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Document Controller

Job in Dinnington, South Yorkshire, TA17, England, UK
Listing for: Alliance Medical
Full Time position
Listed on 2026-07-31
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 28000 - 40000 GBP Yearly GBP 28000.00 40000.00 YEAR
Job Description & How to Apply Below

Due to significant expansion, we have a fantastic opportunity for a Document Controller to join our Radiopharmacy Quality team. If you have experience in Document Control within a GMP environment, an excellent grasp of Microsoft Office programs, top‑class typing and report writing skills, a time‑oriented approach to handling queries and tasks, and detail‑focused document organizing abilities, then this may be the opportunity you are looking for.

The Document Controller will be an active member of the Quality Assurance Team, responsible for supporting the QA Manager in managing the QA Document Control System and tracking training compliance to ensure the site complies with quality objectives, company procedures and regulatory requirements.

The QA department oversees GMP compliance and the effectiveness of the Quality Management Systems supporting the manufacturing, testing and release of the product. Prior experience within a radiopharmaceutical setting is desirable; experience in Good Manufacturing Practice (GMP) is essential.

The hours of work for the role are 40 hours per week, Monday to Friday.

Our benefits include 5 weeks holiday, discounted private health insurance and a pension plan.

Alliance Medical is committed to ensuring that recruitment and selection practices are conducted in a manner that promotes equality of opportunity.

Please note that we will be interviewing throughout the duration of this advert. Therefore, if you are interested in this role an early application is advised as we may close the advert prior to the advertised date.

Qualifications
  • GCSEs (or equivalent qualification) in English and Math's.
  • Preferably, experience in Document control within a GMP Quality Assurance environment.
  • An excellent grasp of Microsoft Office programs.
  • Top‑class typing and report writing skills.
  • Time‑oriented approach to handling queries and tasks.
  • Focused document organizing abilities.
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