London, UK
Posted: Feb 07, 2025
HybridFull-time
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Job Description
Job Description

General Summary:

The Regulatory Labeling Senior Manager, Rest of World (ROW) is responsible for development and maintenance of product labelling for ROW markets across all therapeutic areas. This includes prescribing and patient information and associated business processes.

Key Duties And Responsibilities

  • Provides individual contribution in development, submission, negotiation and approval of ROW labelling.
  • Ensures compliance with labelling governance requirements and associated business processes.
  • Participates in label working groups and representing labelling at labelling governance meetings.
  • Works with Labelling Operations to ensure alignment with Package Component Labelling
  • Provides input into strategy for health authority interactions and advises stakeholders of regulatory labelling requirements regarding all aspects of labelling, including responses to questions, negotiations and inspections.

Knowledge And Skills

  • In-depth conceptual and practical knowledge regarding labelling requirements globally, use of CCDS or reference label (US and EU) in the development and management of local labelling.
  • Ability to develop, use, and apply knowledge of frameworks specific to regulatory regional labelling, and to use this information to support regulatory responsibilities that align with business objectives.
  • Ability to plan, prioritize, lead, and execute individual work, and teamwork related to regulatory global and/or regional labelling in a systematic and efficient manner.

Education And Experience

  • Bachelor’s degree
  • Extensive years of experience in regulatory affairs in the area of global labeling or related discipline, or the equivalent combination of education and experience

Flex Designation

Remote-Eligible

Flex Eligibility Status

In this Hybrid-Eligible role, you can choose to be designated as:

  • Hybrid: work remotely up to two days per week; or select
  • On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at
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Additional Info
Min. Experience
-
Job Location Type
Hybrid
Job Type
Full-time
Predicted Seniority Level
Mid-Senior level
Job Duration
-
Language(s)
All
Est. Budget/Pay Rate
To be discussed
Est. hrs
-
Optimal Job Start
-
Job Industry
Biotechnology Research, Pharmaceutical Manufacturing, and Research Services
Job Function
Legal
Employer
Vertex Pharmaceuticals
Preferred Applicant Countries
United Kingdom
Job Ref
J25E56E5AD34E
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