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How much do global labeling jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for global 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 is global labeling?

Global labeling is a job role that involves developing, managing, and ensuring the accuracy of product labels and packaging information across multiple markets. It requires knowledge of regulatory requirements, attention to detail, and often the use of labeling software or databases to maintain consistency and compliance worldwide.

What jobs in the US pay 300,000 a year?

In the field of global labeling, senior roles such as Global Labeling Manager, Director, or Vice President can reach or exceed a $300,000 annual salary, especially with extensive experience, leadership responsibilities, and industry expertise. These positions often require advanced knowledge of regulatory compliance, project management, and cross-functional coordination, typically within large multinational companies. Compensation varies based on company size, location, and individual qualifications.

What is a Global Labeling job?

A Global Labeling job involves managing the development, updates, and compliance of product labeling for pharmaceutical, biotech, or medical device companies. Professionals in this role ensure that labeling documents, including package inserts and safety information, align with global regulatory requirements. They collaborate with cross-functional teams, including regulatory affairs, medical, and legal departments, to maintain accuracy and consistency. Global Labeling specialists also track regulatory changes and implement updates to ensure compliance in different markets.

What jobs pay 200,000 a year in the USA?

In the context of global labeling roles, senior positions such as labeling managers, regulatory affairs directors, or quality assurance executives can reach or exceed $200,000 annually, especially with extensive experience and certifications. High-level roles in related fields like project management or compliance within manufacturing or pharmaceutical industries may also offer salaries in this range.

What are the main responsibilities of a Global Labeling professional on a day-to-day basis?

On a typical day, a Global Labeling professional coordinates the development, review, and maintenance of product labeling to ensure compliance with varying international regulations. This often involves collaborating closely with cross-functional teams such as regulatory affairs, medical writing, marketing, and quality assurance to gather and validate product information. They also manage updates to labeling documents, monitor regulatory changes in target markets, and prepare submissions for regulatory agencies. The role requires balancing the accuracy and clarity of labeling content while managing multiple projects and tight deadlines.

What jobs pay $500,000 a year in the US?

In the field of global labeling, senior executive roles such as Vice President or Director of Global Labeling can reach or exceed $500,000 annually, especially in large multinational companies. These positions typically require extensive experience, leadership skills, and knowledge of regulatory compliance, often supplemented by advanced certifications or industry expertise.

What are the key skills and qualifications needed to thrive in the Global Labeling position, and why are they important?

To thrive as a Global Labeling professional, you typically need a background in life sciences, regulatory affairs, or pharmaceuticals, coupled with a thorough understanding of international labeling requirements and product regulations. Familiarity with regulatory databases, document management systems, and certifications such as RAC (Regulatory Affairs Certification) are highly beneficial. Exceptional attention to detail, strong organizational abilities, and clear cross-cultural communication skills set candidates apart in this role. These competencies are crucial for ensuring compliant and timely product labeling across global markets, reducing risks and supporting successful product launches.

More about Global Labeling jobs
What cities are hiring for Global Labeling jobs? Cities with the most Global Labeling job openings:
What are the most commonly searched types of Global Labeling jobs? The most popular types of Global Labeling jobs are:
What states have the most Global Labeling jobs? States with the most job openings for Global Labeling jobs include:
What job categories do people searching Global Labeling jobs look for? The top searched job categories for Global Labeling jobs are:
Global Labeling jobs near you
Infographic showing various Global Labeling job openings in the United States as of July 2026, with employment types broken down into 85% Full Time, 10% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $63,493 per year, or $30.5 per hour.
Principal Scientist, Global Labeling Regulatory

Principal Scientist, Global Labeling Regulatory

ImmunityBio

Summit, NJ • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Job description

Company Overview
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease.
Why ImmunityBio?
* ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
* Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
* Work with a collaborative team with the ability to work across different areas of the company.
* Ability to join a growing company with professional development opportunities.

Position Summary

The Principal Scientist, Global Labeling will report to the Director, Global Labeling and be responsible forthe strategic global development, maintenance, and compliance of product labeling throughout a drug's lifecycle. This expert will work with other cross-functional teams and SMEs to ensure that all labeling for investigational and marketed drugs meet the regulatory requirements of global health authorities.

Essential Functions

  • Create and execute global labeling strategies from early clinical development through commercialization.
  • Contribute to writing and maintaining key labeling documents, such as US Prescribing Information (USPI), and the EU Summary of Product Characteristics (SmPC).
  • Ensure that all labeling content and artwork comply with international and local Health Authority regulations (e.g., FDA, EMA, MHRA etc.) and Good Manufacturing Practices (GMP). This includes monitoring for regulatory changes and implementing updates.
  • Act as the primary labeling representative on various project teams, coordinating with departments like Clinical, Safety, Medical Affairs, Quality, Commercial, and Supply Chain.
  • Manage the process of updating label content and artwork for packaging and supplies, coordinating with manufacturing and third-party vendors.
  • Advise internal stakeholders on labeling content, processes, timelines, and potential risks, and present labeling strategies to senior leadership.
  • Lead or support negotiations with Regulatory Agencies regarding the content of product labels.
  • Create label technical specifications
  • Creation of labeling related change controls
  • Review and approve label proofs provided by internal and external labeling teams
  • Assist with the preparation of responses to Health Authority comments and questions pertaining to labeling issues.
  • Performs ad-hoc and cross-functional duties and/or projects assigned to support business needs and provide developmental opportunities.

Education & Experience

  • Bachelor's degree in life sciences or related field with 10+ years' experience working on clinical and commercial labels for varied types of drug products in a global setting required; or
  • Master's degree in life sciences or related field with 8+ years' experience working on clinical and commercial labels for varied types of drug products in a global setting required.
  • Familiar with organizing responses to Health Authority requests required
  • Experience with Veeva Vault preferred

Knowledge, Skills, & Abilities

  • Expert in Global Health Authority Regulatory labeling requirements for both clinical and/or commercial stage products
  • Proficient in Electronic Document Management Systems
  • Ability to work with firm deadlines and adapt quickly to changing requirements and priorities
  • Strong organizational skills, written and oral communication skills, and attention to detail.
  • Keen awareness of cultural sensitivities
  • Experience working in a complex and matrix environment
  • Excellent interpersonal skills

Working Environment / Physical Environment

  • This position works on site in Summit, NJ.
  • Regular work schedule is Monday-Friday, within standard business hours. Flexibility is available
  • A Principal Scientist may need to sit for long periods of time and use various computer programs.
  • This desk-based role involves the close study of scientific and regulatory documents.
  • They will work closely with scientific colleagues throughout the day, often on a project team basis.

This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.

$168,000 (entry-level qualifications) to $184,400 (highly experienced) annually

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options * Health and Financial Wellness Programs * Employer Assistance Program (EAP) * Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability * Healthcare and Dependent Care Flexible Spending Accounts * 401(k) Retirement Plan with Company Match * 529 Education Savings Program * Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks * Paid Time Off (PTO) includes: 11 Holidays * Exempt Employees are eligible for Unlimited PTO * Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day * We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.

At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

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