Senior Manager Regulatory Affairs

Overview

G&L have an opportunity for a senior Regulatory professional with a strong background in CMC and biotechnology. Our UK team, based in West London, has a number of projects with requirements in the coming months. Our projects are diverse and we are considering all regulatory talent for upcoming openings, including biotechnology and pharmaceutical, development and approved products.

As a G&L consultant, you will be working with a variety of clients. Your duties may include the following :

Responsibilities

• Developing submission strategies and planning for post-approval CMC activities, including variations, renewals, market expansions, and annual reports.
• Evaluating change controls and providing regulatory assessments to classify quality changes in production and quality control.
• Supporting client project teams in the preparation of the CMC sections of all submission content to facilitate approvals and continued compliance.
• Reviewing key study reports (e.g., process validation, stability studies, analytical method validation) to ensure regulatory compliance.
• Developing and maintaining high quality, realistic Chemistry, Manufacturing & Control (CMC) plans for products in development.
• CMC authoring of Module 2.3 and Module 3 sections of the CTD dossier.
• Maintaining a positive and productive liaison with internal and external contacts, including clients, regulatory agencies, and related institutions.
• Attending formal interactions (face-to-face meetings, teleconferences) with clients and, possibly, government agencies; building positive working relationships with clients.
• Identifying gaps and risks in the CMC plans and working with the team to proactively develop solutions to increase efficiency and minimize timelines.
• Assisting in the development of assessments and strategic regulatory plans for client product development programs.
• Reviewing CMC sections of BLA submissions and preparing gap analyses detailing requirements for submission to different jurisdictions.
• Participating in project teams and advising other departments on CMC regulatory issues and strategies, including manufacturing, supply chain, quality control, quality assurance, and other regulatory and local entities.

Person specification

How to apply

If you would be interested in joining the team at G&L Scientific, please send your CV to today.

G&L Scientific is an equal opportunities employer and welcomes applicants from all sections of the community regardless of gender, religious belief, political opinion, sexual orientation, disability, age, marital status or race. We recruit based on talent alone and firmly believe that an individual’s background should play no part in the recruitment and selection process.

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