Senior Regulatory Affairs Officer – EU Life Sciences

Quanta part of QCS Staffing; Greater London; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical organization based in London is seeking a Principle Registration Officer to manage regulatory authorisations for both EU and non-EU territories. The ideal candidate will have over 5 years of experience in EU Regulatory Affairs and a BSc in Life Sciences. Responsibilities include managing marketing authorisations, overseeing the DCP / MRP process, and providing support and mentoring to junior team members. A flexible approach and excellent communication skills are essential for success in this role.

Qualifications

• Minimum 5 years experience in product registrations and regulatory compliance.
• Proven ability to manage product portfolios in a fast-paced environment.
• In-depth knowledge of DCP / MRP processes.

Responsibilities

• Obtain and maintain marketing authorisations for products.
• Manage DCP / MRP process and launch meetings.
• Maintain databases according to regulatory obligations.
• Advise management on project status and compliance.
• Provide specialist knowledge and mentoring to the team.

Skills

Extensive experience in EU Regulatory Affairs

Effective communication skills

Experience in managing large product portfolios

Mentoring junior team members

Education

BSc in Life Sciences or higher

Job description

A leading pharmaceutical organization based in London is seeking a Principle Registration Officer to manage regulatory authorisations for both EU and non-EU territories. The ideal candidate will have over 5 years of experience in EU Regulatory Affairs and a BSc in Life Sciences. Responsibilities include managing marketing authorisations, overseeing the DCP / MRP process, and providing support and mentoring to junior team members. A flexible approach and excellent communication skills are essential for success in this role.