Junior Regulatory Affairs Officer

• Location: Reading
• 12 month fixed term contract
  
  

About The Job

As a Junior Regulatory Affairs Officer you will obtain, manage and maintain product Marketing Authorisations for the UK and Ireland in line with business goals and legal requirements.

This role will see you conduct associated regulatory activities for the specified markets under the guidance and supervision of line management, and contribute to the implementation and leading of projects.

At Sanofi we chase the miracles of science to improve people’s lives. We are dedicated to making a positive impact on the lives of the patients and families we serve, and we accomplish our goals through world-class research and with the compassion and commitment of our employees.

Main Responsibilities

• Co-ordinate, prepare, submit and follow up registration applications to the UK and /or Irish regulatory authorities, expeditiously and to high standards, to ensure that marketing authorisations are obtained and maintained in line with the company's plans and goals. Support the launch of new products and life cycle management of the existing portfolio.
• Assist and provide support in the preparation, distribution and follow up of registration documentation required in the EU (particularly UK and Ireland).
• In order to achieve success, it is essential that the Junior Regulatory Officer under the guidance and supervision of line management:
• Ensures that all data supplied to the regulatory authorities are of the highest quality possible in terms of both content and presentation, whilst meeting agreed deadlines.Supports activities to obtain, manage and maintain product Marketing Authorisations in line with business goals and legal requirements. Conducts associated regulatory activities for the specified markets under the guidance and supervision of line management and contributes to the implementation and leading of projects. Provides regulatory input, with support, to commercial strategic and operating planning process.
  

About You

• Vaccine experience/knowledge mandatory.
• Experience in post-Brexit regulatory activities is highly desirable.
• Prior experience of managing regulatory packaging changes is desirable.
• Life sciences or chemistry degree or equivalent professional qualification.
  
  

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
• Join us in shaping the future of respiratory care and making a difference in the lives of patients across the NHS.
  
  

Visas for those who do not already have the right to work in the UK will be considered on a case by case basis according to business needs and resources.

We are proud to be a Disability Confident Employer, committed to offering interviews to candidates who request consideration under the Scheme and meet the minimum requirements for this role.

If you have a disability and require adjustments for the interview process, please email us at [email protected]. We are dedicated to ensuring an inclusive and supportive experience for all applicants.

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