Docuvera Regulatory Specialist — Submissions & Compliance

Harrington Recruitment; Greater London; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A recruitment agency is seeking a Docuvera Specialist for Regulatory Affairs support. The role requires experience with Docuvera in a pharmaceutical setting and involves creating and managing regulatory documents. Key responsibilities include ensuring compliance with regulatory standards and collaborating with various teams. This position is hybrid and based in the UK, supporting GSK indirectly through a partner organization, which entails a strong focus on quality and regulatory compliance.

Qualifications

• Proven hands‑on experience with Docuvera in a pharmaceutical regulatory environment.
• Strong understanding of CTD/eCTD structure and publishing requirements.
• Experience supporting submissions to MHRA, EMA, and/or FDA.

Responsibilities

• Create, format, manage, and maintain regulatory documents using Docuvera.
• Support preparation and lifecycle management of regulatory documentation.
• Ensure compliance with regulatory authority requirements.

Skills

Experience with Docuvera

Regulatory documentation standards

Knowledge of GxP

Document formatting skills

Communication skills in English

Education

Degree in scientific or life sciences discipline

Formal training in regulatory affairs

Job description

A recruitment agency is seeking a Docuvera Specialist for Regulatory Affairs support. The role requires experience with Docuvera in a pharmaceutical setting and involves creating and managing regulatory documents. Key responsibilities include ensuring compliance with regulatory standards and collaborating with various teams. This position is hybrid and based in the UK, supporting GSK indirectly through a partner organization, which entails a strong focus on quality and regulatory compliance.