Job Description

Technical Publisher

Overview

We are seeking a Technical Publisher to join a global regulatory operations team, supporting the delivery of high-quality regulatory submissions to both national and international markets. This is an entry-level opportunity with full training provided, offering clear exposure to regulatory publishing processes that directly enable health authority approvals and patient access to medicines worldwide.

Key Responsibilities

* Support publishing activities, ensuring all outputs are accurate, compliant, and delivered to tight deadlines

* Collaborate with internal stakeholders to ensure efficient and consistent delivery across the publishing portfolio

* Assist in the implementation of digital tools and systems to enhance publishing efficiency and workflow automation

* Contribute to system testing and validation activities to ensure functionality and regulatory compliance

* Support the rollout of new solutions, ensuring smooth integration into existing processes

* Maintain and update documentation to reflect system changes, support training, and drive user adoption

Requirements

* Strong attention to detail, with the ability to manage and review technical documentation accurately

* Excellent organisational skills and the ability to work to challenging deadlines

* Strong communication and collaboration skills

* A genuine interest in the pharmaceutical or life sciences industry, with a willingness to learn

* Comfortable working within structured, compliance-driven environments

Previous pharmaceutical experience is not required.

Training & Development

Full training will be provided. Candidates should demonstrate curiosity and a proactive approach to learning, particularly around:

* eCTD / CTD regulatory submission formats

* Regulatory publishing processes