Company: Select OH
An excellent opportunity has arisen for a Regulatory Affairs Executive to join my client based in Berkshire and focusing on cGMP, solid dosage generic pharmaceuticals. Responsibilities: Prepare and submit applications of reliable quality in a timely manner to MHRA (UK) via National Procedure. These include new licence applications, variations (including grouping and work sharing), renewals, [...]Read More... from Regulatory Affairs Executive See details
An excellent opportunity has arisen for a Regulatory Affairs Executive to join my client based in Berkshire and focusing on cGMP, solid dosage generic pharmaceuticals. Responsibilities: Prepare and submit applications of reliable quality in a timely manner to MHRA (UK) via National Procedure. These include new licence applications, variations (including grouping and work sharing), renewals, [...]Read More... from Regulatory Affairs Executive See details
An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses. Responsibilities: Primarily responsible for post-approval and compliance activities with a support role for the pre-approval team. Have an excellent understanding of and be able to execute activities [...]Read More... from Regulatory Affairs Manager See details
Responsible for collecting, organising, and tracking of documentation required for Marketing Authorisation application and response to questions in eCTD format. Check documents for accuracy, consistency, deficiencies, and compliance with regulatory submission requirements Compile module 1-5 CTD registration package for new Marketing Authorisation submissions. Submit necessary applications through ele… JBLK1_UKTJ [...]Read More... from Deputy Regulatory Manager See details
An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses. Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV. Responsibilities: Primarily responsible for post-approval [...]Read More... from Regulatory Affairs Manager See details
An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses. Responsibilities: Primarily responsible for post-approval and compliance activities with a support role for the pre-approval team. Have an excellent understanding of and be able to execute activities [...]Read More... from Regulatory Affairs Manager See details
An excellent opportunity has arisen for a Regulatory Affairs Executive to join my client based in Berkshire and focusing on cGMP, solid dosage generic pharmaceuticals. Responsibilities: Prepare and submit applications of reliable quality in a timely manner to MHRA (UK) via National Procedure. These include new licence applications, variations (including grouping and work sharing), renewals, [...]Read More... from Regulatory Affairs Executive See details
