Labelling Hub Manager New

apartmentCPL placeDublin calendar_month 

On behalf of our client, a global pharmaceutical company, we are currently recruiting for a Labelling Hub Manager (Regulatory). This is a permanent, full-time role. This is a hybrid role with approx 3 days a week in the North Dublin office.

Role

The Labelling Hub manager is responsible for regulatory activities pertaining to labelling updates for determined country/ies according to internal procedure and legislation applied to country/ies under her/his responsibility.

Provide Subject Matter Expert support to the Global Labelling Hub and Global Compliance Director, and other Stakeholders, with initiatives which impact, or may impact, labelling activities within the determined region and country/ies.

Every day, we rise to the challenge to make a difference and here’s how the Labelling Hub Manager role will make an impact:

  • Point of Contact to Global Labelling Team regarding countries/licenses under her/his responsibility
  • Reports on agreed key performance indicators for set region.
  • Onboards and manages regional assigned labelling associates.
  • Communicate clearly issues and resolutions to peers and subordinates in a meaningful way.
  • Ensure local labelling text is prepared right first time and on-time according to agreed company procedures and objectives.
  • Support regional labelling team members with health authority questions, requests for further information, preparation, and review of labelling documents prior to submission.
  • Advise Global Labelling Hub and Global Compliance Director regarding any deficiencies or issues.
  • Ensure that supportive documents, not limited to Core Data Sheet or other Reference Label such as USPI, SmPC, are obtained in a timely manner to the countries according to local legislation
  • Arranges and updates Local Labelling texts above market on behalf of all impacted markets to ensure their conformity with internal procedures and local legislation.
  • Manage all labelling variations through the Regulatory Information Management System and Trackwise Change control environment as needed to show compliance with global submission timelines and a valid reason for delay.
  • Liaise with Translation vendors as needed.
  • General knowledge of preparing artwork from labelling text and the interface with Launch Management, Supply Chain and Quality teams.
  • Ensures maintenance of relevant systems according to relevant SOPs.

Requirements:

  • Bachelor’s degree in science, Medicine or Pharmacy, or another related field. Advance degree is a plus (
  • Labelling and Regulatory experience
  • Regulatory experience working with Regional Health Authorities and in-depth Regional Labelling knowledge
  • Highly developed interpersonal, presentation and communication skills with advanced local language capability
  • Ability to provide innovative approaches/recommendations to product labelling that meet corporate goals while maintaining compliance with relevant laws and regulations.
  • Understand GLC requirements/ processes and EU/ US regulatory requirements.
  • The ability to influence effectively in a matrixed, cross-functional team environment

For a full Job Spec and to apply for this role please call Linda on 01 2784703 or e-mail [email protected]

Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671

#LI-LD1

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