Evaluate product labeling, product claims, advertising, specifications, and changes for regulatory ... Bachelor's degree, and minimum 4 years of Regulatory Affairs experience in the medical device ...
Evaluate product labeling, product claims, advertising, specifications, and changes for regulatory ... Bachelor's degree, and minimum 4 years of Regulatory Affairs experience in the medical device ...
Quality Inspector Metrology
Phoenix, AZ · On-site
Medical
Dental
Vision
Life
Retirement
PTO
Perform routine dimensional and visual inspections of molded medical device components on the ... Ensure traceability and proper labeling of inspected product. * Ensure inspections are performed in ...
Quick apply
Quality Inspector Metrology
Phoenix, AZ · On-site
Medical
Dental
Vision
Life
Retirement
PTO
Perform routine dimensional and visual inspections of molded medical device components on the ... Ensure traceability and proper labeling of inspected product. * Ensure inspections are performed in ...
Quality Inspector Metrology
Phoenix, AZ · On-site
Medical
Dental
Vision
Life
Retirement
PTO
Perform routine dimensional and visual inspections of molded medical device components on the ... Ensure traceability and proper labeling of inspected product. * Ensure inspections are performed in ...
Quick apply
Quality Inspector Metrology
Phoenix, AZ · On-site
Medical
Dental
Vision
Life
Retirement
PTO
Perform routine dimensional and visual inspections of molded medical device components on the ... Ensure traceability and proper labeling of inspected product. * Ensure inspections are performed in ...
Sr Hardware Engineer
Arizona City, AZ · On-site
$116.60 - $194.40/hr
Medical
Life
... medical device products to patients around the world. Our team focuses on packaging, labeling, and distribution operations, working hands‑on with advanced, high‑volume equipment to ensure ...
Sr Hardware Engineer
Arizona City, AZ · On-site
$116.60 - $194.40/hr
Medical
Life
... medical device products to patients around the world. Our team focuses on packaging, labeling, and distribution operations, working hands‑on with advanced, high‑volume equipment to ensure ...
... Medical Device Reporting (MDR) submission requirements. · Review labeling and promotional materials to ensure compliance with applicable regulations. · Participate in internal and external audits ...
New
... Medical Device Reporting (MDR) submission requirements. · Review labeling and promotional materials to ensure compliance with applicable regulations. · Participate in internal and external audits ...
New
QA/QC Engineer II
Phoenix, AZ · On-site
$71K - $92K/yr
Medical
Dental
Vision
Retirement
PTO
Through its Products & Services segment, Hanger distributes branded and private label O&P devices ... Experience in manufacturing of medical device with electronic components is preferred. * Broad ...
QA/QC Engineer II
Phoenix, AZ · On-site
$71K - $92K/yr
Medical
Dental
Vision
Retirement
PTO
Through its Products & Services segment, Hanger distributes branded and private label O&P devices ... Experience in manufacturing of medical device with electronic components is preferred. * Broad ...
... Medical Device Reporting (MDR) submission requirements. • Review labeling and promotional materials to ensure compliance with applicable regulations. • Participate in internal and external audits ...
New
... Medical Device Reporting (MDR) submission requirements. • Review labeling and promotional materials to ensure compliance with applicable regulations. • Participate in internal and external audits ...
New
QA/QC Engineer II
Phoenix, AZ · On-site
$71K - $92K/yr
Medical
Dental
Vision
Retirement
PTO
Through its Products & Services segment, Hanger distributes branded and private label O&P devices ... Experience in manufacturing of medical device with electronic components is preferred. * Broad ...
QA/QC Engineer II
Phoenix, AZ · On-site
$71K - $92K/yr
Medical
Dental
Vision
Retirement
PTO
Through its Products & Services segment, Hanger distributes branded and private label O&P devices ... Experience in manufacturing of medical device with electronic components is preferred. * Broad ...
... Medical Device Reporting (MDR) submission requirements. · Review labeling and promotional materials to ensure compliance with applicable regulations. · Participate in internal and external audits ...
New
Quick apply
... Medical Device Reporting (MDR) submission requirements. · Review labeling and promotional materials to ensure compliance with applicable regulations. · Participate in internal and external audits ...
New
Sr Hardware Engineer
Arizona City, AZ · On-site
$116.60 - $194.40/hr
Medical
Life
Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging, labeling, and ...
Sr Hardware Engineer
Arizona City, AZ · On-site
$116.60 - $194.40/hr
Medical
Life
Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging, labeling, and ...
Regulatory Affairs Leader
Flagstaff, AZ · On-site
... including labeling, promotional advertising, and other regulatory compliance areas * Ensure ... Bachelor's degree and at least 8 years of experience in medical device Regulatory Affairs
New
Regulatory Affairs Leader
Flagstaff, AZ · On-site
... including labeling, promotional advertising, and other regulatory compliance areas * Ensure ... Bachelor's degree and at least 8 years of experience in medical device Regulatory Affairs
New
Review and approve advertising/marketing material, and product labeling to ensure compliance with ... Experience and knowledge of Canadian Medical Device Regulations, MDSAP, and ISO Standards;
Review and approve advertising/marketing material, and product labeling to ensure compliance with ... Experience and knowledge of Canadian Medical Device Regulations, MDSAP, and ISO Standards;
Review and approve advertising/marketing material, and product labeling to ensure compliance with ... Experience and knowledge of Canadian Medical Device Regulations, MDSAP, and ISO Standards;
Review and approve advertising/marketing material, and product labeling to ensure compliance with ... Experience and knowledge of Canadian Medical Device Regulations, MDSAP, and ISO Standards;
Review and approve advertising/marketing material, and product labeling to ensure compliance with ... Experience and knowledge of Canadian Medical Device Regulations, MDSAP, and ISO Standards;
Quick apply
Review and approve advertising/marketing material, and product labeling to ensure compliance with ... Experience and knowledge of Canadian Medical Device Regulations, MDSAP, and ISO Standards;
Sr Hardware Engineer
Mesa, AZ · On-site
$109K - $146K/yr
Medical
Life
Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging, labeling, and ...
Sr Hardware Engineer
Mesa, AZ · On-site
$109K - $146K/yr
Medical
Life
Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging, labeling, and ...
Sr Hardware Engineer
$109K - $146K/yr
Medical
Life
Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging, labeling, and ...
Sr Hardware Engineer
$109K - $146K/yr
Medical
Life
Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging, labeling, and ...
Sr Hardware Engineer
Arizona City, AZ · On-site
$111K - $148K/yr
Medical
Life
Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging, labeling, and ...
Sr Hardware Engineer
Arizona City, AZ · On-site
$111K - $148K/yr
Medical
Life
Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging, labeling, and ...
Sr. R&D Engineer
Tempe, AZ · On-site
$101K - $139K/yr
... labeling inputs, and production support documentation are complete. * Maintain a working knowledge of applicable government and industry quality assurance codes, standards, and medical device design ...
Sr. R&D Engineer
Tempe, AZ · On-site
$101K - $139K/yr
... labeling inputs, and production support documentation are complete. * Maintain a working knowledge of applicable government and industry quality assurance codes, standards, and medical device design ...
... med-spas) who can prescribe and dispense directly from a pharmacy. * White-label partners ... device, peptides/GLP-1, med-spa, aesthetics, longevity/wellness, or healthcare sales. * A track ...
Quick apply
... med-spas) who can prescribe and dispense directly from a pharmacy. * White-label partners ... device, peptides/GLP-1, med-spa, aesthetics, longevity/wellness, or healthcare sales. * A track ...
QC Inspector - 1st Shift
Scottsdale, AZ · On-site
... medical device company. Essential Duties and Responsibilities: * Perform inspections of purchased ... Ensures appropriate labeling, storage and handling of product and materials throughout the ...
QC Inspector - 1st Shift
Scottsdale, AZ · On-site
... medical device company. Essential Duties and Responsibilities: * Perform inspections of purchased ... Ensures appropriate labeling, storage and handling of product and materials throughout the ...
Medical Device Labeling information
See Arizona salary details
$14.74 is the 25th percentile. Wages below this are outliers.
$12.10 - $19.08
66% of jobs
$19.08 - $26.07
6% of jobs
$28.98 is the 75th percentile. Wages above this are outliers.
$26.07 - $33.05
6% of jobs
$33.05 - $40.04
7% of jobs
$40.04 - $47.02
5% of jobs
$47.02 - $54.01
5% of jobs
$54.01 - $60.99
1% of jobs
$60.99 - $67.98
0% of jobs
$67.98 - $74.96
0% of jobs
$74.96 - $81.95
1% of jobs
$81.95 - $88.93
1% of jobs
$12
$28
$88
How much do medical device labeling jobs pay per hour?
As of Aug 16, 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?
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 does a medical device labeling do?
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 key skills and qualifications needed to thrive in medical device labeling?
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 most commonly searched types of Medical Device Labeling jobs in Arizona?
The most popular types of Medical Device Labeling jobs in Arizona are:
What are popular job titles related to Medical Device Labeling jobs in Arizona?
For Medical Device Labeling jobs in Arizona, the most frequently searched job titles are:
- Press Operator
- Medical Device Quality Assurance
- Freelance Medical Device Quality Assurance
- Director Medical Device Product Development
- Hourly Hp Indigo Digital Press Operator
- Medical Device Packaging
- Director Medical Device Quality Assurance
- Hp Indigo Digital Press Operator
- Internship Hp Indigo Digital Press Operator
- Contract Medical Device Auditor
What job categories do people searching Medical Device Labeling jobs in Arizona look for?
The top searched job categories for Medical Device Labeling jobs in Arizona are:
Full-time
Posted 11 days ago
W. L. Gore & Associates rating
8.9
Based on 80 frontline employees who took The Breakroom Quiz
8th of 540 rated manufacturers
Job description
Senior Regulatory Affairs Professional
Req Id: 2053
State/Province: Arizona
Business: Gore Medical Products
Category: Clinical & Regulatory
Sub-Category: Regulatory & Quality
Work Arrangement: Remote
Posting Start Date: 8/3/26
Posting End Date: 8/18/26
About the Role
We are looking for a Senior Regulatory Affairs Product Associate to join our team within the Peripheral Business Group. In this role, you will develop and execute regulatory strategies to achieve and maintain global marketing approvals for new, modified, and existing implantable medical devices. You will lead the preparation, coordination, and execution of global regulatory submissions while partnering with cross-functional teams throughout the product development and product lifecycle.
This is a remote position, and you can work from home in most locations within the United States.
Responsibilities
Required Qualifications
Desired Qualifications
This position offers a remote work arrangement in the country from which the Associate is employed. Eligibility is dependent on the responsibilities of the role and business needs, and the Associate must agree to comply with Gore's work arrangement policies.
*Note: In the United States, restrictions exist for remote work from Alaska, Hawaii and Rhode Island.
Information at a Glance
Req Id: 2053
State/Province: Arizona
Business: Gore Medical Products
Category: Clinical & Regulatory
Sub-Category: Regulatory & Quality
Work Arrangement: Remote
Posting Start Date: 8/3/26
Posting End Date: 8/18/26
About the Role
We are looking for a Senior Regulatory Affairs Product Associate to join our team within the Peripheral Business Group. In this role, you will develop and execute regulatory strategies to achieve and maintain global marketing approvals for new, modified, and existing implantable medical devices. You will lead the preparation, coordination, and execution of global regulatory submissions while partnering with cross-functional teams throughout the product development and product lifecycle.
This is a remote position, and you can work from home in most locations within the United States.
Responsibilities
- Partner with technical, regulatory affairs, research associates, and product specialists to develop strategies and approaches for obtaining and maintaining regulatory approvals
- Coordinate and lead activities and timelines with applicable functional groups to complete regulatory submissions
- Evaluate product labeling, product claims, advertising, specifications, and changes for regulatory compliance and determine applicable regulatory requirements and submission needs
- Interact closely with and counsel functional groups in the business to provide regulatory guidance and review of their activities, including recommendations regarding regulatory requirements and potential risks
- Integrate into the Regulatory Affairs team to facilitate collaborative and consistent regulatory counsel to product functional groups
- Represent Regulatory Affairs in quality system audits by external agencies
- Assist with post-market compliance requirements, including required regulatory reporting and lifecycle management activities
- Identify regulatory risks and recommend appropriate regulatory strategies, submission requirements, and paths forward for assigned products and projects
- Maintain compliance with training expectations as required for this position
Required Qualifications
- Bachelor's degree, and minimum 4 years of Regulatory Affairs experience in the medical device industry
- Experience formulating and implementing regulatory strategies and writing comprehensive regulatory documents
- Knowledge of FDA and international regulations related to Class II and Class III implantable medical devices
- Demonstrated success regarding the assessment of proposed changes to medical device design, specifications, materials, manufacturing methods or equipment, supplied components, packaging, or sterilization and determining associated regulatory requirements
- Successful experience leading or supporting submissions associated with device modifications and manufacturing process modifications
- Experience proactively identifying necessary submission content, assessing project documentation for completeness and regulatory compliance, including compliance with international standards
- Strong communication (oral, written, and interpersonal) skills, including the ability to effectively communicate regulatory requirements and collaborating effectively to cross-functional teams
- Demonstrated ability to analyze regulatory issues, assess regulatory risks, and recommend appropriate regulatory approaches
- Strong project management and organizational skills
- Ability to travel up to 15%
Desired Qualifications
- Experience preparing or supporting submissions for PMA, IDE, or other Class III medical device products
- Experience preparing regulatory submissions for Class III medical devices under the European Medical Device Regulation (EU MDR) or another Tier 1 regulatory authority
- Experience with regulatory requirements for combination (drug/device) products
This position offers a remote work arrangement in the country from which the Associate is employed. Eligibility is dependent on the responsibilities of the role and business needs, and the Associate must agree to comply with Gore's work arrangement policies.
*Note: In the United States, restrictions exist for remote work from Alaska, Hawaii and Rhode Island.
Information at a Glance
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