Document Quality Associate

Document Quality Associate role at Resolian UK.

• Have a good knowledge of, and perform regulated studies to the appropriate GLP/GCP standards and latest regulatory guidelines.
• Be familiar with, and work in accordance with, SOPs and Study Documents.
• Complete all paperwork in compliance with good record keeping principles; correctly and on time with GLP/GCP.
• QC check the reports to a consistent and high standard including reviewing study files against standard check‑lists.
• Accurately communicate findings identified during QC check.
• Make suggestions to improve processes and maximise efficiency.
• Take an interest in personal development, seek training, and look for growth opportunities.
• Embrace Resolian values and be respectful to colleagues.
• Be flexible; respond positively to changing priorities and timelines.
• Take responsibility for daily tasks and complete them promptly.
• Familiarise yourself with, and adhere to, the Health and Safety policy, paying particular attention to COSHH in the lab.
• Complete any mandatory training appropriate for role.
• Have a good knowledge of QC checking reports (documents, data, tables) produced within IA and LCMS Bioanalysis departments.
• Understand how to QC check sample management documentation.
• Use Watson LIMS and ResoLIMS to QC check report text, tables and figures.
• Focus on quality and detail with meticulous QC checking.
• Communicate with Report Writers and SD/PI/APMs to provide updates on QC progress and update SharePoint and the Team forum appropriately.
• Liaise with relevant SD/PI/APM and/or Report Writer for further discussion.
• Work with QA to discuss audit findings and develop clarity on requirements, leading to enhanced efficiency.
• Communicate workload to line manager and ensure manageable daily workload.
• Work with the QC team to provide coverage for others as needed.
• Look for opportunities outside of core role and contribute without affecting day‑to‑day responsibilities.

• Solid knowledge of reviewing QC documents, data and data tables.
• Solid knowledge of GLP/GCP regulations.
• Strong Watson/LIMS experience.

Entry level | Full‑time | Quality Assurance