20

All JobsFda Cdrh Jobs

Fda Cdrh information

See salary details

$13

$39

$76

How much do fda cdrh jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for fda cdrh in the United States is $39.35, according to ZipRecruiter salary data. Most workers in this role earn between $24.52 and $49.04 per hour, depending on experience, location, and employer.

Is the CDRH part of the FDA?

Yes, the Center for Devices and Radiological Health (CDRH) is a part of the U.S. Food and Drug Administration (FDA). It is responsible for regulating medical devices, radiation-emitting products, and ensuring their safety and effectiveness. Professionals working as FDA CDRH staff typically need knowledge of regulatory requirements, medical device standards, and may require relevant certifications.

What is the highest paying job at the FDA?

The highest paying job at the FDA is typically a senior leadership role such as the Director of the Center for Devices and Radiological Health (CDRH) or other executive positions, which can have salaries exceeding $200,000 annually. These roles often require advanced degrees, extensive experience, and leadership skills, and may include additional benefits and bonuses.

Is FDA on a hiring freeze?

The FDA's Center for Devices and Radiological Health (CDRH) is subject to federal hiring policies, which can include hiring freezes during budget constraints or government shutdowns. Currently, there is no publicly announced nationwide hiring freeze specific to FDA CDRH positions, but hiring practices may vary based on agency priorities and funding. Job seekers should monitor official FDA announcements and USAJOBS for current opportunities and updates.

What is the difference between Fda Cdrh vs Fda Cdrh?

AspectFda Cdrh

Since the comparison is between the same job title, Fda Cdrh vs Fda Cdrh, there is no difference. Both roles involve regulatory oversight of medical devices, require similar certifications, and are employed within the FDA's Center for Devices and Radiological Health. The responsibilities, work environment, and industry usage are identical, making them essentially the same position.

Is it hard to get hired by the FDA?

Getting hired as an FDA CDRH professional can be competitive due to the specialized nature of the role and the agency's rigorous hiring process. Candidates typically need relevant education, experience in medical device regulation, and often must pass background checks and assessments. Strong knowledge of FDA regulations and certifications can improve chances of employment.

What types of cross-functional collaboration can I expect in an FDA CDRH role?

In an FDA Center for Devices and Radiological Health (CDRH) position, you'll frequently work with multidisciplinary teams, including scientists, engineers, medical officers, and regulatory specialists. Collaboration is essential for reviewing medical device submissions, conducting safety evaluations, and developing regulatory policies. You'll often participate in meetings, share findings, and contribute your expertise to ensure that devices meet federal safety and efficacy standards. This collaborative approach not only enriches your own knowledge but also ensures comprehensive oversight of medical devices.

What are the key skills and qualifications needed to thrive as an FDA CDRH (Center for Devices and Radiological Health) professional, and why are they important?

To thrive as an FDA CDRH professional, you need a background in biomedical engineering, life sciences, or a related field, often with advanced degrees and experience in regulatory affairs. Familiarity with regulatory submission systems (like eSTAR, eCopy), FDA guidance documents, and certifications such as RAC (Regulatory Affairs Certification) are typically important. Strong analytical skills, attention to detail, and clear communication are essential for evaluating medical device safety and efficacy and collaborating across teams. These competencies ensure compliance, protect public health, and support the timely approval of safe and effective medical devices.

What is the FDA CDRH?

The FDA CDRH stands for the Center for Devices and Radiological Health, which is a branch of the U.S. Food and Drug Administration. Its primary role is to ensure the safety and effectiveness of medical devices and radiation-emitting electronic products in the United States. The CDRH oversees the premarket approval process, monitors postmarket performance, and enforces regulations to protect public health. It also provides guidance to manufacturers, healthcare professionals, and consumers regarding medical devices and their safe use.
More about Fda Cdrh jobs
What cities are hiring for Fda Cdrh jobs? Cities with the most Fda Cdrh job openings:
What states have the most Fda Cdrh jobs? States with the most job openings for Fda Cdrh jobs include:
What job categories do people searching Fda Cdrh jobs look for? The top searched job categories for Fda Cdrh jobs are:
Fda Cdrh jobs near you
Infographic showing various Fda Cdrh job openings in the United States as of July 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 72% In-person, 14% Hybrid, and 14% Remote job distribution, with an average salary of $81,843 per year, or $39.3 per hour.
Safety Engineer

Safety Engineer

Quest Global

Dallas, TX

$45 - $55/hr

Full-time

Posted 6 days ago

Quest Global rating

7.4

Company rating: 7.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

244th of 369 rated engineering

Job description

Job Requirements

Job Description

Who We Are:

Quest Global delivers world-class end-to-end engineering solutions by leveraging our deep industry knowledge and digital expertise. By bringing together technologies and industries, alongside the contributions of diverse individuals and their areas of expertise, we are able to solve problems better, faster. This multi-dimensional approach enables us to solve the most critical and large-scale challenges across the aerospace & defense, automotive, energy, hi-tech, healthcare, medical devices, rail and semiconductor industries.

We are looking for humble geniuses, who believe that engineering has the potential to make the impossible possible; innovators, who are not only inspired by technology and innovation, but also perpetually driven to design, develop, and test as a trusted partner for Fortune 500 customers. As a team of remarkably diverse engineers, we recognize that what we are really engineering is a brighter future for us all. If you want to contribute to meaningful work and be part of an organization that truly believes when you win, we all win, and when you fail, we all learn, then we’re eager to hear from you. The achievers and courageous challenge-crushers we seek, have the following characteristics and skills.


What You will Do:

Safety Engineer - Medical products – 6+ Years Experience

Primary Job function - 

  •     Experience with Safety concepts, standards and test methods and how they relate to products. Facilitates a systems-level approach to Product Safety compliance for new product development and design changes to existing product.
  •    Working knowledge of test set up and execution as required per UL/CSA/IEC 61010-1 and 61010-2-101 and other 61010 particulars as applicable. Provides guidance to test technicians and junior engineers on Product Safety test setup, execution and troubleshooting.
  •     Actively participates in UL witness testing with UL engineers for changes to existing product and new product launches.
  •     Conduct quarterly UL audits for company manufactured product and ISO 17025, addresses any variation notices.
  • Performs basic EMC/Safety assessments for design changes to existing product, providing design recommendations to R&D engineers and management. Regularly communicates directly with UL/EU Notified Body on design changes
  •   Creates/updates IEC 60825-1 and CDRH laser reports according to Form FDA 3632.
  •   Perform regulatory impact assessments for new product standards and/or changes to existing standards affecting company products.

What You will bring:

  •     Hands-on technical knowledge and expertise of Product Safety test methods and test equipment, procedures, and standards.
  •      Completes professional level engineering assignments related to Product Safety. Leads and participates in projects involving the design, fabrication, and manufacture of complex instrument subassemblies, systems or processes.
  •     Collaborates across functional areas, including engineering, project management and other systems development personnel.
  •     Maintains test capability by researching required test equipment to align with regulatory changes and/or product changes/enhancements.
  •     Creates and/or maintains internal test procedures according to associated external test method standards, directives and regulations.
  •   Responsible for implementing and maintaining the effectiveness of the quality system.
  •    Maintains lab areas in a state of audit readiness, following cGMP practices. Assists with metrology requirements for equipment calibration and OOT assessments.
  •      Consistently meets timelines for the completion of Product Safety related activity in support of program timelines.
  •     Strong organizational skill, follow-up and attention to detail. Strong written and verbal communication skills.
  •     Travel as necessary to aid in program facilitation or for training (5%)

Qualifications/Experience/Education Requirements       

Basic Qualifications:

Bachelor's degree in an engineering or closely related discipline with 6+ years progressive work experience in laboratory environment, field service, Safety and/or with Abbott Diagnostics products. 


Preferred Qualifications:

Bachelor’s Degree in Electrical, Mechanical, or Biomedical Engineering with a minimum of 6+ years work experience in Medical Device Product Safety testing.

Pay Range:$45-$55/hr on C2C

Work Requirements:

This role is considered an on-site position located in Irving, TX

  • You must be able to commute to and from the location with your own transportation arrangements to meet the required working hours.

What Quest Global employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply