Sr. Scientist-Global Labeling Lead

Merck; North Wales (Montgomery County); Hybrid; USD 106,000 - 167,000; Full time

Benefits offered by this job

Medical, dental, vision insurance (for

401(k) retirement plan

Paid holidays and vacation

Sick days

Job summary

Merck & Co., Inc. in Rahway, NJ seeks a Senior Scientist, Global Labeling Lead to develop and maintain Core Labeling and US/EU labeling for developmental and marketed products, supporting country regulatory labeling.

You will lead cross-functional labeling teams, ensure regulatory compliance, and guide labeling strategy and language to meet global standards while managing multiple priorities in a dynamic environment. Travel up to 10% with a hybrid work arrangement.

Qualifications

• Minimum of 3 years of labeling experience or other relevant pharmaceutical industry experience.
• Experience leading cross-functional labeling teams and communicating with senior management.
• Ability to assimilate complex clinical and scientific information and labeling precedents.

Responsibilities

• Develop, maintain, and implement Core Labeling for assigned products in line with internal standards and guidelines.
• Develop, maintain, and implement US Labeling for assigned products in line with regulatory requirements and internal standards and guidelines.
• Assist with developing and maintaining Local Labeling (EU and most of world) for assigned products.
• Provide labeling expertise and guidance to teams while ensuring compliance with applicable regulatory requirements.
• Serve as regulatory labeling point of contact on global Regulatory Affairs sub-teams to ensure delivery of labeling documents meeting quality and regulatory standards for submissions.
• Lead cross-functional teams to develop, review and approve Core and Local Labeling documents.
• Recommend strategies and labeling language for Core or Local Labeling during development or responses to Health Authority.

Skills

Labeling strategy

Regulatory affairs

Cross-functional leadership

Project management

Scientific knowledge

Technical writing

Regulatory submissions

Communication

Detail-oriented

Negotiation

Policy implementation

Time prioritization

Education

Bachelor's degree in a scientific or medically related discipline

Advanced degree (M.S., Pharm.D., or Ph.D.) preferred

Job description

Job Description

We invite you to join our mission of advancing the prevention and treatment of diseases. The purpose of Global Labeling is to drive labeling strategy and ensure high-quality and compliant labeling documents which, provide the safe and effective use of products for patients and healthcare providers globally.

We invite you to join our mission of advancing the prevention and treatment of diseases. The purpose of Global Labeling is to drive labeling strategy and ensure high-quality and compliant labeling documents which, provide the safe and effective use of products for patients and healthcare providers globally.

As part of Labeling Strategy function in Global Labeling, you will be accountable for developing labeling content and maintaining the target product labeling for developmental products, Core Labeling documents (e.g., CCDS, CCPPI, CCIFU), US Labeling, and EU Labeling for marketed products; and supporting country Regulatory Affairs in the development and maintenance of other country’s Local Labeling.

The Senior Scientist, Global Labeling Lead Is Responsible For

• developing, maintaining, and implementing Core Labeling for assigned products in line with internal standards and guidelines
• developing, maintaining, and implementing US Labeling for assigned products in line with regulatory requirements and internal standards and guidelines
• assisting with developing and maintaining Local Labeling (EU and most of world) for assigned products
• providing labeling expertise and guidance to teams while ensuring compliance with applicable regulatory requirements
• serving as regulatory labeling point of contact on global Regulatory Affairs sub-teams to ensure delivery of labeling documents that meet quality and compliance standards and regulatory labeling requirements to support timely regulatory submissions for assigned products
• leading cross-functional teams to develop, review and approve Core and Local Labeling documents
• recommending strategies and labeling language for inclusion in Core or Local Labeling during labeling development or responses to Health Authority

Education

• Bachelor's degree in a scientific or medically related discipline required; advanced degree (M.S., Pharm.D., or Ph.D.) preferred.

Required Experience & Skills

• Minimum of 3 years of labeling experience or other relevant pharmaceutical industry experience (e.g., Medical Affairs, Regulatory Affairs, Clinical, or Pharmacovigilance). An advanced degree with relevant labeling or pharmaceutical industry experience gained during graduate studies may be considered equivalent to the experience requirement.
• Experience leading cross-functional labeling teams, including interactions with senior management, strongly preferred. Demonstrated ability to actively listen, address labeling issues, develop action plans, build consensus, and drive projects to completion.
• Ability to assimilate complex clinical and scientific information, labeling precedents, and competitor labeling, and communicate findings clearly and concisely.
• Understanding of medical concepts and terminology.
• Project management skills with the ability to manage multiple priorities and meet deadlines.
• Proactive problem‑solving skills with the ability to make sound recommendations and decisions.
• Ability to work effectively in ambiguous environments and maintain an action‑oriented approach.
• Strong written and verbal communication skills.
• High attention to detail and commitment to accuracy.
• Demonstrated ability to influence, negotiate, and collaborate across functions.

Required Skills

Action-Oriented, Adaptability, Adverse Event Report, Communication, Detail-Oriented, Labeling Compliance, Negotiation, Pharmaceutical Product Development, Policy Implementation, Problem Solving, Regulatory Strategy Development, Regulatory Submissions, Scientific Knowledge, Technical Writing, Time Prioritization

US And Puerto Rico Residents Only

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.

Requirements

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

The salary range for this role is

$106,200.00 - $167,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

San Francisco Residents Only:

We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:

We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status

Regular

Relocation:

No relocation

VISA Sponsorship

No

Travel Requirements

10%

Flexible Work Arrangements

Hybrid

Shift

Not Indicated

Valid Driving License

No

Hazardous Material(s)

n/a

Job Posting End Date

09/26/2026

• A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.