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.
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.
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.
A specialist, international Pharmaceutical company is actively seeking a Regulatory Affairs Manager due to their successful company growth and dedication to innovate new products.
The role reports directly to the Head of Regulatory Affairs and is responsible for pre-approval regulatory activities that support the delivery of the company's strategic plans.
This is an excellent opportunity to work across a number of product ranges in a growing company that is expanding globally with a focus on delivering medicines to the paediatric market.
A world leading Chemical company is looking for a Product Safety Assistant to join their team based in the Duxford.
Reporting into the Head of R&D, the successful applicant will bring knowledge of chemical regulations from the chemical industry to support the ongoing development of products.
As the Product Safety Assistant you will be
Conduct hazard classification and author Safety Data Sheets to meet global regulatory standards (GHS) and country-specific regulations.
A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team.
You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products.
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.
A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team.
You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products.
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.
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 Validation to join the QC Technical Services Team on a contract basis.
The duration of the contract will be 23 months with a start date in July or August 2024.