Regulatory review and approval and advertising or promotional copy for Cosmetics and other non-OTC classes mainly in UK & Ireland.
Support the Regulatory team with specific tasks per the needs of the department, which may include claims tracker updates, databases, compliance tasks.
Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the company portfolio in mainly UK & Ireland.
Our client is a global biotechnology company specialising in the development of immunological products to diagnose and monitor patients with immunologically controlled diseases.
The role
An opportunity has become available for an Regulatory Specialist, experienced in Diagnostics, to join company and support the Global Regulatory activities in order to facilitate timely approval of new and existing products.
We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products.
The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe.
You will grow and maintain major portfolio in particular for the European region, you will coordinate changes to existing products/dossiers keeping them on the market.
The Group Compliance Function's aim is to proactively support Willis Towers Watson to generate sustainable value, helping the company to deliver good client outcomes, manage its conduct, protect against regulatory risk, and to maintain strong regulatory relationships.
We aim to be a trusted partner to the business.
Within Willis Towers Watson's internal control system, we form part of the Second Line of Defence, as a function independent from daily business activities.
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.
The Role
The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials.
They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes.
We are currently recruiting for two Regulatory Specialists to join a Milton Keynes based company, in a 1-year fixed term contract.
Overview
You will need to:.
The successful candidate will support internal customers including: Customer Service team, Sales reps, Research & Development team, and Quality Assurance team by serving as an expert in assigned areas.
The economic regulation team provides a crucial advisory service to the rest of the business.
New joiners to the team will be given on the job training and support to help them thrive in a demanding and fast paced environment where you will be asked to provide innovative and creative insights into regulatory issues that go to the heart of how we structure our business and deliver services to customers.
You will work with cross functional teams in order to successfully execute a varied project portfolio.