Senior DAQ Advisor

Senior DAQ Advisor

Full-Time 50000 - 65000 £ / year (est.) No working from home possible
Medicines and Healthcare Products Regulatory Agency

At a Glance

  • Tasks: Mentor and train colleagues while ensuring quality standards in data assurance.
  • Company: Join a leading health quality and access group in Canary Wharf.
  • Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
  • Other info: Dynamic role with a focus on quality and performance in a target-driven environment.
  • Why this job: Make a real impact in the health sector with your expertise in regulatory validation.
  • Qualifications: Life Sciences degree and strong organisational skills required.

The predicted salary is between 50000 - 65000 £ per year.

  • 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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Senior DAQ Advisor employer: Medicines and Healthcare Products Regulatory Agency

The Medicines and Healthcare products Regulatory Agency (MHRA) is an exceptional employer, offering a dynamic work environment in the heart of Canary Wharf, London. With a strong commitment to employee growth, the agency provides opportunities for professional development and collaboration with leading experts in healthcare and research. The hybrid working model promotes a healthy work-life balance, while the agency's focus on innovation and public health ensures that employees contribute to meaningful projects that enhance the well-being of millions.

Medicines and Healthcare Products Regulatory Agency

Contact Details:

Medicines and Healthcare Products Regulatory Agency Recruitment Team

We think you need these skills to ace Senior DAQ Advisor

Regulatory Validation
Information Management
Mentoring
Training
Quality Assurance
Communication Skills
Organisational Skills