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We would like to invite applications for the role ofRegulatory Affairs Associateat our Harlow office to supportEuropean Genericnew submissions via decentralised and mutual recognition procedures, typically for solid oral dosage forms, solutions and/or suspensions.
On a daily basis, with support from your line manager, you will be working cross-functionally with R&D colleagues to:
Through training and on the job experience you will develop and grow your understanding of the European regulatory environment and supporting data requirements.
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Dir Regulatory Affairs
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