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Global Regulatory Affairs Associates - 1 Year Fixed Term Contract

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Research & Development
💼
United Kingdom
Thanks for your interest in the Global Regulatory Affairs Associates - 1 Year Fixed Term Contract position. Unfortunately this position has been closed but you can search our 591 open jobs by clicking here.

 

 

We currently have 2 fixed term contract  Regulatory opportunities of 1 year duration each.  One position is focused on NPD, strategies and registrations within the Health & Hygiene team. The other is within the Product Integrity Review team and is focused on ensuring Safety, Quality and Regulatory compliance throughout the product lifecycle.

 

 

The Associate will enable delivery of NPDs to global markets by providing key skills and expertise in dossier creation, working to support an integrated approach to regulatory planning across innovation and will provide SME knowledge into your assigned projects. You will ensure that all regulatory activities are completed according to the best process, in a consistent approach across projects.  

 

 

Key responsibilities will include:

  • Manage a complex and diverse set of registration/regulatory requirements across multiple markets and brands to enable the strategic delivery of a global pipeline.
  • Contribute to the development of regulatory strategies to enable successful registration in global markets with a focus on New Product Development
  • Maintain and develop knowledge and intelligence across the Regulatory Function to build ‘right first time’ approach with respect to registrations globally.
  • Collaborate with partner functions to agree market specific data requirements and delivery timelines
  • Develop excellent working relationships with local (regional) regulatory colleagues to facilitate aligned regulatory plans and shared learnings to ensure efficient speed to market.
  • Create strong and proactive relationships with all partner functions
  • Work collaboratively with Snr Manager/Manager in order to define and implement the regulatory strategy
  • Assist in monitoring, collecting, interpreting and sharing with business partners, regulatory issues and trends that will impact RB products, policies and procedures.  Assist in the development of strategies and plans of action to address them. 
  • Assist in the preparation of responses to address significant safety, regulatory and PR issues in the assigned Category  

 

 

 

Is this you?

 

  • Educated in a scientific field or equivalent experience. Honours degree is a plus.
  • Relevant Regulatory experience and knowledge in dossier / technical file creation and global registrations. Candidates with a Quality background will also be considered.
  • Experience in cosmetics regulations highly desirable, (additional regulations would be a plus e.g. medical devices) OR Biocides/disinfectants
  • Knowledge of the Regional and Global regulatory environment and how it impacts regulatory dossiers and registration.
  • Experience in preparing and submitting dossiers, variations and renewals. 
  • Understanding of global product development practice, rules, regulations and guidelines.
  • Familiarity with factors likely to influence the regulatory environment, including new and emerging guidelines relevant to dossier deliveries. 
  • Ability to consistently deliver to time, cost and quality standards in a fast-paced environment 
  • Ability to work on own initiative and be a self-starter
  • Excellent communication, influencing and stakeholder management skills

 

 

 

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