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Regulatory Labeling Associate Director Jobs (NOW HIRING)

IQVIA Holdings

Director, Labeling Strategy

Durham, NC · On-site

$128K - $358K/yr

Director Of Regulatory Labeling Strategy IQVIA is seeking a Director of Regulatory Labeling Strategy to support new programs to be based in the US. This role is intended for a forward looking ...

Posted today

IQVIA

Director, Labeling Strategy

Durham, NC · On-site

$128K - $358K/yr

IQVIA is seeking a Director of Regulatory Labeling Strategy to support new programs to be based in the US. This role is intended for a forward looking, creative regulatory professional able to ...

IQVIA, Inc.

Director, Labeling Strategy

Durham, NC · On-site

$128K - $358K/yr

IQVIA is seeking a Director of Regulatory Labeling Strategy to support new programs to be based in the US. This role is intended for a forward looking, creative regulatory professional able to ...

Eisai, Inc.

Director, Global Labeling

$188K - $247K/yr

... global regulatory labeling strategies to support business objectives and patient needs. The ... direct product responsibilities and will also be providing oversight to a high-performing team of ...

IQVIA

Director, Labeling Strategy

Durham, NC · On-site

$128K - $358K/yr

IQVIA is seeking a Director of Regulatory Labeling Strategy to support new programs to be based in the US. This role is intended for a forward looking, creative regulatory professional able to ...

Eisai

Director, Global Labeling

$188K - $247K/yr

... global regulatory labeling strategies to support business objectives and patient needs. The ... direct product responsibilities and will also be providing oversight to a high-performing team of ...

ImmunityBio

Director, Global Labeling Regulatory

Summit, NJ · On-site

$159K - $210K/yr

Position Summary The Director, Global Labeling Regulatory will orchestrate the strategic global development, maintenance, and compliance of product labeling throughout a drug's lifecycle. This ...

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Regulatory Labeling Associate Director information

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How much do regulatory labeling associate director jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for regulatory labeling associate director 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 does a regulatory labeling associate director do?

A Regulatory Labeling Associate Director is responsible for overseeing the creation, review, and maintenance of product labeling for pharmaceuticals, biologics, or medical devices to ensure compliance with global regulatory requirements. They collaborate with cross-functional teams, including regulatory affairs, clinical, and legal departments, to develop labeling that accurately reflects product safety and efficacy. This role also involves staying updated on regulatory changes, guiding labeling strategy, and interacting with health authorities during product submissions and approvals. Their work helps ensure that product information provided to healthcare professionals and patients is clear, accurate, and meets all legal standards.

What are the key skills and qualifications needed to thrive as a regulatory labeling associate director?

To thrive as a Regulatory Labeling Associate Director, you need deep expertise in regulatory affairs, drug labeling requirements, and global health authority guidelines, typically supported by a degree in life sciences or pharmacy. Proficiency with regulatory submission tools, document management systems, and familiarity with eCTD and labeling software is crucial. Exceptional attention to detail, leadership, and strong cross-functional communication skills distinguish top performers in this role. These skills ensure accurate, compliant product labeling and successful coordination with internal teams and regulatory agencies, which are vital for product approval and patient safety.

What are some common challenges faced by a regulatory labeling associate director when managing global product labeling across different regions?

A Regulatory Labeling Associate Director often encounters challenges such as navigating varying and frequently changing regulatory requirements across multiple countries, synchronizing updates to ensure global consistency, and coordinating cross-functional teams including regulatory, medical, and legal departments. Balancing tight timelines for product launches or updates while ensuring accuracy and compliance is also a key challenge. Effective communication and proactive planning are essential to address these complexities and maintain alignment with both internal stakeholders and health authorities.

What are popular job titles related to Regulatory Labeling Associate Director jobs?

For Regulatory Labeling Associate Director jobs, the most frequently searched job titles are:

Infographic showing various Regulatory Labeling Associate Director job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $63,493 per year, or $30.5 per hour.

Regulatory Labeling Lead (On-site)

Princeton, NJ • On-site

Abbott
See more jobs at Abbottexternal

Full-time

Medical, Life, Retirement

Re-posted 11 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 139 frontline employees who took The Breakroom Quiz

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:

Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

  • Career development with an international company where you can grow the career you dream of.

  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

  • An excellent retirement savings plan with a high employer contribution.

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.

  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
This position works out of our Princeton, NJ location in the Abbott Point of Care (APOC), Diagnostics Division. We're empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott's diagnostics instruments, providing lab results for millions of people.

The Regulatory Labeling Lead will serve as the subject matter expert for regulatory labeling strategy across the i-STAT global IVD product portfolio. You will provide strategic guidance on labeling content, regulatory interpretation, and governance while partnering with Regulatory Affairs, Quality, Operations, R&D, Marketing, and global stakeholders to ensure product labeling remains compliant, consistent, and effective throughout the product lifecycle. This is a highly visible individual contributor role that combines regulatory expertise, cross-functional leadership, and strategic influence. You will lead initiatives that shape labeling processes and standards while supporting global regulatory compliance, UDI implementation, and labeling innovation.

What You'll Work On

Regulatory Labeling Strategy

  • Develop and maintain regulatory labeling strategies for i-STAT IVD products throughout the product lifecycle.

  • Interpret global labeling regulations and standards and translate requirements into practical, compliant labeling solutions.

  • Provide strategic guidance on labeling content, claims, warnings, precautions, symbols, instructions, and intended use language.

  • Evaluate complex and ambiguous labeling challenges and recommend risk-based approaches.

Labeling Governance & Compliance

  • Establish and maintain labeling standards, procedures, and best practices.

  • Drive consistency across labels, instructions for use, user documentation, packaging, and related product information.

  • Ensure labeling decisions are appropriately documented and inspection ready.

  • Support continuous improvement of labeling processes and controls.

UDI & Global Initiatives

  • Lead global UDI strategy, implementation, and ongoing compliance activities.

  • Support initiatives involving digital labeling, global harmonization, and labeling process transformation.

  • Monitor evolving global labeling requirements and assess impact to business processes and products.

Cross-Functional Leadership

  • Serve as recognized expert on regulatory labeling matters.

  • Lead cross-functional discussions to align stakeholders on labeling strategies and content decisions.

  • Influence decisions through technical expertise and regulatory knowledge.

  • Mentor colleagues and help strengthen organizational labeling capabilities.

Required Qualifications

  • Bachelor's degree in Life Sciences, Clinical Laboratory Science, Engineering, Regulatory Affairs, Technical Communications, or a related field, or an equivalent combination of education and experience.

  • Typically, 8+ years of experience in Regulatory Affairs, medical device or IVD labeling, quality systems, product development, or other regulated environments.

  • Experience interpreting global medical device and/or IVD labeling requirements.

  • Experience leading cross-functional initiatives in a matrixed organization.

  • Strong communication, collaboration, and stakeholder management skills.

  • Demonstrated ability to influence decisions without direct authority.

Preferred Qualifications

  • Experience supporting global IVD products and international regulatory requirements.

  • Experience with UDI compliance, implementation, and lifecycle management.

  • Experience supporting regulatory inspections, audits, or external assessments.

  • Experience developing global labeling strategies and governance processes.

  • RAC, ASQ, or other relevant regulatory or quality certifications.

  • Experience with digital labeling, IVDR, MDR, or global labeling harmonization initiatives.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.

The base pay for this position is

$99,300.00 - $198,700.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Regulatory OperationsDIVISION:APOC Point of CareLOCATION:United States > Princeton : 400 College Road EastADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 5 % of the TimeMEDICAL SURVEILLANCE:Not ApplicableSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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