Your new company
This a flagship business within the NHS which manufactures and distributes terminally sterilised injectables for the secondary care market in the UK and worldwide. They Opened a new manufacturing site in 2017 supported by a £26m investment. They aim to double the size of the business in the next 4-5 years. This is a semi-autonomous business unit and has its own Management Board. Due to projects and expansion. They are looking for Regulatory Affairs Specialist.
Your new role
This is an exciting flagship business to work, with a fast pace environment. Responsible for the generation & submission of regulatory documentation to regulatory agencies. Maintain Marketing Authorisations in line with the commercial strategy to support the current & future business targets. Responsible for maintaining the post market product regulatory lifecycle. There office is in Torbay in the UK. The team works closely together and creates a supportive, flexible, happy environment that is committed to delivering quality outcomes against targets.
What you'll need to succeed Degree in relevant subject area or equivalent experience
2 years+ experience of working within the pharmaceutical industry
What you'll get in return
Flexible working options available. Competitive Market Salary and Fully remote role with 1 day a month attendance required in the office.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
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Tipo de empleo
Hablar con un consultor
Hablar con George Costard, El consultor especializado que lleva esta posición, ubicado en London-City