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Associate Medical Device Labeling Jobs in Raleigh, NC

IQVIA, Inc.

Associate Director, Medical Reviewer

Durham, NC · On-site

$115K - $322K/yr

Associate Director, Medical Review (MLR) Location : Home-based in USA Job Overview: IQVIA Pharma ... Advanced knowledge of pharmaceutical and medical device guidelines and regulations. * Experience on ...

Laborie

Associate Territory Manager

Raleigh, NC · On-site

Demonstrate professionalism and discipline in a regulated medical device environment by managing territorylogisticsand travel efficiently, adhering to compliance and quality requirements ...

Aerogen

Senior Director of Quality

Morrisville, NC · On-site

$120 - $160/hr

... testing, labeling, and other quality activities. * Oversee quality investigations performed ... Collaborate with the development team working with medical device suppliers, CDMOs and CMOs.

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Associate Medical Device Labeling information

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

As of Sep 7, 2026, the average hourly pay for associate medical device labeling in Raleigh, NC is $29.67, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $38.08 per hour, depending on experience, location, and employer.

What is an associate medical device labeling?

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?

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 are some common challenges faced by associate medical device labeling, 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.
Associate Medical Device Labeling jobs near you

Associate Director, Medical Reviewer

IQVIA, Inc.

Durham, NC • On-site

$115K - $322K/yr

Full-time

Re-posted 9 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services

Job description

Job Level: Associate Director, Medical Review (MLR)
Location: Home-based in USA
Job Overview:
IQVIA Pharma Review provides outsourced medical copy review and approval services and advisory services to the pharmaceutical industry.
As a Final Medical Content Approver, you will act as the primary medical and scientific point of contact providing final approval and expert advice to our clients in line with the requirements of the FDA (FDCA) / PhRMA / FTC for pharmaceuticals and medical devices on assets for clients. You will be expected to be part of the relevant content review teams eg Project/ Product Review Teams (PRT).
In this role and as part of the Medical Quality and Compliance team you will be working alongside and as part of the IQVIA Pharma Review Account Teams to deliver a seamless and consistent approach to content approval and consultative compliance advice to the US based clients and business and provide some account management services.
In addition, you will be expected to support Business Development in discussions with potential new clients, provide RFP input when required, support internal Pharma Review (and IQVIA) with expert knowledge of FDA requirements aligned to pharmaceutical materials
The Account Teams are comprised of a group of reviewers that perform scientific, technical and quality checks of materials for scientific accuracy, substantiation, quality and relevant pharmaceutical regulations and codes.
This is a remote role but may require onsite visits to clients.
Job Responsibilities:
  • Represent Medical Affairs on the content review committee as the lead Medical Cotnet Reviewer / Approver of promotional and non-promotional materials and activities (eg congresses).
  • Provide expert final approval services to Pharma Review clients which include the approval of relevant assets in line with client's strategy, expectations and SOPs
  • Effectively collaborate with Commercial, Regulatory, and Legal business partners to provide strategic input and drive alignment as required.
  • Advise on approval processes and best practices
  • Act as an internal escalation point for review team on complex jobs
  • Actively participate in and lead internal training for the US market
  • Maintain up-to-date knowledge of advertising regulations from FDA/ PhRMA, healthcare landscape, and trends in MLR eg AI) including attending relevant training, and share relevant outputs
  • Medical approver representative at client meetings as needed
  • Active involvement in recruitment of reviewers and onboarding new starters as required.
  • Coaching and mentoring of less experienced members of the team in technical and leadership skills
  • Work with Compliance Team on internal and client audits as required
  • Manage time proactively and track work hours in time-sheet in line with operations guidance.
  • Provide 'second opinions' where appropriate.
  • Escalates issues to medical director where appropriate.
  • Be a leader and role model for core IQVIA compliance values
  • Work with internal IQVIA functions such as business development to contribute to the expansion of the US market
  • Currently no line management but may be required in future

Qualifications:
  • An advanced science or medical degree (PharmD, PhD, MD, PhD) strongly preferred or equivalent experience
  • At least 3-5 years of direct US promotional/medical review experience and be comfortable working independently with minimal oversight.
  • Demonstrated ability to critically analyze research design, methods, and outcome measures.
  • Advanced knowledge of pharmaceutical and medical device guidelines and regulations.
  • Experience on an approval system like Veeva Promomats and/ or Aprimo desorable

#LI-Remote
#LI-NITINMAHAJAN
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $115,900.00 - $322,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

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At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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