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Medical Device Labeling Jobs in Arizona (NOW HIRING)

Machine/Saw Operator

Phoenix, AZ · On-site

$16.25 - $19.25/hr

Medical Device, and Mining. Our inventory is massive, quality standards unmatched, and our turn ... Maintains inventory by identifying, labeling, and keeping materials and supplies in stock ...

Machine/Saw Operator

Phoenix, AZ · On-site

$16.25 - $19.25/hr

Medical Device, and Mining. Our inventory is massive, quality standards unmatched, and our turn ... Maintains inventory by identifying, labeling, and keeping materials and supplies in stock ...

Production Lead Molding

Tempe, AZ · On-site

$18.25 - $25/hr

... label generation. * Maintains a clean, orderly and safe workstation and environment at all times ... Experience with cGMP practices, ISO, and medical device manufacturing * Experience supervising ...

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Showing results 1-20

Medical Device Labeling information

See Arizona salary details

$12

$28

$88

How much do medical device labeling jobs pay per hour?

As of Jun 30, 2026, the average hourly pay for medical device labeling in Arizona is $28.45, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $36.49 per hour, depending on experience, location, and employer.

What is a Medical Device Labeling job?

A Medical Device Labeling job involves creating, reviewing, and managing labeling content for medical devices to ensure compliance with regulatory requirements. This includes instructions for use, packaging labels, and safety information for healthcare professionals and patients. Professionals in this role collaborate with regulatory, quality, and engineering teams to meet industry standards and country-specific regulations. Their work ensures that medical devices are used safely and effectively, reducing risks associated with improper usage.

What are the key skills and qualifications needed to thrive in the Medical Device Labeling position, and why are they important?

To thrive in Medical Device Labeling, you need a strong understanding of regulatory requirements (such as FDA and EU MDR), attention to detail, and experience with technical writing or documentation, often supported by a degree in life sciences or a related field. Familiarity with labeling management systems, document control tools, and knowledge of ISO standards are key technical qualifications, and certifications like RAC can be advantageous. Strong communication, collaboration, and organizational skills set candidates apart, as these roles often involve coordinating with cross-functional teams such as regulatory, engineering, and quality assurance. These capabilities ensure labeling materials meet strict compliance standards, avoid costly errors or recalls, and support timely product launch and patient safety.

What are the typical daily responsibilities for someone working in Medical Device Labeling?

Professionals in Medical Device Labeling are responsible for creating, reviewing, and updating product labels, instructions for use, and packaging materials to ensure compliance with regulatory standards. They often collaborate closely with regulatory affairs, engineering, and quality assurance teams to gather technical product information and incorporate feedback. Daily activities may also include managing document control processes, implementing labeling changes driven by new regulations or product updates, and preparing submissions for global markets. Attention to detail and the ability to manage multiple projects simultaneously are crucial for success in this role.

What are the most commonly searched types of Medical Device Labeling jobs in Arizona? The most popular types of Medical Device Labeling jobs in Arizona are:
Infographic showing various Medical Device Labeling job openings in Arizona as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $59,169 per year, or $28.4 per hour.
Manager, Clinical Science, Medical Affairs

Manager, Clinical Science, Medical Affairs

Danaher

Phoenix, AZ • On-site, Remote

$150K - $170K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago


Key responsibilities

  • Develop and execute medical strategy aligned with product lifecycle stages, diagnostic priorities, and business objectives, ensuring scientific integrity and compliance.

  • Serve as a scientific expert and liaison to healthcare professionals, key opinion leaders, and internal stakeholders to facilitate clinical education, evidence exchange, and trusted relationships.

  • Lead generation, interpretation, and communication of medical evidence, including clinical data, real-world evidence, and publications, to support appropriate product use and informed decision-making.


Danaher rating

7.5

Company rating: 7.5 out of 10

Based on 28 frontline employees who took The Breakroom Quiz


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

Our team at Integrated DNA Technologies (IDT), is united by a commitment to collaboration and scientific excellence, building on a strong foundation of innovation, expertise, and reliability. Guided by our vision to help researchers rapidly move from the lab to life-changing advances, we work closely with global partners to accelerate progress and genomics breakthroughs across fields like cancer, infectious disease, rare genetic disorders, and more. At IDT, you'll be part of a culture rooted in continuous learning and improvement-where your growth fuels our mission to accelerate the pace of genomics and helps shape a healthier, brighter future for all.

Learn about the Danaher Business System which makes everything possible.

The Manager, Clinical Science, Medical Affairs is a critical strategic role in driving sustainable business value ensuring the scientific credibility, regulatory compliance and clinical relevance of the organization's products. This role will serve as a trusted scientific partner to internal/external stakeholders-including healthcare professionals, crossfunctional teams, and external collaborators - directly influencing product adoption, appropriate use, and longterm market success.

This position reports to the Director, Global Regulatory Affairs, Product Lifecycle Quality and Compliance and is part of the global QA/RA function located in Coralville, IA and will be fully remote.

In this role, you will have the opportunity to:

  • Develop and execute medical strategy aligned with product lifecycle stages, diagnostic priorities, and overall business objectives, ensuring scientific integrity and compliance.
  • Serve as a scientific expert and liaison to healthcare professionals, key opinion leaders, and internal stakeholders to facilitate clinical education, evidence exchange, and trusted relationships associated with off-label inquiries, third-party validation services, health hazard assessments, etc.
  • Lead generation, interpretation, and communication of medical evidence, including clinical data, realworld evidence, and publications, to support appropriate product use and informed decisionmaking.
  • Ensure regulatory, ethical, and compliance adherence across all medical activities, mitigating risk and maintaining a clear separation between medical and promotional functions.
  • Provide strategic medical insights to crossfunctional teams (commercial, market access, R&D, regulatory) to inform product development, launch planning, and postmarketing strategies.

The essential requirements of the job include:

  • Bachelor's degree in Biostatistics, Life Science, Chemistry, Biochemistry or equivalent; MD or PhD preferred
  • 5-10 years experience in Medical Device/Pharma/IVD companies
  • Experience in next generation sequencing with proficient knowledge of medical terminology
  • With minimal supervision, demonstrate a high level of customer service skills, approachability, and sense of urgency with strong collaboration skills (communication, tone, messaging, execution, planning, ownership).

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel 10% domestically, and internationally

It would be a plus if you also possess previous experience in:

  • a Medical Affairs role, such as a Medical Science Liaison (MSL)
  • Novel Biomarker Assay Development

IDT, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At IDT we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for IDT can provide.

The annual salary range for this role is $150,000 - $170,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.


For more information, visit www.danaher.com.


Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.


The U.S. EEO posters are available here.


For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.


We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984