Technical Publisher
CV-LibrarySandwich, KentcontractPosted: 18 June 2026
Apply NowTechnical 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
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