I am exclusively working with an established name within the Asset Management space to bring on an experienced Regulatory Reporting specialist.
Due to an internal secondment, this role serves as a backfill into the BAU Group Regulatory team, where you will have end to end responsibility for the financial data under your management.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
The duration of the contract will be 23 months with a start date in July or August 2024.
This opportunity is for a Senior QC Analyst Validation to join the QC Technical Services Team on a contract basis.
Posted by Randstad Construction & Property • £12.75/hr
Start Time: Between 7:30 AM to 8:30 AM
About the Role: In this role, you will provide technical support and process operation for the Process Research and Development team.
You will work as part of a team in a laboratory setting, supporting chemists and engineers, and ensuring the smooth and safe execution of laboratory work.
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.
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.
Conduct hazard classification and author Safety Data Sheets to meet global regulatory standards (GHS) and country-specific regulations.
General
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.
A world leading Chemical company is looking for a Product Safety Assistant to join their team based in the Duxford.