Regulatory Affairs Specialist

3 days ago

Southampton, Southampton, United Kingdom Austin Vita Full time

This is a fantastic opportunity for a skilled professional to join Austin Vita as a Compliance Consultant. The position offers a unique blend of regulatory expertise and business acumen, with a focus on supporting change management activities and collaborating with cross-functional teams.


Key Responsibilities

As a Compliance Consultant, you will be involved in:

  • Supporting the development and implementation of regulatory strategies to ensure compliance with applicable regulations
  • Collaborating with Quality, R&D, and Manufacturing teams to manage sustaining changes across the medical device portfolio
  • Representing Regulatory Affairs in change boards and ensuring the appropriate regulatory action is taken during implementation
  • Working with global counterparts to assess the potential impact of planned changes and communicating implemented changes

Requirements

To be successful in this role, you will need:

  • Experience in Medical Device Regulatory Affairs
  • A university degree in a scientific subject
  • Excellent communication and organizational skills
  • Ability to work with cross-functional teams and diverse cultures

What We Offer

Austin Vita offers a dynamic and supportive work environment, with opportunities for professional growth and development. We are committed to attracting and retaining top talent, and offer a competitive compensation package and benefits.

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