I am looking to speak with someone looking to kickstart their career in Pharmaceutical Manufacturing Regulatory Affairs with a top 5 global pharmaceutical organisation based in Berkshire, UK.
You will be responsible for providing regional regulatory expertise in supporting the delivery of high quality and efficient regulatory submissions, approvals, and local labelling for their assigned products
To be successful in this role you will have the following qualifications and experience
* Bachelor’s degree in scientific or health sciences discipline
* Industry-related or other relevant work experience in 1-3 years
* Knowledge of local/regional regulatory procedures and practices
* Knowledge of the drug development process
* Ability to find solutions and alternatives through teamwork embracing diversity, equity and inclusion resulting in positive business outcomes
* Ability to assess and propose ways to manage risk in a highly regulated environment
If this is of interest and you'd like to learn more, send your CV to jamie.keith@cpl.com