Document Controller

15391ContractCompetitiveSite BasedLondon - United KingdomUpdated on: 13-03-2026

We are currently recruiting a Document Controller to join a leading Pharmaceutical company based in the Hertfordshire area. This is an exciting opportunity for a detail-oriented professional to support automation engineering projects within a dynamic environment. The role offers a chance to work on critical documentation, ensuring compliance and accuracy throughout project lifecycles.

This role is ideal for someone experienced in document management within GMP, manufacturing, or other process-driven sectors. Our client is looking for a proactive individual who can effectively support their automation initiatives for an initial 12-month period.

KEY DUTIES AND RESPONSIBILITIES
Your duties as the Document Controller will be varied however the key duties and responsibilities are as follows:

As the Document Controller, you will manage and control project documentation, including GMP, installation, and project-related documents, ensuring document accuracy, version control, and timely updates.
As the Document Controller, you will support automation projects by organizing and maintaining relevant documentation in line with compliance standards.
As the Document Controller, you will liaise effectively with project teams, providing document support and ensuring all documentation meets industry and regulatory requirements.
As the Document Controller, you will ensure all project records are correctly stored and accessible as required.
As the Document Controller, you will be responsible for supporting the integrity and compliance of project documentation throughout the project lifecycle.

ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Document Controller we are looking to identify the following on your profile and past history:

A Degree or higher level in a relevant field (e.g., Life Sciences, Engineering, Quality Assurance, or Document Management).
Proven experience in document control within regulated or process industries, with a good understanding of GMP or ISO standards.
Strong organizational skills with the ability to manage multiple documentation processes efficiently.
Excellent communication skills to liaise with project teams and stakeholders effectively.
As the Document Controller you will be able to work onsite full-time and adapt quickly to project needs.

WHAT’S IN IT FOR YOU?

Full-time onsite work for the duration of the assignment
Opportunity to support or lead automation projects across regulated industries
The chance to develop your experience within dynamic and compliant environments

Key Words: Document Control / GMP / Project Documentation / Automation / Regulated Industries / Onsite / Contract / Compliance / Document Controller / Engineering Controller / Engineering Control / Project Controls / Pharma / Pharmaceutical / Biotech / Biotechnology / COMAH / Chemical / Oil and Gas / Petrochemical / FMCG / Food

"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.