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.
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.
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, UK/IE 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.
We are searching for a Regulatory Associate on a long term temporary basis, to provide key regulatory admin support within the Regulatory Team of an established manufacturing client in the area.
Previous administrative experience gained within a regulated environment is desirable, ie.
The role has become available as a result of a continuing increase in workload.
You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products.
A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team.
This is a great opportunity to work with a team who take provide in working to the highest standards, passionate about delivering excellence and focused on sharing regulatory best practice and guidance throughout the wider business.
Support the Regulatory Team and distributors in EMEA regions to provide timely submissions in support of new and marketed products.
General
Working cross-functionally with Commercial/Sales, Marketing and R&D you will be responsible for tracking and coordinating registration activities and providing support for regulatory submission activities.
Working for a global manufacturing company in the Folkestone area, we are resourcing for a Regulatory Associate who will be supporting regulatory processes and has potential to lead on small projects.
A key role in the execution of CMC regulatory strategies working on multiple cross functional projects.
General
Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract.
This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science.
I am recruiting an experienced Commercial Policy and Compliance Officer on a temporary basis for 9-12 months to work for a Local Authority in London.
The expectation would be for you to work 2-3 days on-site in Central London and 1 day from home.The purpose of the role will be to support the Commercial Director in the provision of overall strategic support, development and planning for Commercial Services and the wider authority's business.
This is a fantastic opportunity to work on a high-profile programme in a fast-paced, friendly and supportive team.