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Home Based Labelling Jobs in Raleigh, NC (NOW HIRING)

Teleflex

Global Labeling Systems Lead

Morrisville, NC · On-site

... the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™ ... This position can be based at our Morrisville, NC, Maple Grove, MN, or Athlone, Ireland office.

Assisting Hands

Experienced PCA's

Cary, NC · On-site

$14 - $16/hr

One (1) year experience in the home or long-term care setting is preferred. Reports to: Staffing ... In the presence of the client, reading the label, opening the container, removing a prescribed ...

Lowe's

Warehouse Associate II

Durham, NC

$15.50 - $18.25/hr

Trained and performs tasks in cross-functional areas, such as picking, pulling, labeling, shipping ... over 1,700 home improvement stores and employs approximately 300,000 associates. Based in ...

Lowe's

Warehouse Associate II

Durham, NC

$15.50 - $18.25/hr

Trained and performs tasks in cross-functional areas, such as picking, pulling, labeling, shipping ... over 1,700 home improvement stores and employs approximately 300,000 associates. Based in ...

PharMerica

Pharmacy Technician

Raleigh, NC · On-site

$17 - $20.75/hr

Labels products appropriately, including cautionary or auxiliary labels * Participates in the ... Services facility-based medication dispensing machines (e.g., RxNow) * Performs other tasks as ...

BrightSpring

Pharmacy Technician / Overnight

Raleigh, NC

$17 - $20.75/hr

Labels products appropriately, including cautionary or auxiliary labels * Participates in the ... Services facility-based medication dispensing machines (e.g., RxNow) * Performs other tasks as ...

PharMerica

Pharmacy Technician / Overnight

Raleigh, NC · On-site

$17 - $20.75/hr

Labels products appropriately, including cautionary or auxiliary labels * Participates in the ... Services facility-based medication dispensing machines (e.g., RxNow) * Performs other tasks as ...

PharMerica

Pharmacy Technician / Overnight

Raleigh, NC

$17 - $20.75/hr

Labels products appropriately, including cautionary or auxiliary labels * Participates in the ... Services facility-based medication dispensing machines (e.g., RxNow) * Performs other tasks as ...

PharMerica

Pharmacy Technician

Raleigh, NC

$17 - $20.75/hr

Labels products appropriately, including cautionary or auxiliary labels * Participates in the ... Services facility-based medication dispensing machines (e.g., RxNow) * Performs other tasks as ...

BrightSpring

Pharmacy Technician

Raleigh, NC

$17 - $20.75/hr

Labels products appropriately, including cautionary or auxiliary labels * Participates in the ... Services facility-based medication dispensing machines (e.g., RxNow) * Performs other tasks as ...

Closets By Design Raleigh

CNC Operator

Raleigh, NC

$18 - $21/hr

... home offices, and garage cabinetry. Unlike general metalworking roles, this position focuses ... Operate CNC routers (such as the HOMAG) to cut, drill, and route panels based on specific job ...

Duke University

Lab Research Analyst I

Durham, NC

... Home Care and Hospice, Duke Health and Wellness, and multiple affiliations. Be You. The Bryan Brain ... Prepare, label, and track biological specimens including frozen tissue, FFPE tissue, blocks, slides ...

Duke University

Lab Research Analyst I

Durham, NC · On-site

... Home Care and Hospice, Duke Health and Wellness, and multiple affiliations. Be You. The Bryan Brain ... Prepare, label, and track biological specimens including frozen tissue, FFPE tissue, blocks, slides ...

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Home Based Labelling information

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How much do home based labelling jobs pay per hour?

As of May 30, 2026, the average hourly pay for home based labelling in Raleigh, NC is $15.95, according to ZipRecruiter salary data. Most workers in this role earn between $14.04 and $17.55 per hour, depending on experience, location, and employer.

What is a Home Based Labelling job?

A Home Based Labelling job involves tagging, categorizing, or labeling data, products, or images from home. Tasks may include adding descriptions to images, labeling product packages, or sorting data for machine learning models. These jobs are often part of remote work opportunities offered by companies looking to organize and categorize information efficiently. No specialized skills may be required for entry-level roles, but attention to detail and consistency are crucial. Pay can vary based on the complexity and volume of the work assigned.

What are the key skills and qualifications needed to thrive in the Home Based Labelling position, and why are they important?

To thrive in a Home Based Labelling role, attention to detail, strong organizational skills, and the ability to follow precise instructions are essential, often requiring a high school diploma or equivalent. Familiarity with basic computer applications, labelling software, or inventory management systems is typically advantageous. Excellent time management, self-motivation, and reliability are key soft skills that help individuals excel when working independently from home. These abilities ensure accurate completion of tasks, efficient workflow, and dependability in a remote setting.

What does a typical day look like for someone in a Home Based Labelling position?

In a Home Based Labelling role, your day usually involves reviewing instructions provided by your employer, accurately applying labels to products or data files, and maintaining clear records of completed work. You may be required to receive materials shipped to your home, use specified labelling software, or upload documentation via an online portal. Communication with supervisors is often handled through email or project management tools to address any questions or updates. The work structure is generally independent, allowing for a flexible schedule, but adhering to deadlines and quality standards is crucial for ongoing success. This role is ideal for individuals who enjoy detail-oriented, repetitive tasks in a self-managed environment.
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Home Based Labelling jobs near you
Associate Director, Medical Device Labeling and UDI # 4648

Associate Director, Medical Device Labeling and UDI # 4648

GRAIL

Durham, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago

Job description

Our mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care.

We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine's greatest challenges.

GRAIL is headquartered in the bay area of California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies.

For more information, please visit grail.com

The Associate Director, Quality Labeling Operations is responsible for establishing, implementing, maintaining, and continuously improving GRAIL's product labeling program. This role partners closely with Regulatory Affairs, Operations, Marketing, Supply Chain, R&D, Clinical Laboratory, Clinical Operations, and Design/Artwork to lead the global product labeling controls for GRAIL's regulated in vitro diagnostic (IVD) medical devices. This individual contributor role is the SME responsible for the development, implementation, and lifecycle management of compliant product labeling content, including Instructions for Use (IFU), Unique Device Identifier (UDI) labeling, and other product labeling elements required under FDA, EU IVDR/MDR, and U.K. MHRA regulations. The individual applies critical thinking and sound judgment to solve broad, complex problems and regularly communicates status, risks, and recommendations to management.
 
Primary responsibilities include providing expertise and oversight to ensure GRAIL's product labeling operations achieve and maintain compliance with the EU In Vitro Diagnostic Regulation (IVDR), ISO 13485:2016, ISO 14971:2019, 21 CFR 801, 21 CFR 820, 21 CFR 809, Unique Device Identifier (UDI) requirements and related in vitro diagnostic medical device regulations.  
 
This role is based at our Durham, North Carolina, office. It offers a flexible work arrangement, with the ability to work from GRAIL's office or from home. Our current flexible work arrangement policy requires that a minimum of 60%, or 24 hours, of your total work week be on-site. Your specific schedule, determined in collaboration with your manager, will align with team and business needs and could exceed the 60% requirement for the site.
 
Responsibilities:
  • Serve as the primary process owner for product labeling operations activities within the Quality Management System (QMS).Establish, maintain, and improve product labeling processes, procedures, and infrastructure (including electronic labeling systems, proofing, and physical and electronic distribution controls).
  • Establish and maintain labeling specifications and source artwork files (printed and electronic).
  • Ensure all product label claims are substantiated through the Design History File in partnership with Regulatory, Design Quality, and Research, Design, and Operations teams.
  • Partner with Marketing and Regulatory teams to align product labeling controls with advertising/promotional labeling controls, which are managed by the Promotional Material Review Committee and led by Marketing.
  • Initiate and support Veeva change control workflows for product labeling specifications which evaluate design history file (DHF) and risk management file (RMF) impacts.
  • Maintain inspection-ready product labeling documentation and traceability between product labeling, risk files, and technical documentation.
  • Ensure only current, approved product labels are distributed in print and electronically.
  • Drive cross-functional alignment and governance for labeling, ensuring Regulatory, Legal, and Clinical Study content oversight and compliant execution.
  • Manage label verification and validation, including proof review, barcode functionality, and compliance with UDI, GUDID, and GS1 requirements.
  • Provide direction to cross-functional teams on product labeling compliance requirements.
  • Align global core product labeling with regional requirements while supporting local adaptations for major markets.
  • Represent the Product Labeling Program as Subject Matter Expert during audits and inspections.
  • Monitor global regulatory changes and lead labeling process updates to maintain compliance that is aligned with our Commercial strategy.
 
Required Qualifications:
  • BS/BA degree & 10+ years of related experience, or Masters & 8+ years of related experience, or PhD & 5+ years of related experience.
  • Working knowledge of applicable medical device regulations and standards including but not limited to 21 CFR 801, 21 CFR 809, 21 CFR 820, ISO 13485:2016, ISO 14971:2019, MDR/IVDR.
  • Experience establishing and implementing medical device UDI, compliant with both FDA and EU regulations." 
  • Proven expertise remediating and improving a medical device labeling process to ensure an effective, compliant, inspection-ready program.
  • Experience using an eQMS required; Veeva Vault preferred.
  • Proven ability to efficiently manage workload under tight deadlines and pressure in a composed manner.
  • Demonstrated ability to perform meticulous work with a high degree of accuracy and completeness.
  • Experience supporting regulatory inspections/audits and responding to findings.
  • Expertise managing data reporting and communications using tools including Smartsheet, Confluence, Google Docs and Google Slides.
  • Proven leadership, organizational and management skills to drive effective, compliant cross-functional decision making.
  • Excellent written and verbal communication skills and attention to detail.
  • Ability to comprehend and interpret technical information related to GRAIL's product claims.
  • Experience preparing for, leading, and supporting FDA and EU Notified Body regulatory inspections/audits and effectively responding to findings.
Preferred Qualifications:
  • BS/BA degree & 12+ years of related experience
  • ASQ Certified Quality Auditor, Certified Quality Engineer, or similar preferred.
  • Experience working within a clinical laboratory (high complexity CLIA/CAP environment, compliant with ISO 15189) preferred.
  • Next Generation Sequencing (NGS) experience preferred.
Physical Demands and Work Environment
  • Work performed in office, production, and laboratory environments; frequent cross-functional engagement.
  • Travel may be required to support audits, inspections, or collaboration with global teams and suppliers.
  • Use of PPE in production and laboratory settings may be required.
  • Standard weekday schedule with flexibility for extended hours during regulatory inspections, customer visits, or critical investigations.
 
The expected, full-time, annual base pay scale for this position is $146,000 - $194,000 .  Actual base pay will consider skills, experience, and location.

This role may be eligible for other forms of compensation, including an annual bonus and/or incentives, subject to the terms of the applicable plans and Company discretion. This range reflects a good-faith estimate of the range that the Company reasonably expects to pay for the position upon hire; the actual compensation offered may vary depending on factors such as the candidate's qualifications. Employees in this role are also eligible for GRAIL's comprehensive and competitive benefits package, offered in accordance with our applicable plans and policies. This package currently includes flexible time-off or vacation; a 401(k) retirement plan with employer match; medical, dental, and vision coverage; and carefully selected mindfulness programs.

GRAIL is an equal employment opportunity employer, and we are committed to building a workplace where every individual can thrive, contribute, and grow. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, gender, gender identity, sexual orientation, age, disability, status as a protected veteran, , or any other class or characteristic protected by applicable federal, state, and local laws. Additionally, GRAIL will consider for employment qualified applicants with arrest and conviction records in a manner consistent with applicable law and provide reasonable accommodations to qualified individuals with disabilities. Please contact us at [email protected] if you require an accommodation to apply for an open position.

GRAIL maintains a drug-free workplace. We welcome job-seekers from all backgrounds to join us!
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