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.
An exciting opportunity has arisen to appoint a new Temporary Administrative Officer for the Information Governance Team, within the Service Performance and Communications Department, South Wales Fire and Rescue Service Headquarters, Forest View Business Park, Llantrisant, CF72 8LX.
The successful applicant will provide administrative support to the Information Governance Manager in matters relating to Information Governance, ensuring compliance with the relevant legislation.
Our client, a regulatory organisation overseeing the optical professions in the UK, is currently seeking a highly skilled and dynamic Operations Manager (Investigations) to join their team.
As the Operations Manager, you will lead and manage a team of caseworkers and administrators within the Regulatory Operations directorate, ensuring that all fitness to practise (FtP) investigations are handled promptly, proportionately, and appropriately.
Pay £185.10 per day, start ASAP, duration for three months, this is an interim role, hours Mon-Fri 34.75 hours per week, this is a hybrid working role and you will be required to work in the office two days a week,
You will be responsible for scheduling Dispatch resources to meet the demand of customer driven emergency workload within Cadent Networks.
We are looking for an enthusiastic individual to join our Workforce Management team.
General
Reed Talent Solutions are working with Cadent Gas on the search for Workforce Management Administrator to join their fast-paced Workforce Management team.
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved.
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract.
Other responsibilities include
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
This opportunity is for a Senior QC Analyst to join the QC Technical Services Team on a contract basis.
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