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Global Labeling Lead Remote Jobs (NOW HIRING)

As part of Global Labeling Strategy and Compliance (LSC), and under the supervision of the ... The Labeling Strategist, Sr. Manager will lead the development of the Core Labeling documents and ...

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$100K - $250K/yr

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Mountain View, CA ยท Remote

$100K - $250K/yr

Software Engineering Team Lead (Remote) Our client is at the forefront of crypto's cutting-edge ... By leveraging a global server network optimized for performance--and backed by investors such as ...

Technical Lead Remote (Web3)

Boston, MA ยท Remote

$100K - $250K/yr

Software Engineering Team Lead (Remote) Our client is at the forefront of crypto's cutting-edge ... By leveraging a global server network optimized for performance--and backed by investors such as ...

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Global Labeling Lead Remote information

See salary details

$30.5K

$105.9K

$141.5K

How much do global labeling lead remote jobs pay per year?

As of Jun 9, 2026, the average yearly pay for global labeling lead remote in the United States is $105,916.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $129,000.00 per year, depending on experience, location, and employer.

What is a Global Labeling Lead?

A Global Labeling Lead is a regulatory professional responsible for managing and coordinating the development, review, and maintenance of product labeling for pharmaceutical or medical device products across international markets. They ensure that all labeling materials comply with global regulatory requirements, including local adaptations and updates. This role involves collaborating with cross-functional teams, monitoring regulatory changes worldwide, and supporting product launches to ensure accurate and timely labeling. Working remotely, a Global Labeling Lead often uses digital platforms to communicate with global stakeholders and manage documentation.

What are the main challenges faced by a Global Labeling Lead working remotely, and how can they be addressed?

A Global Labeling Lead working remotely often faces challenges related to coordinating across multiple time zones, ensuring clear communication between cross-functional teams, and staying updated on evolving regulatory requirements in different markets. To address these challenges, it's important to establish strong digital communication routines, leverage collaborative project management tools, and proactively schedule regular check-ins with global stakeholders. Building good relationships with regulatory, clinical, and commercial teams also helps streamline the labeling review and approval process, ensuring labeling deliverables are accurate and timely.

What is the difference between Global Labeling Lead Remote vs Regulatory Labeling Specialist?

AspectGlobal Labeling Lead RemoteRegulatory Labeling Specialist
CredentialsTypically requires advanced degrees in life sciences or related fields, with experience in global labelingRequires similar degrees, often with specialized training in regulatory affairs
Work EnvironmentRemote, global coordination with cross-functional teamsPrimarily office or remote, focused on regulatory documentation
Industry UsageCommon in pharmaceutical and biotech companies managing global product labelingUsed across healthcare, pharmaceutical, and medical device sectors

The Global Labeling Lead Remote oversees global product labeling strategies, ensuring compliance across markets, often managing teams remotely. The Regulatory Labeling Specialist focuses on preparing and maintaining regulatory labeling documents, typically within a specific region or product. While both roles require regulatory knowledge and attention to detail, the Lead has broader responsibilities in global strategy and team coordination, whereas the Specialist concentrates on regulatory documentation and compliance at a more localized level.

What are the key skills and qualifications needed to thrive as a Global Labeling Lead, and why are they important?

To thrive as a Global Labeling Lead, you need a strong background in regulatory affairs, pharmaceutical labeling requirements, and project management, typically supported by a relevant science degree or equivalent experience. Familiarity with regulatory submission platforms, labeling management systems, and global health authority guidelines is critical. Excellent communication, cross-functional collaboration, and attention to detail are standout soft skills for this role. These competencies ensure accurate and compliant product labeling across markets, supporting product approvals and patient safety worldwide.
More about Global Labeling Lead Remote jobs
What cities are hiring for Global Labeling Lead Remote jobs? Cities with the most Global Labeling Lead Remote job openings:
What are the most commonly searched types of Global Labeling Lead jobs? The most popular types of Global Labeling Lead jobs are:
What states have the most Global Labeling Lead Remote jobs? States with the most job openings for Global Labeling Lead Remote jobs include:
Infographic showing various Global Labeling Lead Remote job openings in the United States as of June 2026, with employment types broken down into 82% Full Time, and 18% Contract. Highlights an 100% Remote job distribution, with an average salary of $105,916 per year, or $50.9 per hour.

Associate Director, Global Labeling Lead (remote)

BioNTech SE

Cambridge, MA โ€ข On-site, Remote

$146K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Job description

Cambridge, US; Gaithersburg, US; New Jersey, USย  ย |ย  ย full timeย  ย |ย  ย Job ID:ย 10671ย 

About the role:

You will be a member of the Global Labeling, Global Regulatory Affairs team and will lead all Labeling activities required for the development and maintenance of the Company Core Data Sheet, US prescribing and patient information and EU CP prescribing and patient information for BioNTech commercial products. In your role, you will act globally and work cross-functionally. At BioNTech, you will contribute to transforming the future of medicine while shaping a bestinclass Global Labeling function. You will work in an agile, sciencedriven environment with:

  • High strategic visibility in a global role at the interface of science, regulation and patient impact
  • Close collaboration with senior leaders and crossfunctional experts across the organization
  • The opportunity to build and refine global labeling standards, processes and systems in a rapidly evolving portfolio
  • A culture that values ownership, innovation, integrity and continuous learning

If you are passionate about advancing innovative therapies to patients worldwide and want to shape global labeling at scale, we look forward to receiving your application.

Your contribution:

  • Define and execute Labeling strategy for global life cycle management of medicinal products in BioNTech's responsibility for Primary Reference Labeling (i.e., the Company Core Data Sheet (CCDS), US Prescribing Information (USPI) and EU CP Summary of Product Characteristics [SmPC]). The strategy comprises management of local market label dependencies and country label differences when the local markets identify a need to review Primary Reference at the Labeling Team level
  • Build and lead cross-functional Labeling Teams
  • Responsible for timely preparation of Primary Reference labeling updates following update of the CCDS or on request of competent Health Authorities
  • Ensuring timely communication of updated CCDS content to local country offices for MAs in BioNTech's responsibility
  • Lead development and maintenance of regulatory processes and systems for Global Labeling
  • Identify critical Regulatory Labeling issues and proactively implement activities for their resolution including leading initiatives for Labeling within GRA or across functions at BioNTech
  • Act as the empowered delegate for the Head of Global Labeling as necessary

A good match:

  • Degree in pharmacy, chemistry, biology, biochemistry, medicine or equivalent
  • Advanced degree preferred, but not required
  • 9-16 years of professional working experience in Regulatory Affairs globally during development, registration and/or post-marketing for Biologics, Vaccines and/or Small Molecules, including direct experience in strategic Labeling content development and management and interacting with Health Authorities
  • Profound experience in leading the preparation and revision of product prescribing (and corresponding patient) information during registration and/or post-marketing, for CCDSs, EU CP SmPCs and USPIs
  • In depth knowledge of EMA and FDA regulatory requirements for product prescribing and patient information
  • Ability to work independently on very complex projects with minimal oversight
  • Excellent verbal and written communication skills in English

Your benefits and remuneration:

Expected Pay Range: $146,300,/year to 234,100/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.

BioNTech US is committed to employee wellbeing and offers best-in-class benefits & HR programs to support an inclusive & diverse workforce. Salaried/Position-Targeted Hourly Employees working 30+ hours per week are eligible for our comprehensive benefits package. Benefits include but are not limited to:

  • Medical, Dental and Vision Insurance
  • Life, AD&D, Critical Illness Insurance
  • Pre-tax HSA & FSA, DCRA Spending Accounts
  • Employee Assistance & Concierge Program (EAP) available 24/7
  • Parental and Childbirth Leave & Family Planning Assistance
  • Sitterstream: Virtual Tutoring & Childcare Membership
  • Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.
  • 401(K) Plan with Company Match
  • Tuition Reimbursement & Student Loan Assistance Programs
  • Wellbeing Incentive Platforms & Incentives
  • Professional Development Programs
  • Commuting Allowance and subsidized parking
  • Discounted Home, Auto & Pet Insurance

...and more! More details to be shared.

Apply now - We look forward to your application!

Apply for our Cambridge, US; Gaithersburg, US; New Jersey, USย location and simply send us your documents using our online form.

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.