Title: Senior Regulatory Affairs
I am currently looking for a Senior Reg Affairs (RA) specialist, you’ll be working with one of the UK largest manufactures of generic pharmaceutical and over the counter (OOC) medicines. They will be offering you the chance to build on your regulatory exposure, giving you the chance to work on global portfolios. They have an abundance of employee benefits and perks such as a generous pension scheme and holiday allowance, oh and there is always on-going professional development.
You a Senior RA Executive will be a key member of the team, supporting NPD and existing licence maintenance, proposing improvements to internal systems, representing the department at internal and external meetings and providing advice on regulatory requirements. You’ll prepare, submit and manage new market authorisation applications, variations and renewals to various markets around the world.
This is a perfect position for someone who is seeking their next step up within Regulatory affairs, you will have, had previous experience of European Regulatory Affairs particularly in CMC. You’ll be comfortable handling new marketing authorisation applications and post-licensing activities. You’ll be a “Go-getter”, self-motivated individual with a strong eye to detail.
If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to email@example.com. For more information regarding this position or any others, please call Dan on 0161 868 2205.
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Keywords: RA, Reg Affairs, Regulatory, CMC, Regulatory Affairs, GMP.