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Fda Jobs in Arizona (NOW HIRING)

CCRM Fertility

Physician Assistant

Scottsdale, AZ · On-site

$101K - $137K/yr

Initiate new egg donor and gestational carrier consultations; complete full work up IAW FDA regulations. * Develop and implement patient management plans and collaborate with the physician team to ...

ECN Operating LLC

Physician - Dermatologist

Chandler, AZ · On-site

$200 - $250/hr

Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP , FDA, and sponsor requirements. * Participate in Site Initiation Visits (SIVs) , Monitoring Visits , and Audits ...

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$13

$38

$74

How much do fda jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for fda in Arizona is $38.20, according to ZipRecruiter salary data. Most workers in this role earn between $23.80 and $47.61 per hour, depending on experience, location, and employer.

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.

What are the most commonly searched types of Fda jobs in Arizona?

The most popular types of Fda jobs in Arizona are:

What are popular job titles related to Fda jobs in Arizona?

For Fda jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Fda jobs in Arizona look for?

The top searched job categories for Fda jobs in Arizona are:

What cities in Arizona are hiring for Fda jobs?

Cities in Arizona with the most Fda job openings:

Fda jobs near you
Infographic showing various Fda job openings in Arizona as of August 2026, with employment types broken down into 77% Full Time, 11% Part Time, and 12% Contract. Highlights an 100% In-person job distribution, with an average salary of $79,460 per year, or $38.2 per hour.

Sr. R&D Engineer- Relocation Assistance Provided

Innovative Health LLC

Scottsdale, AZ • On-site

$101K - $139K/yr

Full-time

This job post has expired 3 days ago. Applications are no longer accepted.

Job description

The Senior R&D Engineer role is responsible for designing, developing, validating, and implementing various methods and processes, leading and assisting in projects to introduce new products into production. This role is expected to bring unique perspectives and creative solutions to challenges faced during reverse engineering and reprocessing technique development.Essential Duties and Responsibilities:• Assist and/or lead in development of new medical device platforms complying with design control process including applicable FDA and ISO requirements.• Develop, write, and execute test methods.• Train manufacturing/QC personnel as needed on test methods or manufacturing processes.• Generate formal test protocols and reports.• Execute test protocols and conduct bench testing. Document test results per GDP, ISO, and FDA requirements.• Coordinate and oversee test sample builds. Assist with test sample builds as required.• Use Solidworks to design test fixtures and devices. (if applicable)• Design and fabricate test fixtures, tooling and equipment. (if applicable)• Work with purchasing department to specify and procure capital equipment.• Serve as a cross-functional team member for various project-related activities.• Assist or lead process improvement projects to reduce costs.• Assist with DFMEA and PFMEA risk assessments.• Compile project status updates and present to senior management.• Comply with company policies and procedures.• Maintain project schedule and deliver projects on time.• Focus on delivering products to support the R&D project pipeline.• Provide technical leadership to junior engineers and technicians. Clinical Support Responsibilities:• Attend clinical cases for learning, device launch, and troubleshooting.• Interact with clinicians and field personnel to understand clinical needs and provide technical support.• Develop and maintain a deep understanding of medical device reprocessing techniques, including cleaning, sterilization, and biocompatibility requirements.• Develop and maintain relationships with key opinion leaders and clinical partners. Medical Device Reprocessing Responsibilities:• Develop and optimize reprocessing methods for single-use medical devices.• Conduct performance, biocompatibility and sterilization testing on reprocessed devices.• Ensure compliance with all regulatory requirements for medical device reprocessing.• Participate in cross-functional teams to introduce reprocessed devices into production.Supervisory Responsibilities:· Provide mentoring and guidance to other R&D team members, as well as supervise and manage the work of junior engineers.Education, Qualifications and Skills:· Minimum education: Bachelor's degree in engineering discipline (or equivalent experience)· Minimum experience: 7-12 years of experience· Strong background in R&D with experience in electromechanical medical devices.· Experience with various types of medical device design verification testing in accordance with FDA regulations: device functional performance, biocompatibility, sterilization, packaging, transportation simulation, real-time and accelerated aging, etc.· Excellent technical writing skills and substantial experience writing test plans, protocols, and reports.· Excellent problem-solving skills as well as keen analytical abilities.· Knowledge of Design Controls, Risk Management, Statistics, Engineering Principles, Test Method Development, Test Method Validation (Gage R&R), and Design Verification / Validation.· Proficiency in CAD design and drafting (SolidWorks) a plus.· Ability to work in a fast-paced, collaborative team environment.· Strong hands-on prototyping skills.· Self-starter and highly motivated.· Ability to have fun by motivating and encouraging other team members.