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Regulatory Executive - CMC
Office based - Middlesex
i3 are currently recruiting for a Regulatory Affairs Executive with extensive experience of CMC regulatory submissions and documents for a new contract position. This opportunity is working within an established Regulatory department of a world leading Pharmaceutical company based in Middlesex.
In this position you will primarily be responsible for the preparation of Chemistry Manufacturing and Control (CMC) documents using a variety of information sources and liaising closely with other colleagues/groups to ensure the high quality of the document. You will be required to ensure project needs are met and agreed deadlines are adhered to, highlighting potential delays. This position is working at a strategic level liaising with relevant business partners and is not a submissions role.
This is a 6 months contract assignment initially which would suit someone experienced in Regulatory Affairs, with specific and detailed CMC experience essential. Candidates should have a strong interpersonal and communication skills as well the ability to work independently. You must possess full eligibility to work in the UK.
This is a full time role based at the client's offices.
Offered via i3 Pharma Resourcing through either full employment (salary & benefits) or as a freelance contract.
Please apply or telephone 01895 451 809
Key Words: Regulatory Affairs, Medicines Control Agency, MCA, Post-approval regulatory affairs, CMC, Clinical Regulatory, Full Time, Contract, Permanent, CRO, Submissions, Variations, Labelling, PILs, Emerging Markets, CTA, dossier