Document Controller

QCS Staffing • Biotechnology • 12-month contract • Master's Degree • 3 days ago
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Salary
≈ $37k – $87k per year (Estimated)
Location
In office (Liverpool)
Employment
Contractor

Confirmed on the employer's own hiring board on Oct 24, 2026. First seen by Alion on Jun 18, 2026. QCS Staffing scores A on the Alion truth index.

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QCS Staffing

QCS Staffing, formerly Quanta Consultancy Services, is a specialist recruitment agency headquartered in Berkhamsted, Hertfordshire, that places contractors, permanent staff and executives in life sciences, data centres, IT, renewable energy and heavy lift. Founded in 1992, it has worked for clients in more than 30 countries and runs offices in the UK, the United States, Ireland, Puerto Rico and the Netherlands, including one in Research Triangle Park, North Carolina. Its assignments include project, process, CQV and automation engineers, construction and electrical design managers, procurement advisers and network engineers on client capital projects.
qcsstaffing.com • HQ: Berkhamsted, United Kingdom • Recruiting & Staffing • 1-10 employees • Est. 1992
Document Controller - UK, Liverpool - 12 Month Contract Our client is a global biopharmaceutical company manufacturing plasma-derived, and recombination therapeutic products, who in turn deliver high-quality medicines that treat people with rare and serious diseases, and we are now searching on an exclusive basis with the client to appoint a Document Controller to join their busy and rewarding team on a contractual basis for a period of 12 months.What you'll do:

Support globally aligned document administration in the electronic Document Management System(s) (DMS), by executing various document management tasks within the DMS.This role also provides support for paper and electronic records management and archival, according to applicable processes and within the relevant electronic systems.

What you'll need:

Extensive experience in the pharmaceutical/biotech industry, or other highly regulated industry.Proficiency in MS office and other software programs.Knowledge of cGMP/GXP standardsGood attention to detailStrong communication and interpersonal skills, with the ability to collaborate effectively with diverse stakeholders.

If this role is of interest, please apply now!#LI-BA1

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