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Associate Medical Device Labeling Jobs (NOW HIRING)

CYNET SYSTEMS

Labeling Specialist

Cupertino, CA · On-site

$62 - $67/hr

Knowledge of domestic and international medical device regulatory requirements for product labeling and unique device identification (e.g. 21 CFR 801 and EU MDR). * Knowledge of quality management ...

JenaValve

Specialist, Labeling Control

Irvine, CA · On-site

$82K/yr

Review and approve labeling to ensure compliance with ISO 15223-1 (medical device symbols), ISO 20417 (information supplied by the manufacturer), ISO 5840 (cardiovascular implant labeling), and EU ...

Noblesoft Technologies

Labeling Analyst

Irving, TX · On-site

... Medical device Labeling and packaging re-design and test methods to improve label readability, barcode placement, and manufacturing efficiency -Participate in investigations related to labeling ...

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How much do associate medical device labeling jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for associate medical device labeling in the United States is $30.53, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $39.18 per hour, depending on experience, location, and employer.

What are some common challenges faced by Associate Medical Device Labeling professionals, and how can they be addressed?

Associate Medical Device Labeling professionals often encounter challenges such as keeping up with evolving regulatory requirements across different countries, ensuring accuracy and clarity in complex technical information, and coordinating input from multiple departments like regulatory affairs, engineering, and marketing. Addressing these challenges involves staying updated on global labeling standards, developing strong attention to detail, and building effective communication and collaboration skills. Leveraging project management tools and regularly participating in training can also help manage these complexities and ensure timely, compliant labeling deliverables.

What are Associate Medical Device Labeling professionals?

Associate Medical Device Labeling professionals are responsible for creating, reviewing, and maintaining the labeling and packaging materials for medical devices. Their work ensures that all product information, instructions, and regulatory warnings are accurate, clear, and compliant with industry regulations. They collaborate closely with regulatory affairs, quality assurance, and product development teams to make sure that labels meet local and international standards. This role is critical in helping ensure patient safety and regulatory approval of medical devices.

What are the key skills and qualifications needed to thrive as an Associate Medical Device Labeling Specialist, and why are they important?

To thrive as an Associate Medical Device Labeling Specialist, you need a strong understanding of regulatory requirements, attention to detail, and experience in technical writing, often supported by a degree in life sciences or a related field. Familiarity with labeling software, document management systems, and knowledge of FDA or EU MDR regulations are typically required. Excellent communication, collaboration, and organizational skills set top performers apart in this position. These skills are crucial to ensure label accuracy, regulatory compliance, and patient safety in a highly regulated industry.
What cities are hiring for Associate Medical Device Labeling jobs? Cities with the most Associate Medical Device Labeling job openings:
What are the most commonly searched types of Medical Device Labeling jobs? The most popular types of Medical Device Labeling jobs are:
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Associate Medical Device Labeling jobs near you
Quality Compliance/Labeling Specialist (Medical Device)

Quality Compliance/Labeling Specialist (Medical Device)

Adecco

Cupertino, CA

$57 - $67/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Job description

Quality Compliance/Labeling Specialist

Adecco Healthcare & Life Sciences is hiring for a notable global medical device organization recognized for its innovation in consumer and clinical technology products, quality-driven design standards, and strong commitment to global regulatory compliance.

This is a contract opportunity for a Labeling Specialist supporting global product labeling, Instructions for Use (IFU) development, and regulatory compliance activities across domestic and international markets.

Pay: Up to 67/hr depending on relevant experience level

Duration: 6 months temp to hire

Location: CUPERTINO, CA

The Opportunity

Join a cross-functional regulatory and quality team responsible for ensuring accurate, compliant, and globally aligned product labeling for medical devices. In this role, you will support the creation, review, and maintenance of Instructions for Use (IFUs), marketing claims, and labeling documentation while ensuring adherence to global regulatory requirements.

This position plays a key role in maintaining compliance with evolving domestic and international medical device labeling standards while collaborating closely with Regulatory Affairs, Quality, Engineering, and Marketing teams.

Key Responsibilities

  • Lead the development and maintenance of Instructions for Use (IFUs) ensuring compliance with global regulatory requirements

  • Review and approve product labeling to ensure accuracy, completeness, and regulatory alignment

  • Manage labeling-related marketing claims and coordinate cross-functional approvals

  • Support internal review processes for marketing and post-market labeling materials

  • Establish and maintain systems for physical and electronic labeling controls

  • Ensure labeling documentation remains compliant with global standards and evolving regulatory requirements

  • Partner with Regulatory Affairs to incorporate country-specific labeling requirements and translations for international markets

  • Participate in design control and change control processes related to product updates, enhancements, and regulatory changes

Minimum Qualifications

  • Bachelor’s degree or equivalent relevant experience

  • 2–5 years of experience in medical device labeling or regulatory labeling support

  • Strong understanding of global medical device labeling regulations, including 21 CFR 801 and EU MDR

  • Knowledge of Quality Management Systems (QMS), including design control, document control, and regulatory approval processes

  • Excellent written and verbal communication skills

  • Strong interpersonal skills with experience working across multiple cross-functional teams

  • Highly organized with strong attention to detail and time management skills

  • Ability to work independently and manage multiple priorities

  • Technical writing experience preferred

Why Work for Adecco Healthcare & Life Sciences?

Adecco Healthcare & Life Sciences connects talented professionals with leading organizations across the medical device, biotechnology, pharmaceutical, and diagnostics industries. We specialize in both contract and direct hire opportunities that support career growth and long-term development.

We offer:

  • Access to top-tier medical device and life sciences opportunities

  • Weekly pay options for applicable roles

  • Comprehensive medical, dental, vision, and 401(k) benefits

  • Dedicated recruiter support throughout your assignment

  • Opportunities across global, regulated life sciences organizations


Pay Details: $57.00 to $67.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.