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Medical Device Phd Jobs in Arizona (NOW HIRING)

Stryker

Senior Staff Medical Writer (Remote)

Phoenix, AZ · On-site +1

$143K - $238K/yr

Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards. Preferred * Master's degree, PhD, PharmD, MD, MPH, RN, BSN ...

onsemi

Sr. Customer Quality Manager

Scottsdale, AZ · On-site

$150 - $200/hr

The position will require a strong medical device as well as semiconductor quality background, as ... Qualifications * Bachelor's/Master's/PHD in Engineering, Semiconductor/Quality, Electrical ...

Dexcom Inc.

Sr Hardware Engineer

Arizona City, AZ · On-site

$150 - $200/hr

... quality medical device products to patients around the world. Our team focuses on packaging ... Or a PhD and 0‑2 years experience. Disclosures Please note: The information contained herein is ...

Intel

Semiconductor Device Modeling Engineer

Phoenix, AZ · On-site

$149K - $284K/yr

PhD in Electrical Engineering or a related discipline with a minimum of 1 year of industry or ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Roche

Senior Software Engineer, Cybersecurity

Tucson, AZ · On-site

$104K - $193K/yr

Are you ready to shape the future of medical device instrument control software? We are seeking a ... OR, PhD degree in a directly related discipline + 2 years of related experience required. * Prior ...

BEPC INC

Be Seen First

Regulatory Affairs Manager - PHCS - 30522

Tucson, AZ · On-site

$45 - $55/hr

PhD with 3-5 years , Master's degree with 5-7 years , or Bachelor's degree with 6-8 years of ... the medical device, biotechnology, or in-vitro diagnostics industry. * Demonstrated ability to ...

IQVIA

Clinical Trial Psych Rater

Gilbert, AZ · Remote

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... MD, DO, or PhD preferred. * Experience: * Minimum 3 years administering psychiatric assessments ...

IQVIA

Clinical Trial Psych Rater

Scottsdale, AZ · Remote

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... MD, DO, or PhD preferred. * Experience: * Minimum 3 years administering psychiatric assessments ...

IQVIA

Clinical Trial Psych Rater

Glendale, AZ · Remote

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... MD, DO, or PhD preferred. * Experience: * Minimum 3 years administering psychiatric assessments ...

IQVIA

Clinical Trial Psych Rater

Gilbert, AZ · Remote

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... MD, DO, or PhD preferred. * Experience: * Minimum 3 years administering psychiatric assessments ...

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All JobsMedical Device Phd JobsMedical Device Phd Jobs in Arizona

Medical Device Phd information

See Arizona salary details

$19

$46

$90

How much do medical device phd jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for medical device phd in Arizona is $46.44, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $55.58 per hour, depending on experience, location, and employer.

What is a Medical Device PhD?

A Medical Device PhD is an individual who has earned a Doctorate (PhD) with a focus on medical devices, typically through research in biomedical engineering, materials science, or a related field. These professionals are experts in designing, developing, and testing medical technologies used for diagnosis, treatment, or monitoring of health conditions. They may work in academic research, the medical device industry, regulatory agencies, or clinical settings, contributing to the innovation and safety of medical products. Their work often involves multidisciplinary collaboration and advanced knowledge of engineering, biology, and regulatory standards.

What are the key skills and qualifications needed to thrive as a Medical Device PhD, and why are they important?

To thrive as a Medical Device PhD, you need a doctoral degree in biomedical engineering or a related field, with expertise in medical device design, development, and regulatory standards. Familiarity with technical tools such as CAD software, statistical analysis programs, and knowledge of FDA or CE regulatory processes is crucial. Strong problem-solving, communication, and project management skills set top candidates apart in multidisciplinary teams. These skills enable the successful creation, testing, and approval of innovative medical devices that meet safety and efficacy standards.

What are some common challenges faced by PhDs working in the medical device industry, and how can they be addressed?

PhDs entering the medical device industry often encounter challenges such as adapting to the fast-paced product development cycle, working within regulatory frameworks, and translating academic research into practical solutions. Success in this role requires strong communication skills to collaborate with cross-functional teams like engineering, marketing, and regulatory affairs. Building familiarity with industry standards (e.g., ISO 13485, FDA regulations) and gaining hands-on experience with project management can help address these challenges and ensure a smooth transition from academia to industry.

What is the difference between Medical Device Phd vs Medical Device Engineer?

AspectMedical Device PhdMedical Device Engineer
Required CredentialsPhD in relevant field, research experienceBachelor's or Master's in engineering or related field
Work EnvironmentResearch labs, development teams, academiaDesign, testing, manufacturing settings
Employer & Industry UsageUniversities, research institutions, R&D departmentsMedical device companies, manufacturing firms
Common Search & ComparisonYesYes

The Medical Device Phd typically focuses on research, development, and innovation in medical devices, often working in labs or academia. In contrast, Medical Device Engineers are more involved in designing, testing, and manufacturing medical devices in industry settings. Both roles require technical knowledge, but their daily tasks and work environments differ significantly.

What can I do with a medical device PhD?

A medical device PhD prepares individuals for research, development, and regulatory roles in the medical device industry. Graduates can work in product design, clinical evaluation, quality assurance, or regulatory affairs, often utilizing skills in biomedical engineering, data analysis, and medical sciences. These roles are typically found in healthcare companies, research institutions, or regulatory agencies.

What are popular job titles related to Medical Device Phd jobs in Arizona?

For Medical Device Phd jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Medical Device Phd jobs in Arizona look for?

The top searched job categories for Medical Device Phd jobs in Arizona are:

What cities in Arizona are hiring for Medical Device Phd jobs?

Cities in Arizona with the most Medical Device Phd job openings:

Medical Device Phd jobs near you
Infographic showing various Medical Device Phd job openings in Arizona as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $96,601 per year, or $46.4 per hour.

Senior Staff Medical Writer (Remote)

Stryker

Phoenix, AZ • On-site, Remote

$143K - $238K/yr

Full-time

Posted 21 days ago

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

136th of 499 rated machine equipment manufacturers

Job description

Work Flexibility: Remote

Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. Our Endoscopy Division delivers a diverse array of innovative medical technologies to support minimal invasive surgery through brilliant visualization, connected OR solutions, sports medicine products to sustainability solutions.

As the Senior Staff Medical Writer, you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to translate complex clinical evidence into high-quality regulatory and scientific documents throughout the product lifecycle.

What You Will Do

  • Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management.

  • Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents.

  • Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access.

  • Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.

  • Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives.

  • Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation.

  • Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals.

  • Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members.

What You Need

Required

  • Bachelor's degree in a scientific, technical, healthcare, or related discipline.

  • Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products.

  • Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities.

  • Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation.

  • Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device Coordination Group (MDCG) guidance for clinical evaluations.

  • Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools.

  • Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards.

Preferred

  • Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

  • Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications.

  • Experience supporting regulatory submissions and global market access initiatives for medical devices.

  • Knowledge of clinical operations, risk management, and international regulatory requirements.

United States of America Pay Ranges:

  • USN: $110,100 - $183,400 USD Annual
  • US5: $115,600 - $192,600 USD Annual
  • US10: $121,100 - $201,700 USD Annual
  • US15: $126,600 - $210,900 USD Annual
  • US20: $132,100 - $220,100 USD Annual
  • US30: $143,100 - $238,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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