Regulatory Manager - CMC biologics (various European locations)

Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations.

As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.

Primary Tasks & Responsibilities:

• Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports.
  
• Assess change controls and provide regulatory assessments of quality changes in production and quality control.
  
• Review study reports from the quality control and production departments to ensure compliance with regulatory requirements.
  
• Coordinate submission preparation with various departments including manufacturing, supply chain, quality control and quality assurance, and other regulatory departments and local companies.
  
• Write and/or review submission content to ensure alignment with regulatory requirements, specifically related to variations and questions from health authorities.
  
• Manage projects within all Regulatory Information Management systems, ensuring the maintenance of worldwide submissions.
  
• Identify, escalate, and mitigate risks associated with regulatory procedures and activities.
  

Experience and Knowledge Requirements:

• University-level education, preferably in Life Sciences, or equivalent by experience.
  
• Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
  
• Strong understanding of CMC and post-approval regulatory requirements.
  
• Experience in writing CMC (technical) sections of regulatory documents such as registration files or variations.
  
• Knowledge of biological processes.
  
• Background in validation/Quality Assurance/production in the pharmaceutical industry, with experience in preparing regulatory documentation. Understanding of qualification/validation principles.
  
• Proficiency in Word, PowerPoint, Excel, and experience with Veeva Vault is valued.
  
• Team spirit, flexibility, accountability, and organizational skills.
  
• Fluent in English (written and spoken). French, Italian and German would be a strong plus.
  

Location: Uxbridge, GB

Posted Date: 11/23/2024