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Medical Device Operations Jobs in Phoenix, AZ (NOW HIRING)

Provident Research Inc

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Senior Clinical Research Associate Cardiac Medical Device

Phoenix, AZ · Remote

$135K - $141K/yr

SR CRA Cardiac Medical Device (home based) Remote Become Part of a Major Initiative to Monitor Life ... Operations and Study Site personnel for the specific clinical projects. This opening is immediate ...

Stryker

Senior Staff Medical Writer (Remote)

Phoenix, AZ · On-site +1

$143K - $238K/yr

Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745 ... Knowledge of clinical operations, risk management, and international regulatory requirements.

AbbVie

Associate Director, Engineering

Tempe, AZ · On-site

... Medical Device Manufacturing performance. The position is on the Site Leadership Team and advises the Manufacturing Site Director and extended Operations leadership team on strategy and business ...

AbbVie

Associate Director, Engineering

Tempe, AZ · On-site

... Medical Device Manufacturing performance. The position is on the Site Leadership Team and advises the Manufacturing Site Director and extended Operations leadership team on strategy and business ...

AbbVie

Associate Director, Engineering

Tempe, AZ · On-site

$141K/yr

... Medical Device Manufacturing performance. The position is on the Site Leadership Team and advises the Manufacturing Site Director and extended Operations leadership team on strategy and business ...

Stryker Group

Senior Operations Manager

Phoenix, AZ · On-site

$136 - $226/hr

Join Stryker in a leadership role overseeing manufacturing operations within a regulated medical device environment. This position is responsible for leading manufacturing, planning, purchasing ...

Banner Health

Biomedical IoMT Specialist

Chandler, AZ · On-site

This role is integral to Banner Health's medical device security program, ensuring compliance and ... Operations (experience with information technology related to workstations, networking, and ...

Banner Health

Biomedical IoMT Specialist

Chandler, AZ · On-site

This role is integral to Banner Health's medical device security program, ensuring compliance and ... Operations (experience with information technology related to workstations, networking, and ...

Hanger, Inc.

QA/QC Engineer II

Phoenix, AZ

$71K - $92K/yr

... operational equipment is timely calibrated and validated. Minimum: * Bachelor's degree in ... Experience in manufacturing of medical device with electronic components is preferred. * Broad ...

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All JobsMedical Device Operations JobsMedical Device Operations Jobs in Phoenix, AZ

Medical Device Operations information

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$11

$26

$52

How much do medical device operations jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical device operations in Phoenix, AZ is $26.06, according to ZipRecruiter salary data. Most workers in this role earn between $17.64 and $30.10 per hour, depending on experience, location, and employer.

What is medical device operations?

Medical device operations refer to the processes and activities involved in the manufacturing, assembly, quality control, supply chain management, and distribution of medical devices. This field ensures that devices are produced efficiently, meet regulatory standards, and are delivered safely to healthcare providers and patients. Operations teams collaborate with engineering, quality assurance, and regulatory departments to maintain compliance and optimize production workflows. Their work is crucial for ensuring that medical devices are safe, effective, and readily available for patient care.

What are the key skills and qualifications needed to thrive in medical device operations?

To thrive in Medical Device Operations, you need a solid understanding of regulatory compliance, quality assurance, and supply chain management, often supported by a degree in engineering, life sciences, or business. Familiarity with quality management systems (QMS), FDA regulations, and software like ERP systems is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring compliance. These competencies are vital for delivering safe, high-quality medical devices efficiently and in accordance with rigorous industry standards.

What are some common challenges faced by professionals in medical device operations, and how can they be addressed?

Professionals in Medical Device Operations often face challenges related to maintaining strict regulatory compliance, ensuring product quality, and managing cross-functional communication between manufacturing, quality assurance, and regulatory teams. Staying up to date with changing FDA or international regulations is essential, and frequent documentation or process audits can be demanding. Building strong organizational habits, leveraging digital tracking tools, and fostering open communication channels with other departments can help address these challenges and ensure smooth operations.

What is the difference between Medical Device Operations vs Medical Device Quality Assurance?

AspectMedical Device OperationsMedical Device Quality Assurance
Primary FocusManaging manufacturing, supply chain, and product deploymentEnsuring product quality, compliance, and safety standards
Required CertificationsRegulatory knowledge, manufacturing certificationsQuality management certifications, ISO standards
Work EnvironmentManufacturing plants, supply chain settingsQuality labs, compliance departments
Industry UsageUsed across production and logistics teamsUsed within quality control and regulatory teams

Medical Device Operations and Medical Device Quality Assurance roles often overlap but focus on different aspects of the product lifecycle. Operations centers on manufacturing and logistics, while Quality Assurance emphasizes compliance and safety. Both roles require regulatory knowledge and are essential in the medical device industry.

What are the most commonly searched types of Medical Device Operations jobs in Phoenix, AZ?

The most popular types of Medical Device Operations jobs in Phoenix, AZ are:

What are popular job titles related to Medical Device Operations jobs in Phoenix, AZ?

For Medical Device Operations jobs in Phoenix, AZ, the most frequently searched job titles are:

What job categories do people searching Medical Device Operations jobs in Phoenix, AZ look for?

The top searched job categories for Medical Device Operations jobs in Phoenix, AZ are:

Medical Device Operations jobs near you
Infographic showing various Medical Device Operations job openings in Phoenix, AZ as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $54,201 per year, or $26.1 per hour.

Staff Quality Engineer - Product Development, Tempe, AZ - (IK)

Central Business Solutions, Inc

Tempe, AZ • On-site

$110 - $115/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

Staff Quality Engineer - Product Development, Tempe, AZ - (IK)
  • Tempe, Arizona

Job Responsibilities:

Technical leadership skills including an understanding of medical device operations (e.g., medical device manufacturing, process development, quality assurance) and chemical and pharmaceutical operations (e.g., drug product manufacturing, analytical testing, process development and quality assurance)

Ability to create, support, review, and investigate analytical test methods used to support pharmaceutical combination devices.

The ability to create, support, review chemistry, manufacturing, and controls device submissions

Participates as team leader or as an active member of the team to meet company objectives and ensure department responsibilities are completed

Leads development of risk assessments and test method activities (e.g., development and validation for physical and analytical test methods)

Leads component qualifications, design validation, design verification, drug stability and process validation

Leads product investigations

Ability to make and present risked based decisions

Supports translation of design inputs into manufacturing control plans

Develop and implement procedures to comply with corporate and industry standards.

Coordinates and/or directs all aspects of product development activity related to a product line

Leads development of risk assessments and test methods

Quality engineering representation on Product Development and Design Review teams

Prepare and present project updates and technical discussions

Participate in project planning, budgeting, scheduling, and tracking

Support internal and external supplier audits

Provide support to the regulatory department in writing technical submissions

Complies with company procedures and policies, government regulations

Actively participates in training and providing input to training of employees on division procedures and policies

Ability to travel for business, project, and issues approximately up to 25% of time.

Other duties and projects, as assigned

Required Education and Experience:

BS in Engineering, Biological Science, or a related engineering field (Masters or Ph.D preferred). Fields of study include Chemical Engineering, Bioengineering, Pharmacy, or Biochemistry

Minimum of eight years of experience in engineering or Quality engineering experience within the medical device, pharmaceutical, or equivalent industry

Extensive proven understanding of design controls in development stage

Pharmaceutical or combination product experience

Required Qualifications:

Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)

Ability to lead creation of risk management files

Ability to develop solutions with business impact

Advanced statistical and risk assessment techniques

Working knowledge of test method (development and validation), equipment qualifications, process and design validation, risk assessment techniques, and component qualification methodologies

Ability to make and present risk-based decisions

Strong interpersonal skills

Ability to analyze and optimize manufacturing and quality systems

Product, design & prototyping

Ability to create and provide training

Problem solving ability

Ability to create, review and coordinate test protocols and reports

Ability to generate engineering proposals

Oral and written presentation skills

Ability to lead cross functional teams

Understanding of regulatory requirements including ISO 13485, ISO 14971, 21 CFR 210/211/820 , ICH Guidelines

Skills and Certifications

Drug Device delivery combination products

Compensation

Base Salary -USD $110,000 to $115,000

Candidate Details

Full-time

Benefits -Full

Relocation Assistance Available -Possible for ideal candidate

Ideal Candidate

8+ years experience in New Product Development of combination devices

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