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Associate Medical Device Labeling Jobs in Raleigh, NC

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · Hybrid

$40 - $42/hr

Medical Device Vigilance Professionals Location: Raleigh, NC Pay Rate: $40-42/HR on W2 Full time - fully Onsite - 3 days a week in office requirement (flexible days) for 6 months, WFH 2 days a week.

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · Hybrid

$40 - $42/hr

Medical Device Vigilance Professionals Location: Raleigh, NC Pay Rate: $40-42/HR on W2 Full time - fully Onsite - 3 days a week in office requirement (flexible days) for 6 months, WFH 2 days a week.

IQVIA

Associate Labeling Strategy Director

Durham, NC · On-site

$103K - $288K/yr

The Role: IQVIA is seeking a Associate Director of Regulatory Labeling Strategy to support new ... Proven ability in medical/technical writing. * Labeling experience (CCDS, US, EU, UK, other major ...

IQVIA

Associate Labeling Strategy Director

Durham, NC · On-site

$103K - $288K/yr

The Role: IQVIA is seeking a Associate Director of Regulatory Labeling Strategy to support new ... Proven ability in medical/technical writing. * Labeling experience (CCDS, US, EU, UK, other major ...

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

... the medical device industry. Our team supports start-ups, mid-sized private companies, and the ... Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to ...

AA2IT

Associate Director Quality Assurance

Raleigh, NC · On-site

$45 - $50/hr

Quality activities for medical device manufacturing and Design & Development activities throughout all stages of the device development process (e.g. general Product Development / Design Control ...

AA2IT

Associate Director Quality Assurance

Raleigh, NC · On-site

$45 - $50/hr

Quality activities for medical device manufacturing and Design & Development activities throughout all stages of the device development process (e.g. general Product Development / Design Control ...

IQVIA

Associate Director, Medical Reviewer

Durham, NC · Remote

$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 ...

IQVIA

Associate Director, Medical Reviewer

Durham, NC · Remote

$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 ...

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All JobsAssociate Medical Device Labeling JobsAssociate Medical Device Labeling Jobs in Raleigh, NC

Associate Medical Device Labeling information

See Raleigh, NC salary details

$12

$29

$92

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

Medical Device Vigilance professionals

AA2IT

Raleigh, NC • Hybrid

$40 - $42/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Medical Device Vigilance Professionals

Location: Raleigh, NC

Pay Rate: $40-42/HR on W2

Full time - fully Onsite - 3 days a week in office requirement (flexible days) for 6 months, WFH 2 days a week.

Responsible for all tasks related to the collection, processing, follow up and regulatory reporting of adverse events (AEs), serious AEs from clinical trials (SAEs), adverse events of interest (AEIs) and pregnancy reports for all of Merz Aesthetics marketed and investigational products.

This position will routinely process all types of reports for all categories of products (medical device, cosmetic and OTC products).

Major Duties Description:

  • Post Marketing Adverse Event Processing
  • Clinical Study SAE Processing
  • On Time Submission of AE Reports
  • Evaluation of Individual AE Reports and Safety Data
  • Literature Reviews
  • Safety Database Proficiency
  • Review and Update of Departmental Documents
  • Provides Training Regarding AE Reporting
  • Audit Support
  • Supports Regional Safety/Vigilance
  • Collaborate with Other Global Functions

Technical & Functional Skills:

  • Thorough knowledge and experience in all aspects of safety reporting for clinical trials and marketed products – both drugs and medical devices.
  • Strong knowledge and experience with validated safety databases (Argus, ARISg, SIAB, etc.). This also includes MedDRA, WHODrug, and IMDRF coding.
  • Must work effectively/collaboratively in a fast-paced yet efficient team environment with individuals at all levels within an organization.
  • Strong knowledge of FDA and EU regulations governing clinical safety and vigilance.
  • Strong organizational and project management skills.
  • Strong verbal and written communication skills.

Minimum Qualifications:

  • Bachelor's degree in a science or health care-related field or RN/PharmD
  • 5+ years of experience in drug safety or medical device vigilance (preferred) in an industry setting or equivalent

Preferred Qualifications:

  • Direct health care experience with injectable products highly desired
  • Knowledge and experience with document management systems (EDMS, eTMF, etc.)
  • Experience in vendor management
  • Demonstrates relationship building and problem-solving skills

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