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Senior DAQ Advisor

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: Medicines and Healthcare products Regulatory Agency
Full Time position
Listed on 2026-07-17
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 55000 - 75000 GBP Yearly GBP 55000.00 75000.00 YEAR
Job Description & How to Apply Below
Location: Greater London

We are currently looking for a Senior DAQ Advisor to join our DAQ Variations Function within the Health Quality and Access group.

Position:
Full‑time, Permanent
.

Location:

10 South Colonnade, Canary Wharf, London, E14 4PU
.

The role is part of a hybrid work arrangement with a minimum of 8 days per month onsite, subject to business needs.

Overview

Senior DAQ Advisors play a vital role in supporting their colleagues through mentoring and training, providing day‑to‑day support for Delivery Leads, and ensuring performance and quality standards are met across the Data Assurance & Quality (DAQ) functions. They apply their specialist knowledge in regulatory validation and information management for variations, new MAA, and clinical trial submissions.

The position operates in a target‑driven environment where speed, quality and consistency are paramount and requires confident communication with both internal teams and external applicants.

Key Responsibilities
  • Work closely with the Delivery Lead to ensure service‑level and legislative targets are met.
  • Provide expertise with work procedures and processes across all work areas, including complex procedures such as variations, new MAA and electronic submission formats.
  • Ensure regulatory guidelines are followed in checking the validity of received applications.
  • Support and assist DAQ Classifiers in preparing high‑quality case folders for professional assessment, allocating them to the relevant agency function within required time‑scales and targets.
  • Mentor and train classifiers within the unit to help ensure performance and quality standards are achieved.
Qualifications
  • Change and improve processes and outcomes.
  • Manage a quality service, delivering on deadlines in a target‑driven environment.
  • Graduate with a Life Sciences degree or other relevant degree.
  • Proven organisational skills and ability to work to deadlines.
  • Demonstrated knowledge of regulatory procedures surrounding the licensing of medicinal products in the UK and Europe.
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Position Requirements
10+ Years work experience
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