Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Sr. Scientist-Global Labeling Lead

$106.2k - $167.2k

Merck & Co.

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. 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. Please click here if you need an accommodation during the application or hiring process. 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. Requisition ID: R416023 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. Learn more about your rights, including under California, Colorado and other US State Acts 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 . 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 #J-18808-Ljbffr Merck & Co.

Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the Sr. Scientist-Global Labeling Lead in North Wales, PA vacancy
  • Merck & Co., Inc. in Rahway, NJ, is seeking a Senior Scientist, Global Labeling Lead to develop, maintain, and implement Core Labeling and US Labeling for assigned products, and support Local Labeling for worldwide markets. You will lead cross-functional labeling teams,... 
    Senior
    Local area
    Worldwide

    Merck & Co.

    North Wales, PA
    1 day ago
  • $173k

     ...United States of AmericaJob Description:Sr. Distinguished Scientist - PSTS Neuroscience Disease Area...  ...Scientist - PSTS Neuroscience Disease Area Lead. Location options: Spring House,...  ...organizations (e.g. Regulatory affairs, Global Medical Safety, Clinical Pharmacology)... 
    Senior
    Full time
    Temporary work
    Local area

    Johnson & Johnson

    Spring House, PA
    4 days ago
  • Senior Scientific Leader as PSTS Neuroscience Disease Area Lead responsible for shaping and integrating disease-specific scientific strategy across discovery through registration phases within Johnson & Johnson. Responsibilities oversee scientific planning, risk management... 
    Senior

    Scorpion Therapeutics

    Spring House, PA
    1 day ago
  •  ...Johnson & Johnson's Innovative Medicine R&D seeks an Associate Director, Global Labeling Product Leader to develop and execute global labeling strategies for pharmaceutical products. You will lead target labeling development and collaborate across clinical, safety, regulatory... 
    Suggested
    Local area

    Jobleads-US

    Spring House, PA
    2 days ago
  •  ...Johnson & Johnson's Innovative Medicine R&D seeks an Associate Director, Global Labeling Product Leader to lead global labeling strategy and development for assigned products. This role operates within a complex, cross-functional environment and interfaces with regulatory... 
    Suggested
    Worldwide

    Jobleads-US

    Horsham, PA
    2 days ago
  •  ...An innovative firm is seeking an Associate Principal Scientist specializing in Clinical Outcome Assessment. This pivotal role involves coordinating global strategies for Patient-Reported Outcomes and ensuring alignment with regulatory requirements. You will collaborate... 
    Senior

    The Fountain Group

    Lansdale, PA
    3 days ago
  • $96.68k - $120.85k

     ...Ramboll is a global architecture, engineering, and consultancy company. As a foundation...  ...this position, the selected candidate will lead and support multidisciplinary teams working...  ...to early-career and mid-level Geological Scientists and contribute to the development of team... 
    Senior
    Full time
    Work at office

    Ramboll

    Blue Bell, PA
    2 days ago
  •  ...& Johnson's Innovative Medicine division is seeking a Senior Regulatory Affairs Professional to shape regulatory strategies and lead global submissions across multiple programs. You will partner with cross-functional teams to ensure compliant development and lifecycle... 
    Senior

    Scorpion Therapeutics

    Spring House, PA
    2 days ago
  •  ...in Spring House, PA, is seeking a Senior Laboratory Automation Scientist to own automation readiness for integrated workcells in discovery...  ...and biochemical workflows into executable automated sequences, lead design, integration, qualification, and lifecycle support, and... 
    Senior

    Johnson & Johnson

    Spring House, PA
    5 days ago
  •  ...US to support late-stage clinical development projects. You will lead programming tasks, develop analysis datasets, and deliver tables...  ...regulatory submissions. Responsibilities include coordinating a global programming team, ensuring quality and timeliness, and... 
    Senior

    Merck & Co.

    North Wales, PA
    1 day ago
  • $117k - $201.25k

     ...searching for the best talent for a Manager Global Regulatory Scientist, Regulatory Affairs. This hybrid work...  ...be responsible for organizing and leading meetings. Provide regulatory input...  ...views of HAs, regulatory precedents, labeling differences, and disease area-... 
    Local area
    Immediate start
    Flexible hours

    Johnson & Johnson Innovative Medicine

    Spring House, PA
    1 day ago
  • $190.8k - $300.3k

     ...and regulatory submissions that support global clinical development, product registration...  ...Preclinical Leaders, Compound Leaders, and scientists across NDS and/or Preclinical Development...  ...industry collaborations, and proactively lead internal cross-departmental initiatives... 
    Senior
    Full time
    For contractors
    Second job
    Local area
    Flexible hours

    Merck Sharp & Dohme (MSD)

    West Point, PA
    7 days ago
  •  ...Leader to guide safety strategy from discovery to development. You will lead safety science teams, develop risk assessments, analyze toxicology studies, and draft regulatory safety documents with global partners. The role emphasizes cross-functional collaboration,... 
    Senior

    Scorpion Therapeutics

    Spring House, PA
    2 days ago
  • Role Senior Scientist Product Lead CMC RA - Synthetics, New Modalities, focusing on global CMC regulatory strategies for innovative medicines. Responsibilities Develop and implement regulatory dossiers and strategies for development compounds Support global filings Prepare... 
    Senior

    Scorpion Therapeutics

    Spring House, PA
    2 days ago
  • Johnson & Johnson Innovative Medicine is recruiting a Distinguished Scientist, Nonclinical Safety Leader for Preclinical Sciences and...  ...can be located in Spring House, PA or Cambridge, MA. You will lead nonclinical safety strategy across portfolios and mentor PSTS teams... 
    Senior

    Johnson & Johnson Innovative Medicine

    Spring House, PA
    2 days ago
  •  ...Behring in King of Prussia, PA, seeks a Principal Medical Writer to lead medical writing strategy for one or more clinical Programs,...  ...regulatory submissions. This role partners with cross-functional teams globally, contributes to clinical development plans, and communicates... 
    Senior

    CSL Plasma Inc.

    King of Prussia, PA
    4 days ago
  • Johnson & Johnson's Innovative Medicine division is seeking a Senior Scientist, Biostatistics to design and analyze clinical studies,...  ...based decisions across development programs. The role requires leading projects, applying advanced statistical methods, including data... 
    Senior

    Scorpion Therapeutics

    Spring House, PA
    1 day ago
  • Johnson & Johnson Innovative Medicine seeks a Manager Global Regulatory Scientist to lead regulatory submissions and strategy in a hybrid, multi-country setup (Beerse, Leiden, High Wycombe, Raritan, Spring House). You will coordinate IND/CTA/MAA/NDA filings, manage timelines... 

    Johnson & Johnson Innovative Medicine

    Spring House, PA
    1 day ago
  • $107.6k - $161.5k

     ...We are seeking a passionate and experienced Senior Scientist/Team Leader - Bioprocess Development to lead downstream process development team focused on the chromatographic...  .... Partner with leaders across Ecolab’s global Bioprocessing labs to address complex purification challenges... 
    Senior
    Hourly pay
    Minimum wage
    Local area

    Ecolab

    King of Prussia, PA
    3 days ago
  •  ...a CBRE Facilities AuditReadiness Program Lead (or **Audit Readiness & Facilities ComplianceLead...  ...storage, mechanical areaconditions, labeling, organization, safety, compliance, and...  ...Whenyou join CBRE, you become part of a global leader in commercial real estate andinvestment... 
    Senior
    For contractors
    For subcontractor
    Work at office

    CBRE

    King of Prussia, PA
    4 days ago
  •  ...CBRE Facilities Audit Readiness Program Lead (or **Audit Readiness & Facilities Compliance...  ...storage, mechanical area conditions, labeling, organization, safety, compliance, and general...  ...When you join CBRE, you become part of a global leader in commercial real estate and... 
    Senior
    For contractors
    For subcontractor
    Work at office
    Visa sponsorship
    Monday to Friday

    CBRE Group, Inc.

    King of Prussia, PA
    3 days ago
  • $164k - $282.9k

     ...Innovative Medicine R&D is recruiting for a Distinguished Scientist, Nonclinical Safety Leader within Preclinical...  ...bring these molecules to humans and ultimately through global registration.Principal Responsibilities:Lead PSTS project teams of nonclinical safety and... 
    Full time
    Local area
    Immediate start

    Johnson & Johnson

    Spring House, PA
    14 days ago
  • Scorpion Therapeutics is seeking a Global Associate Director of Medical Affairs (GADMA) to support execution of the Global Medical & Scientific Affairs plans for assigned therapeutic areas with a US focus and ROW support. The role requires an MD/PhD/PharmD, 2+ years in... 

    Scorpion Therapeutics

    North Wales, PA
    3 days ago
  • Merck & Co. is seeking a Global Associate Director Medical Affairs (GADMA) to oversee scientific work and execution for assigned therapeutic areas with a primary focus on the US while supporting ROW. The role integrates with global teams to execute medical tactics, engage... 

    Merck & Co.

    North Wales, PA
    3 days ago
  • Merck in the United States seeks an Associate Director Publication Manager to lead global publication teams, drive strategy, and ensure policy compliance. You will coordinate with R&D, Human Health, and medical communications agencies to allocate resources for writing,... 

    Socket.dev

    North Wales, PA
    2 days ago
  • Scorpion Therapeutics seeks an Associate Director of Enterprise Brand Strategy within the Global Respiratory Business Unit. You will shape HCP engagement strategies and scientific narratives for respiratory therapies, driving global messaging across markets and internal... 

    Scorpion Therapeutics

    North Wales, PA
    2 days ago
  • Merck is seeking a Global Quality Program Integration Manager in West Point, PA to lead critical laboratory transformation initiatives within a fast-paced, matrixed environment. You will collaborate with stakeholders across regions and external partners to align programs... 

    Merck

    West Point, PA
    4 days ago
  • Merck is seeking an Associate Director Publication Manager to lead global publication strategy and tactical plans across assigned products. You will oversee Publication Teams, coordinate with internal writers and medical communication agencies, and drive development of... 

    MSD Malaysia

    North Wales, PA
    4 days ago
  • Merck & Co. is seeking an Associate Director Publication Manager to lead global publication strategies and tactical plans for assigned products. You will oversee Publication Teams, coordinate data dissemination, and ensure compliance with industry standards and policies... 

    Merck & Co.

    North Wales, PA
    2 days ago
  • Merck & Co. is seeking an Associate Director, Enterprise Brand Strategy to shape global HCP strategy, scientific narrative, and core commercial platforms for differentiated engagement across markets. You will partner with cross-functional teams to translate evidence and... 
    Local area

    Merck & Co.

    North Wales, PA
    4 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Sr. Scientist-Global Labeling Lead. Be the first to apply!