Regulatory Affairs Manager Theraflu/Otrivin

☞ Haleon

View: 131

Update day: 25-04-2024

Location: Nyon Vaud VD

Category: Arts / Design

Industry:

Job type: Temps plein, Temps de travail : 90-100%

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Job content

Job Description

Site Name: Switzerland - Nyon
Posted Date: Nov 15 2022


The purpose of this role is to provide regulatory support to assigned products/projects or parts of projects to enable our products to be successfully introduced or maintained Globally. In this role the individual is likely to support other members of the functional team but may also work in Project Teams and build trusting relationships with multi-functional teams within the sub-category and with the LOCs to ensure all regulatory requirements are met for both new innovation and existing products according to GSK Values.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Acts as a Business Partner and provides regulatory advice to a project on aspects of drug/cosmetic/devices/foods and supplements (dependent on category) development as appropriate.
  • Develops regulatory strategies under supervision working within Project Teams in order to secure competitive approvals and speed to market in conjunction with LOC regulatory teams.
  • Communicates effectively with the immediate functional team and within cross-functional Project Teams.
  • Delivery of high quality regulatory files to agreed timelines
  • Inputs to non-product related activities both within the function in order to direct new policy or pioneer new processes or improvements to GSK’s competitive advantage.
  • In conjunction with the category regulatory CMC lead, ensure support for the full life cycle of products, including: maintenance activities; Design to Value, complexity reduction, value engineering initiatives; change controls, etc. with supply chain and technical excellence Ensures compliance of their actions by adhering to global, regional and local processes, policies, SOPs and working instructions.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • BA or BSc in Life Science/ Pharmaceutically- related science
  • A first experience in regulatory affairs
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Deadline: 09-06-2024

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